Verfügbarkeit: CO2 as a building block in organic synthesis

CO2 as a building block in organic synthesis:

Gespeichert in:

Bibliographische Detailangaben
Weitere Verfasser:	Das, Shoubhik 1980- (HerausgeberIn)
Format:	Buch
Sprache:	English
Veröffentlicht:	Weinheim Wiley-VCH [2020]
Schlagworte:	Kohlendioxid Carboxylierung Anorganische Chemie Chemie Chemistry CO2 Inorganic Chemistry Methods - Synthesis & Techniques Organische Chemie / Methoden, Synthesen, Verfahren Pharmaceutical & Medicinal Chemistry Pharmazeutische u. Medizinische Chemie CH60: Pharmazeutische u. Medizinische Chemie CH70: Anorganische Chemie CH81: Organische Chemie / Methoden, Synthesen, Verfahren Aufsatzsammlung
Online-Zugang:	http://www.wiley-vch.de/publish/dt/books/ISBN978-3-527-34613-4/ Inhaltsverzeichnis
Beschreibung:	Die 2 im Titel ist tiefgestellt
Beschreibung:	x, 453 Seiten Illustrationen
ISBN:	9783527346134

Internformat

MARC


LEADER	00000nam a2200000 c 4500
001	BV046885778
003	DE-604
005	20211124
007	t
008	200907s2020 gw a\|\|\| \|\|\|\| 00\|\|\| eng d
016	7		\|a 1207012084 \|2 DE-101
020			\|a 9783527346134 \|9 978-3-527-34613-4
035			\|a (OCoLC)1289788406
035			\|a (DE-599)DNB1207012084
040			\|a DE-604 \|b ger \|e rda
041	0		\|a eng
044			\|a gw \|c XA-DE-BW
049			\|a DE-11 \|a DE-29T \|a DE-19
084			\|a VK 5500 \|0 (DE-625)147401:253 \|2 rvk
084			\|a VK 6000 \|0 (DE-625)147413:253 \|2 rvk
245	1	0	\|a CO2 as a building block in organic synthesis \|c edited by Shoubhik Das
264		1	\|a Weinheim \|b Wiley-VCH \|c [2020]
264		4	\|c © 2020
300			\|a x, 453 Seiten \|b Illustrationen
336			\|b txt \|2 rdacontent
337			\|b n \|2 rdamedia
338			\|b nc \|2 rdacarrier
500			\|a Die 2 im Titel ist tiefgestellt
650	0	7	\|a Kohlendioxid \|0 (DE-588)4031648-8 \|2 gnd \|9 rswk-swf
650	0	7	\|a Carboxylierung \|0 (DE-588)4205211-7 \|2 gnd \|9 rswk-swf
653			\|a Anorganische Chemie
653			\|a Chemie
653			\|a Chemistry
653			\|a CO2
653			\|a Inorganic Chemistry
653			\|a Kohlendioxid
653			\|a Methods - Synthesis & Techniques
653			\|a Organische Chemie / Methoden, Synthesen, Verfahren
653			\|a Pharmaceutical & Medicinal Chemistry
653			\|a Pharmazeutische u. Medizinische Chemie
653			\|a CH60: Pharmazeutische u. Medizinische Chemie
653			\|a CH70: Anorganische Chemie
653			\|a CH81: Organische Chemie / Methoden, Synthesen, Verfahren
655		7	\|0 (DE-588)4143413-4 \|a Aufsatzsammlung \|2 gnd-content
689	0	0	\|a Kohlendioxid \|0 (DE-588)4031648-8 \|D s
689	0	1	\|a Carboxylierung \|0 (DE-588)4205211-7 \|D s
689	0		\|5 DE-604
700	1		\|a Das, Shoubhik \|d 1980- \|0 (DE-588)1018978429 \|4 edt
710	2		\|a Wiley-VCH \|0 (DE-588)16179388-5 \|4 pbl
776	0	8	\|i Erscheint auch als \|n Online-Ausgabe, PDF \|z 978-3-527-82194-5
776	0	8	\|i Erscheint auch als \|n Online-Ausgabe, EPUB \|z 978-3-527-82196-9
776	0	8	\|i Erscheint auch als \|n Online-Ausgabe, OBOOK \|z 978-3-527-82195-2
856	4	2	\|m X:MVB \|u http://www.wiley-vch.de/publish/dt/books/ISBN978-3-527-34613-4/
856	4	2	\|m DNB Datenaustausch \|q application/pdf \|u http://bvbr.bib-bvb.de:8991/F?func=service&doc_library=BVB01&local_base=BVB01&doc_number=032295695&sequence=000001&line_number=0001&func_code=DB_RECORDS&service_type=MEDIA \|3 Inhaltsverzeichnis
999			\|a oai:aleph.bib-bvb.de:BVB01-032295695

Datensatz im Suchindex

_version_	1804181746752684032
adam_text	CONTENTS 1 PHOTOCHEMICAL AND SUBSTRATE-DRIVEN CO 2 CONVERSION 1 BART LIMBURG, CRISTINA MAQUILON, AND ARJAN W. KLEIJ 1.1 1.2 1.3 INTRODUCTION 1 IODINE ACTIVATION OF (HOMO)ALLYLIC SUBSTRATES 3 SUBSTRATE ACTIVATION VIA RADICAL ADDITION/PHOTOCHEMICAL OXIDATION PROCESSES 9 1.4 1.5 1.6 SUBSTRATE-INDUCED ACTIVATION OF OXIRANES 12 SUBSTRATE-INVOLVED ACTIVATION OF OXETANES AND AZETIDINES 21 CONCLUDING REMARKS 21 REFERENCES 22 2 C-H CARBOXYLATIONS WITH CO 2 29 UTTAM DHAWA, ISAAC CHOI, AND LUTZ ACKERMANN 2.1 2.2 2.2.1 2.2.2 2.2.3 2.2.4 2.2.5 2.2.6 2.2.7 2.2.8 2.2.9 2.2.10 2.2.11 2.3 2.3.1 2.3.2 2.3.3 2.3.4 2.4 2.5 INTRODUCTION 29 TRANSITION-METAL-CATALYZED C-H CARBOXYLATION 30 COPPER-CATALYZED C-H CARBOXYLATION 30 COBALT-CATALYZED C-H CARBOXYLATION 36 NICKEL-CATALYZED C-H CARBOXYLATION 36 MOLYBDENUM-CATALYZED C-H CARBOXYLATION 38 RUTHENIUM-CATALYZED C-H CARBOXYLATION 38 RHODIUM-CATALYZED C-H CARBOXYLATION 39 PALLADIUM-CATALYZED C-H CARBOXYLATION 41 SILVER-CATALYZED C-H CARBOXYLATION 42 IRIDIUM-CATALYZED C-H CARBOXYLATION 45 GOLD-CATALYZED C-H CARBOXYLATION 45 NEODYMIUM-CATALYZED C-H CARBOXYLATION 45 METAL-FREE C-H CARBOXYLATION 46 BASE-MEDIATED C-H CARBOXYLATION 46 ELECTRO-CATALYZED C-H CARBOXYLATION 49 LEWIS ACID-MEDIATED CARBOXYLATION 49 LIGHT-DRIVEN CARBOXYLATION 50 CO 2 CARBOXYLATION PROMOTED BY TRANSITION METAL COMPLEXES 52 CONCLUSIONS 53 REFERENCES 53 VI 3 TRANSITION-METAL-CATALYZED C-H CARBOXYLATION 59 JOAQUIM CAN ER AND NOBUHARU IWASAWA 3.1 INTRODUCTION 59 3.2 DIRECT C-H CARBOXYLATION OF ELECTRON-DEFICIENT ARENES AND (HETERO) ARENES CATALYZED BY BASIC COMPLEXES 59 3.3 DIRECT CARBOXYLATION OF INERT CSP 2 H BONDS 66 3.3.1 RHODIUM-CATALYZED C-H CARBOXYLATION REACTIONS 66 3.3.2 PALLADIUM-CATALYZED C-H CARBOXYLATION REACTIONS 76 3.4 DIRECT CARBOXYLATION OF CSP 3 - H BONDS 85 3.5 SUMMARY AND OUTLOOK 89 REFERENCES 90 4 FIXATION OF CO 2 IN ORGANIC MOLECULES WITH HETEROGENEOUS CATALYSTS 95 DONGCHENG HE, HONGLI WANG, AND FENG SHI 4.1 INTRODUCTION 95 4.2 CO 2 CYCLOADDITION TO EPOXIDE 96 4.2.1 OXIDES 96 4.2.2 ZEOLITE CATALYSTS 97 4.2.3 SUPPORTED NANOPARTICLE AND LEWIS ACID CATALYSTS 98 4.2.4 CARBON AND ITS DERIVATIVES 99 4.2.5 SALEN, PORPHYRIN, AND PHTHALOCYANINE CATALYST 101 4.2.6 IONIC LIQUID CATALYST 103 4.2.7 METAL-ORGANIC FRAMEWORK (MOF) CATALYST 108 4.2.8 BIFUNCTIONAL CATALYST 112 4.2.9 OTHER CATALYSTS 120 4.3 REACTIONS OF AZIRIDINES AND CO2 120 4.4 REACTIONS OF POLYALCOHOLS/OLEFINS AND CO2 121 4.5 REACTION OF PROPARGYL ALCOHOLS/PROPARGYL AMINES AND CO 2 124 4.6 REACTIONS OF TERMINAL ALKYNES AND CO2 125 4.7 FORMYLATION OF AMINES AND CO2 127 4.8 METHYLATION OF AMINES AND CO2 130 4.9 OTHER REACTIONS OF AMINES AND CO2 131 4.10 HYDROFORMYLATION OF CO2 AND OLEFINS INTO ALCOHOLS 133 4.11 REACTIONS OF AROMATIC HALIDES AND CO2 134 4.12 REACTIONS OF 2 AMINOBENZONITRILES AND CO2 136 4.13 CONCLUSIONS 137 REFERENCES 138 5 CO 2 FIXATION INTO ORGANIC MOLECULES VIA CARBON-HETEROATOM BOND FORMATION 155 YU-NONG LI, HONG-RU LI AND LIANG-NIAN HE 5.1 INTRODUCTION 155 5.2 CO2 CONVERSION WITH C - N BOND FORMATION 157 5.2.1 SYNTHESIS OF OXAZOLIDINONES 157 5.2.1.1 OXAZOLIDINONE SYNTHESIS FROM AZIRIDINE AND CO2 158 VII 5.2.1.2 OXAZOLIDINONE SYNTHESIS FROM OLEFIN, A NITROGEN SOURCE, ANDCO2 163 5.2.1.3 5.2.1.4 OXAZOLIDINONE SYNTHESIS FROM AMINO ALCOHOLS AND CO2 164 OXAZOLIDINONE SYNTHESIS FROM CARBOXYLATIVE CYCLIZATION OF PROPARGYL AMINES WITH CO2 165 5.2.1.5 OXAZOLIDINONE SYNTHESIS FROM PROPARGYL ALCOHOL, ALIPHATIC AMINES/ 2 -AMINOETHANOLS, AND CO 2 167 5.2.1.6 PHOTOINDUCED RADICAL-INITIATED CARBOXYLATIVE CYCLIZATION OF ALLYL AMINES WITH CO2 170 5.2.2 5.2.3 5.2.4 5.3 5.3.1 5.3.1.1 5.3.1.2 SYNTHESIS OF ISOCYANATES AND LINEAR CARBAMATES 172 SYNTHESIS OF UREA DERIVATIVES 174 SYNTHESIS OF QUINAZOLINES 175 CO2 CONVERSION WITH C - O BOND FORMATION 178 SYNTHESIS OF CYCLIC CARBONATES 178 CYCLIC CARBONATE SYNTHESIS FROM EPOXIDE AND CO2 178 A-ALKYLIDENE CYCLIC CARBONATE SYNTHESIS FROM CARBOXYLATIVE CYCLIZATION OF PROPARGYL ALCOHOLS WITH CO2 181 5.3.1.3 CYCLIC CARBONATE SYNTHESIS FROM CARBOXYLATIVE CYCLIZATION OF 1,2-DIOLS WITH CO2 182 5.3.1.4 ONE-POT STEPWISE SYNTHESIS OF CYCLIC CARBONATES DIRECTLY FROM OLEFINS OR VICINAL HALOHYDRINS WITH CO2 183 5.3.2 5.4 5.4.1 5.4.2 5.4.3 5.5 SYNTHESIS OF LINEAR CARBONATES 185 CO2 CONVERSION WITH C - S BOND FORMATION 187 SYNTHESIS OF DITHIOACETALS 187 SYNTHESIS OF BENZOTHIAZOLONES 188 SYNTHESIS OF BENZOTHIAZOLES 189 CARBON-HETEROATOM BOND FORMATION FROM THE CAPTURED CO2 OR CO2 DERIVATIVES 190 5.6 CONCLUSIONS 191 ABBREVIATIONS 192 REFERENCES 193 6 CARBONYL-ENE REACTIONS OF ALKENES WITH CARBON DIOXIDE 199 YASUYUKI MORI AND MASANARI KIMURA 6.1 6.2 6.2.1 INTRODUCTION 199 CARBONYL-ENE REACTIONS OF ALKENES WITH CO2 199 ORGANOALUMINUM AND PYRIDINE DERIVATIVE-MEDIATED COUPLING REACTION 199 6.2.2 LIGHT-INDUCED COPPER-CATALYZED CARBOXYLATION OF ALLYLIC C - H BONDS 204 6.2.3 COPPER AND ALUMINUM ATE COMPOUND SYSTEM FOR CARBOXYLATION OF ALLYLIC C - H BOND OF ALKENES 208 6.2.4 COBALT-CATALYZED CARBOXYLATION OF ALLYLIC C - H BOND OF TERMINAL ALKENES 272 6.2.5 NICKEL-CATALYZED CARBONYL-ENE-TYPE REACTION OF TERMINAL ALKENES WITH CO 2 277 REFERENCES 223 VIII J 7 RECENT ADVANCES IN ELECTROCHEMICAL CARBOXYLATION OF ORGANIC COMPOUNDS FOR CO 2 VALORIZATION 225 LUCA DELL AMICO, MARCELLA BONCHIO, AND XAVIER COMPANYO 7.1 INTRODUCTION 225 7.2 ELECTROCHEMICAL CARBOXYLATION OF UNSATURATED COMPOUNDS 228 73 ELECTROCHEMICAL CARBOXYLATION OF ORGANIC HALIDES 236 7.4 STEREOSELECTIVE ELECTROCHEMICAL CARBOXYLATIONS 245 7.5 CONCLUSIONS 249 REFERENCES 250 8 PHOTOCATALYSIS AS A POWERFUL TOOL FOR THE UTILIZATION OF CO 2 IN ORGANIC SYNTHESIS 253 DANIEL RIEMER AND SHOUBHIK DAS 8.1 KEY INTERMEDIATE INVOLVING SUBSTRATE WITH LATE-STAGE CO 2 ADDITION/ INSERTION 254 8.1.1 UNSATURATED SUBSTRATES 254 8.1.2 ARYL HALIDES 264 8.1.3 BENZYLIC C - H BONDS 267 8.2 CO 2 SUBSTRATE ADDUCT AS THE KEY INTERMEDIATE 269 8.3 CO2 RADICAL ANION AS A KEY INTERMEDIATE 276 8.4 HYDROXYCARBONYL RADICAL AS A KEY INTERMEDIATE 282 8.5 CONCLUSION AND OUTLOOK 284 REFERENCES 285 9 DIRECT CARBOXYLATION OF ALKENES AND ALKYNES 291 MARTIN PICHETTE DRAPEAU, JOHANNES SCHRANCK, AND AN IS TLILI 9.1 INTRODUCTION 291 9.2 CARBOXYLATION OF ALKENES 291 9.2.1 STOICHIOMETRIC CARBOXYLATION OF ALKENES 291 9.2.2 CATALYTIC HYDROCARBOXYLATION OF ALKENES 295 9.2.3 PHOTOINDUCED HYDROCARBOXYLATION OF ALKENES 300 9.2.4 DIFUNCTIONALIZATION OF ALKENES WITH CARBON DIOXIDE 304 9.3 CARBOXYLATION OF ALKYNES 305 9.3.1 CARBOXYLATION OF TERMINAL ALKYNES 305 9.3.1.1 SYNTHESIS OF PROPIOLIC ESTERS 305 9.3.1.2 SYNTHESIS OF PROPIOLIC ACIDS 308 9.3.2 SYNTHESIS OF ACRYLIC ACID DERIVATIVES 316 9.3.2.1 HYDROCARBOXYLATION 316 93.2.2 ALKYL AND ARYLCARBOXYLATIONS 321 93,23 SILA AND BORACARBOXYLATIONS 323 9.3.3 CARBOXYLATION LEADING TO CYCLIZATION PRODUCTS 324 9.4 CONCLUSIONS 326 REFERENCES 327 IX 10 HOMOGENEOUS IRON CATALYSTS FOR THE SYNTHESIS OF USEFUL MOLECULES FROM CO 2 331 FRANCESCO DELLA MONICA AND CARMINE CAPACCHIONE 10.1 10.2 10.2.1 10.2.2 10.2.3 10.3 10.3.1 INTRODUCTION 331 REDUCTIVE PROCESSES 332 HYDROGENATION 332 HYDROSILYLATION AND HYDROBORATION 335 MECHANISTIC DETAILS 336 NONREDUCTIVE PROCESSES 337 CYCLIC ORGANIC CARBONATES AND ALIPHATIC POLYCARBONATES FROM CO 2 AND EPOXIDES 337 10.3.2 10.3.3 10.3.4 10.4 MECHANISTIC DETAILS 346 STEREOCHEMISTRY OF CYCLIC ORGANIC CARBONATES 354 OXAZOLIDINONES 358 CONCLUSIONS 360 REFERENCES 360 11 NHC-CATALYZED CO 2 FIXATIONS IN ORGANIC SYNTHESIS 367 VLSHAKHA GOYAL, NAINA SARKI, ANAND NARANI, AND KISHORE NATTE 11.1 11.2 11.2.1 11.2.2 11.2.3 11.3 11.4 11.4.1 11.4.2 11.4.3 11.4.4 11.5 11.5.1 11.5.2 11.6 11.7 INTRODUCTION 367 DIRECT C-H ACTIVATION WITH CO 2 369 C-H ACTIVATION OF TERMINAL ALKYNES 369 CARBOXYLATION OF ARENES AND HETEROARENES 373 CARBOXYLATION OF ALKENES AND ORGANOBORONIC ESTERS 376 OXIDATION OF ALDEHYDES WITH CO 2 376 CYCLIZATION REACTIONS WITH CO 2 379 SYNTHESIS OF CYCLIC CARBONATES FROM CO 2 AND EPOXIDES 379 CYCLIZATION OF CO 2 IN PRESENCE OF NHC-CO 2 ADDUCTS 380 CYCLIZATION OF CO 2 IN PRESENCE OF METAL NHCS COMPLEXES 382 CYCLIZATION OF PROPARGYLIC AMINES 385 ALKYLATION WITH CO 2 387 N-METHYLATION 387 N-FORMYLATION 388 MISCELLANEOUS 390 SUMMARY 393 REFERENCES 393 12 SILVER-CATALYZED CO 2 FIXATION 397 KODAI SAITO AND TOHRU YAMADA 12.1 12.2 INTRODUCTION 397 HISTORICAL BACKGROUND OF CARBON DIOXIDE FIXATION INTO ORGANOSILVER COMPLEXES 398 12.3 12.4 12.5 CARBOXYLATION OF TERMINAL ALKYNES 399 CASCADE CARBOXYLATIVE CYCLIZATION 404 SILVER-CATALYZED SEQUENTIAL CARBOXYLATIVE CYCLIZATION OF PROPARGYL ALCOHOLS 405 12.6 SYNTHESIS OF CYCLIC CARBONATE 405 12.7 CATALYTIC ASYMMETRIC SYNTHESIS OF CYCLIC CARBONATE 411 12.8 THREE-COMPONENT REACTION OF PROPARGYL ALCOHOLS, CARBON DIOXIDE, AND NUCLEOPHILES 411 12.9 CCVMEDIATED TRANSFORMATION OF PROPARGYL ALCOHOLS 412 12.10 TRANSFORMATION OF AMINE DERIVATIVES 417 12.11 CASCADE CARBOXYLATION AND CYCLIZATION OF UNSATURATED AMINE DERIVATIVES 417 12.11.1 BENZOXAZINE-2-ONE FROM O-ALKYNYLANILINE AND CARBON DIOXIDE 418 12.11.2 CASCADE CARBOXYLATION - ADDITION TO ALLENES 418 12.11.3 THREE-COMPONENT REACTION OF CARBON DIOXIDE, AMINES, AND ARYLOXYALLENS 419 12.12 DOMINO CARBOXYLATION - CYCLIZATION - MIGRATION OF UNSATURATED AMINES 421 12.12.1 CARBOXYLATION INVOLVING C - C BOND FORMATION - SEQUENTIAL CYCLIZATION 423 12.12.2 CARBOXYLATION OF ENOLATE - SEQUENTIAL CYCLIZATION 423 12.12.3 CARBON DIOXIDE INCORPORATION REACTION USING OTHER CARBANIONS 427 12.13 CARBOXYLATION OF ARYLBORONIC ESTERS 428 12.13.1 FUNCTIONALIZATION OF TERMINAL EPOXIDES 431 12.14 CONCLUSION 432 REFERENCES 433 INDEX 437
adam_txt	CONTENTS 1 PHOTOCHEMICAL AND SUBSTRATE-DRIVEN CO 2 CONVERSION 1 BART LIMBURG, CRISTINA MAQUILON, AND ARJAN W. KLEIJ 1.1 1.2 1.3 INTRODUCTION 1 IODINE ACTIVATION OF (HOMO)ALLYLIC SUBSTRATES 3 SUBSTRATE ACTIVATION VIA RADICAL ADDITION/PHOTOCHEMICAL OXIDATION PROCESSES 9 1.4 1.5 1.6 SUBSTRATE-INDUCED ACTIVATION OF OXIRANES 12 SUBSTRATE-INVOLVED ACTIVATION OF OXETANES AND AZETIDINES 21 CONCLUDING REMARKS 21 REFERENCES 22 2 C-H CARBOXYLATIONS WITH CO 2 29 UTTAM DHAWA, ISAAC CHOI, AND LUTZ ACKERMANN 2.1 2.2 2.2.1 2.2.2 2.2.3 2.2.4 2.2.5 2.2.6 2.2.7 2.2.8 2.2.9 2.2.10 2.2.11 2.3 2.3.1 2.3.2 2.3.3 2.3.4 2.4 2.5 INTRODUCTION 29 TRANSITION-METAL-CATALYZED C-H CARBOXYLATION 30 COPPER-CATALYZED C-H CARBOXYLATION 30 COBALT-CATALYZED C-H CARBOXYLATION 36 NICKEL-CATALYZED C-H CARBOXYLATION 36 MOLYBDENUM-CATALYZED C-H CARBOXYLATION 38 RUTHENIUM-CATALYZED C-H CARBOXYLATION 38 RHODIUM-CATALYZED C-H CARBOXYLATION 39 PALLADIUM-CATALYZED C-H CARBOXYLATION 41 SILVER-CATALYZED C-H CARBOXYLATION 42 IRIDIUM-CATALYZED C-H CARBOXYLATION 45 GOLD-CATALYZED C-H CARBOXYLATION 45 NEODYMIUM-CATALYZED C-H CARBOXYLATION 45 METAL-FREE C-H CARBOXYLATION 46 BASE-MEDIATED C-H CARBOXYLATION 46 ELECTRO-CATALYZED C-H CARBOXYLATION 49 LEWIS ACID-MEDIATED CARBOXYLATION 49 LIGHT-DRIVEN CARBOXYLATION 50 CO 2 CARBOXYLATION PROMOTED BY TRANSITION METAL COMPLEXES 52 CONCLUSIONS 53 REFERENCES 53 VI 3 TRANSITION-METAL-CATALYZED C-H CARBOXYLATION 59 JOAQUIM CAN ER AND NOBUHARU IWASAWA 3.1 INTRODUCTION 59 3.2 DIRECT C-H CARBOXYLATION OF ELECTRON-DEFICIENT ARENES AND (HETERO) ARENES CATALYZED BY BASIC COMPLEXES 59 3.3 DIRECT CARBOXYLATION OF INERT CSP 2 " H BONDS 66 3.3.1 RHODIUM-CATALYZED C-H CARBOXYLATION REACTIONS 66 3.3.2 PALLADIUM-CATALYZED C-H CARBOXYLATION REACTIONS 76 3.4 DIRECT CARBOXYLATION OF CSP 3 - H BONDS 85 3.5 SUMMARY AND OUTLOOK 89 REFERENCES 90 4 FIXATION OF CO 2 IN ORGANIC MOLECULES WITH HETEROGENEOUS CATALYSTS 95 DONGCHENG HE, HONGLI WANG, AND FENG SHI 4.1 INTRODUCTION 95 4.2 CO 2 CYCLOADDITION TO EPOXIDE 96 4.2.1 OXIDES 96 4.2.2 ZEOLITE CATALYSTS 97 4.2.3 SUPPORTED NANOPARTICLE AND LEWIS ACID CATALYSTS 98 4.2.4 CARBON AND ITS DERIVATIVES 99 4.2.5 SALEN, PORPHYRIN, AND PHTHALOCYANINE CATALYST 101 4.2.6 IONIC LIQUID CATALYST 103 4.2.7 METAL-ORGANIC FRAMEWORK (MOF) CATALYST 108 4.2.8 BIFUNCTIONAL CATALYST 112 4.2.9 OTHER CATALYSTS 120 4.3 REACTIONS OF AZIRIDINES AND CO2 120 4.4 REACTIONS OF POLYALCOHOLS/OLEFINS AND CO2 121 4.5 REACTION OF PROPARGYL ALCOHOLS/PROPARGYL AMINES AND CO 2 124 4.6 REACTIONS OF TERMINAL ALKYNES AND CO2 125 4.7 FORMYLATION OF AMINES AND CO2 127 4.8 METHYLATION OF AMINES AND CO2 130 4.9 OTHER REACTIONS OF AMINES AND CO2 131 4.10 HYDROFORMYLATION OF CO2 AND OLEFINS INTO ALCOHOLS 133 4.11 REACTIONS OF AROMATIC HALIDES AND CO2 134 4.12 REACTIONS OF 2 AMINOBENZONITRILES AND CO2 136 4.13 CONCLUSIONS 137 REFERENCES 138 5 CO 2 FIXATION INTO ORGANIC MOLECULES VIA CARBON-HETEROATOM BOND FORMATION 155 YU-NONG LI, HONG-RU LI AND LIANG-NIAN HE 5.1 INTRODUCTION 155 5.2 CO2 CONVERSION WITH C - N BOND FORMATION 157 5.2.1 SYNTHESIS OF OXAZOLIDINONES 157 5.2.1.1 OXAZOLIDINONE SYNTHESIS FROM AZIRIDINE AND CO2 158 VII 5.2.1.2 OXAZOLIDINONE SYNTHESIS FROM OLEFIN, A NITROGEN SOURCE, ANDCO2 163 5.2.1.3 5.2.1.4 OXAZOLIDINONE SYNTHESIS FROM AMINO ALCOHOLS AND CO2 164 OXAZOLIDINONE SYNTHESIS FROM CARBOXYLATIVE CYCLIZATION OF PROPARGYL AMINES WITH CO2 165 5.2.1.5 OXAZOLIDINONE SYNTHESIS FROM PROPARGYL ALCOHOL, ALIPHATIC AMINES/ 2 -AMINOETHANOLS, AND CO 2 167 5.2.1.6 PHOTOINDUCED RADICAL-INITIATED CARBOXYLATIVE CYCLIZATION OF ALLYL AMINES WITH CO2 170 5.2.2 5.2.3 5.2.4 5.3 5.3.1 5.3.1.1 5.3.1.2 SYNTHESIS OF ISOCYANATES AND LINEAR CARBAMATES 172 SYNTHESIS OF UREA DERIVATIVES 174 SYNTHESIS OF QUINAZOLINES 175 CO2 CONVERSION WITH C - O BOND FORMATION 178 SYNTHESIS OF CYCLIC CARBONATES 178 CYCLIC CARBONATE SYNTHESIS FROM EPOXIDE AND CO2 178 A-ALKYLIDENE CYCLIC CARBONATE SYNTHESIS FROM CARBOXYLATIVE CYCLIZATION OF PROPARGYL ALCOHOLS WITH CO2 181 5.3.1.3 CYCLIC CARBONATE SYNTHESIS FROM CARBOXYLATIVE CYCLIZATION OF 1,2-DIOLS WITH CO2 182 5.3.1.4 ONE-POT STEPWISE SYNTHESIS OF CYCLIC CARBONATES DIRECTLY FROM OLEFINS OR VICINAL HALOHYDRINS WITH CO2 183 5.3.2 5.4 5.4.1 5.4.2 5.4.3 5.5 SYNTHESIS OF LINEAR CARBONATES 185 CO2 CONVERSION WITH C - S BOND FORMATION 187 SYNTHESIS OF DITHIOACETALS 187 SYNTHESIS OF BENZOTHIAZOLONES 188 SYNTHESIS OF BENZOTHIAZOLES 189 CARBON-HETEROATOM BOND FORMATION FROM THE CAPTURED CO2 OR CO2 DERIVATIVES 190 5.6 CONCLUSIONS 191 ABBREVIATIONS 192 REFERENCES 193 6 CARBONYL-ENE REACTIONS OF ALKENES WITH CARBON DIOXIDE 199 YASUYUKI MORI AND MASANARI KIMURA 6.1 6.2 6.2.1 INTRODUCTION 199 CARBONYL-ENE REACTIONS OF ALKENES WITH CO2 199 ORGANOALUMINUM AND PYRIDINE DERIVATIVE-MEDIATED COUPLING REACTION 199 6.2.2 LIGHT-INDUCED COPPER-CATALYZED CARBOXYLATION OF ALLYLIC C - H BONDS 204 6.2.3 COPPER AND ALUMINUM ATE COMPOUND SYSTEM FOR CARBOXYLATION OF ALLYLIC C - H BOND OF ALKENES 208 6.2.4 COBALT-CATALYZED CARBOXYLATION OF ALLYLIC C - H BOND OF TERMINAL ALKENES 272 6.2.5 NICKEL-CATALYZED CARBONYL-ENE-TYPE REACTION OF TERMINAL ALKENES WITH CO 2 277 REFERENCES 223 VIII J 7 RECENT ADVANCES IN ELECTROCHEMICAL CARBOXYLATION OF ORGANIC COMPOUNDS FOR CO 2 VALORIZATION 225 LUCA DELL'AMICO, MARCELLA BONCHIO, AND XAVIER COMPANYO 7.1 INTRODUCTION 225 7.2 ELECTROCHEMICAL CARBOXYLATION OF UNSATURATED COMPOUNDS 228 73 ELECTROCHEMICAL CARBOXYLATION OF ORGANIC HALIDES 236 7.4 STEREOSELECTIVE ELECTROCHEMICAL CARBOXYLATIONS 245 7.5 CONCLUSIONS 249 REFERENCES 250 8 PHOTOCATALYSIS AS A POWERFUL TOOL FOR THE UTILIZATION OF CO 2 IN ORGANIC SYNTHESIS 253 DANIEL RIEMER AND SHOUBHIK DAS 8.1 KEY INTERMEDIATE INVOLVING SUBSTRATE WITH LATE-STAGE CO 2 ADDITION/ INSERTION 254 8.1.1 UNSATURATED SUBSTRATES 254 8.1.2 ARYL HALIDES 264 8.1.3 BENZYLIC C - H BONDS 267 8.2 CO 2 SUBSTRATE ADDUCT AS THE KEY INTERMEDIATE 269 8.3 CO2 RADICAL ANION AS A KEY INTERMEDIATE 276 8.4 HYDROXYCARBONYL RADICAL AS A KEY INTERMEDIATE 282 8.5 CONCLUSION AND OUTLOOK 284 REFERENCES 285 9 DIRECT CARBOXYLATION OF ALKENES AND ALKYNES 291 MARTIN PICHETTE DRAPEAU, JOHANNES SCHRANCK, AND AN IS TLILI 9.1 INTRODUCTION 291 9.2 CARBOXYLATION OF ALKENES 291 9.2.1 STOICHIOMETRIC CARBOXYLATION OF ALKENES 291 9.2.2 CATALYTIC HYDROCARBOXYLATION OF ALKENES 295 9.2.3 PHOTOINDUCED HYDROCARBOXYLATION OF ALKENES 300 9.2.4 DIFUNCTIONALIZATION OF ALKENES WITH CARBON DIOXIDE 304 9.3 CARBOXYLATION OF ALKYNES 305 9.3.1 CARBOXYLATION OF TERMINAL ALKYNES 305 9.3.1.1 SYNTHESIS OF PROPIOLIC ESTERS 305 9.3.1.2 SYNTHESIS OF PROPIOLIC ACIDS 308 9.3.2 SYNTHESIS OF ACRYLIC ACID DERIVATIVES 316 9.3.2.1 HYDROCARBOXYLATION 316 93.2.2 ALKYL AND ARYLCARBOXYLATIONS 321 93,23 SILA AND BORACARBOXYLATIONS 323 9.3.3 CARBOXYLATION LEADING TO CYCLIZATION PRODUCTS 324 9.4 CONCLUSIONS 326 REFERENCES 327 IX 10 HOMOGENEOUS IRON CATALYSTS FOR THE SYNTHESIS OF USEFUL MOLECULES FROM CO 2 331 FRANCESCO DELLA MONICA AND CARMINE CAPACCHIONE 10.1 10.2 10.2.1 10.2.2 10.2.3 10.3 10.3.1 INTRODUCTION 331 REDUCTIVE PROCESSES 332 HYDROGENATION 332 HYDROSILYLATION AND HYDROBORATION 335 MECHANISTIC DETAILS 336 NONREDUCTIVE PROCESSES 337 CYCLIC ORGANIC CARBONATES AND ALIPHATIC POLYCARBONATES FROM CO 2 AND EPOXIDES 337 10.3.2 10.3.3 10.3.4 10.4 MECHANISTIC DETAILS 346 STEREOCHEMISTRY OF CYCLIC ORGANIC CARBONATES 354 OXAZOLIDINONES 358 CONCLUSIONS 360 REFERENCES 360 11 NHC-CATALYZED CO 2 FIXATIONS IN ORGANIC SYNTHESIS 367 VLSHAKHA GOYAL, NAINA SARKI, ANAND NARANI, AND KISHORE NATTE 11.1 11.2 11.2.1 11.2.2 11.2.3 11.3 11.4 11.4.1 11.4.2 11.4.3 11.4.4 11.5 11.5.1 11.5.2 11.6 11.7 INTRODUCTION 367 DIRECT C-H ACTIVATION WITH CO 2 369 C-H ACTIVATION OF TERMINAL ALKYNES 369 CARBOXYLATION OF ARENES AND HETEROARENES 373 CARBOXYLATION OF ALKENES AND ORGANOBORONIC ESTERS 376 OXIDATION OF ALDEHYDES WITH CO 2 376 CYCLIZATION REACTIONS WITH CO 2 379 SYNTHESIS OF CYCLIC CARBONATES FROM CO 2 AND EPOXIDES 379 CYCLIZATION OF CO 2 IN PRESENCE OF NHC-CO 2 ADDUCTS 380 CYCLIZATION OF CO 2 IN PRESENCE OF METAL NHCS COMPLEXES 382 CYCLIZATION OF PROPARGYLIC AMINES 385 ALKYLATION WITH CO 2 387 N-METHYLATION 387 N-FORMYLATION 388 MISCELLANEOUS 390 SUMMARY 393 REFERENCES 393 12 SILVER-CATALYZED CO 2 FIXATION 397 KODAI SAITO AND TOHRU YAMADA 12.1 12.2 INTRODUCTION 397 HISTORICAL BACKGROUND OF CARBON DIOXIDE FIXATION INTO ORGANOSILVER COMPLEXES 398 12.3 12.4 12.5 CARBOXYLATION OF TERMINAL ALKYNES 399 CASCADE CARBOXYLATIVE CYCLIZATION 404 SILVER-CATALYZED SEQUENTIAL CARBOXYLATIVE CYCLIZATION OF PROPARGYL ALCOHOLS 405 12.6 SYNTHESIS OF CYCLIC CARBONATE 405 12.7 CATALYTIC ASYMMETRIC SYNTHESIS OF CYCLIC CARBONATE 411 12.8 THREE-COMPONENT REACTION OF PROPARGYL ALCOHOLS, CARBON DIOXIDE, AND NUCLEOPHILES 411 12.9 CCVMEDIATED TRANSFORMATION OF PROPARGYL ALCOHOLS 412 12.10 TRANSFORMATION OF AMINE DERIVATIVES 417 12.11 CASCADE CARBOXYLATION AND CYCLIZATION OF UNSATURATED AMINE DERIVATIVES 417 12.11.1 BENZOXAZINE-2-ONE FROM O-ALKYNYLANILINE AND CARBON DIOXIDE 418 12.11.2 CASCADE CARBOXYLATION - ADDITION TO ALLENES 418 12.11.3 THREE-COMPONENT REACTION OF CARBON DIOXIDE, AMINES, AND ARYLOXYALLENS 419 12.12 DOMINO CARBOXYLATION - CYCLIZATION - MIGRATION OF UNSATURATED AMINES 421 12.12.1 CARBOXYLATION INVOLVING C - C BOND FORMATION - SEQUENTIAL CYCLIZATION 423 12.12.2 CARBOXYLATION OF ENOLATE - SEQUENTIAL CYCLIZATION 423 12.12.3 CARBON DIOXIDE INCORPORATION REACTION USING OTHER CARBANIONS 427 12.13 CARBOXYLATION OF ARYLBORONIC ESTERS 428 12.13.1 FUNCTIONALIZATION OF TERMINAL EPOXIDES 431 12.14 CONCLUSION 432 REFERENCES 433 INDEX 437
any_adam_object	1
any_adam_object_boolean	1
author2	Das, Shoubhik 1980-
author2_role	edt
author2_variant	s d sd
author_GND	(DE-588)1018978429
author_facet	Das, Shoubhik 1980-
building	Verbundindex
bvnumber	BV046885778
classification_rvk	VK 5500 VK 6000
ctrlnum	(OCoLC)1289788406 (DE-599)DNB1207012084
discipline	Chemie / Pharmazie
discipline_str_mv	Chemie / Pharmazie
format	Book
fullrecord	<?xml version="1.0" encoding="UTF-8"?><collection xmlns="http://www.loc.gov/MARC21/slim"><record><leader>02491nam a2200625 c 4500</leader><controlfield tag="001">BV046885778</controlfield><controlfield tag="003">DE-604</controlfield><controlfield tag="005">20211124 </controlfield><controlfield tag="007">t</controlfield><controlfield tag="008">200907s2020 gw a\|\|\| \|\|\|\| 00\|\|\| eng d</controlfield><datafield tag="016" ind1="7" ind2=" "><subfield code="a">1207012084</subfield><subfield code="2">DE-101</subfield></datafield><datafield tag="020" ind1=" " ind2=" "><subfield code="a">9783527346134</subfield><subfield code="9">978-3-527-34613-4</subfield></datafield><datafield tag="035" ind1=" " ind2=" "><subfield code="a">(OCoLC)1289788406</subfield></datafield><datafield tag="035" ind1=" " ind2=" "><subfield code="a">(DE-599)DNB1207012084</subfield></datafield><datafield tag="040" ind1=" " ind2=" "><subfield code="a">DE-604</subfield><subfield code="b">ger</subfield><subfield code="e">rda</subfield></datafield><datafield tag="041" ind1="0" ind2=" "><subfield code="a">eng</subfield></datafield><datafield tag="044" ind1=" " ind2=" "><subfield code="a">gw</subfield><subfield code="c">XA-DE-BW</subfield></datafield><datafield tag="049" ind1=" " ind2=" "><subfield code="a">DE-11</subfield><subfield code="a">DE-29T</subfield><subfield code="a">DE-19</subfield></datafield><datafield tag="084" ind1=" " ind2=" "><subfield code="a">VK 5500</subfield><subfield code="0">(DE-625)147401:253</subfield><subfield code="2">rvk</subfield></datafield><datafield tag="084" ind1=" " ind2=" "><subfield code="a">VK 6000</subfield><subfield code="0">(DE-625)147413:253</subfield><subfield code="2">rvk</subfield></datafield><datafield tag="245" ind1="1" ind2="0"><subfield code="a">CO2 as a building block in organic synthesis</subfield><subfield code="c">edited by Shoubhik Das</subfield></datafield><datafield tag="264" ind1=" " ind2="1"><subfield code="a">Weinheim</subfield><subfield code="b">Wiley-VCH</subfield><subfield code="c">[2020]</subfield></datafield><datafield tag="264" ind1=" " ind2="4"><subfield code="c">© 2020</subfield></datafield><datafield tag="300" ind1=" " ind2=" "><subfield code="a">x, 453 Seiten</subfield><subfield code="b">Illustrationen</subfield></datafield><datafield tag="336" ind1=" " ind2=" "><subfield code="b">txt</subfield><subfield code="2">rdacontent</subfield></datafield><datafield tag="337" ind1=" " ind2=" "><subfield code="b">n</subfield><subfield code="2">rdamedia</subfield></datafield><datafield tag="338" ind1=" " ind2=" "><subfield code="b">nc</subfield><subfield code="2">rdacarrier</subfield></datafield><datafield tag="500" ind1=" " ind2=" "><subfield code="a">Die 2 im Titel ist tiefgestellt</subfield></datafield><datafield tag="650" ind1="0" ind2="7"><subfield code="a">Kohlendioxid</subfield><subfield code="0">(DE-588)4031648-8</subfield><subfield code="2">gnd</subfield><subfield code="9">rswk-swf</subfield></datafield><datafield tag="650" ind1="0" ind2="7"><subfield code="a">Carboxylierung</subfield><subfield code="0">(DE-588)4205211-7</subfield><subfield code="2">gnd</subfield><subfield code="9">rswk-swf</subfield></datafield><datafield tag="653" ind1=" " ind2=" "><subfield code="a">Anorganische Chemie</subfield></datafield><datafield tag="653" ind1=" " ind2=" "><subfield code="a">Chemie</subfield></datafield><datafield tag="653" ind1=" " ind2=" "><subfield code="a">Chemistry</subfield></datafield><datafield tag="653" ind1=" " ind2=" "><subfield code="a">CO2</subfield></datafield><datafield tag="653" ind1=" " ind2=" "><subfield code="a">Inorganic Chemistry</subfield></datafield><datafield tag="653" ind1=" " ind2=" "><subfield code="a">Kohlendioxid</subfield></datafield><datafield tag="653" ind1=" " ind2=" "><subfield code="a">Methods - Synthesis & Techniques</subfield></datafield><datafield tag="653" ind1=" " ind2=" "><subfield code="a">Organische Chemie / Methoden, Synthesen, Verfahren</subfield></datafield><datafield tag="653" ind1=" " ind2=" "><subfield code="a">Pharmaceutical & Medicinal Chemistry</subfield></datafield><datafield tag="653" ind1=" " ind2=" "><subfield code="a">Pharmazeutische u. Medizinische Chemie</subfield></datafield><datafield tag="653" ind1=" " ind2=" "><subfield code="a">CH60: Pharmazeutische u. Medizinische Chemie</subfield></datafield><datafield tag="653" ind1=" " ind2=" "><subfield code="a">CH70: Anorganische Chemie</subfield></datafield><datafield tag="653" ind1=" " ind2=" "><subfield code="a">CH81: Organische Chemie / Methoden, Synthesen, Verfahren</subfield></datafield><datafield tag="655" ind1=" " ind2="7"><subfield code="0">(DE-588)4143413-4</subfield><subfield code="a">Aufsatzsammlung</subfield><subfield code="2">gnd-content</subfield></datafield><datafield tag="689" ind1="0" ind2="0"><subfield code="a">Kohlendioxid</subfield><subfield code="0">(DE-588)4031648-8</subfield><subfield code="D">s</subfield></datafield><datafield tag="689" ind1="0" ind2="1"><subfield code="a">Carboxylierung</subfield><subfield code="0">(DE-588)4205211-7</subfield><subfield code="D">s</subfield></datafield><datafield tag="689" ind1="0" ind2=" "><subfield code="5">DE-604</subfield></datafield><datafield tag="700" ind1="1" ind2=" "><subfield code="a">Das, Shoubhik</subfield><subfield code="d">1980-</subfield><subfield code="0">(DE-588)1018978429</subfield><subfield code="4">edt</subfield></datafield><datafield tag="710" ind1="2" ind2=" "><subfield code="a">Wiley-VCH</subfield><subfield code="0">(DE-588)16179388-5</subfield><subfield code="4">pbl</subfield></datafield><datafield tag="776" ind1="0" ind2="8"><subfield code="i">Erscheint auch als</subfield><subfield code="n">Online-Ausgabe, PDF</subfield><subfield code="z">978-3-527-82194-5</subfield></datafield><datafield tag="776" ind1="0" ind2="8"><subfield code="i">Erscheint auch als</subfield><subfield code="n">Online-Ausgabe, EPUB</subfield><subfield code="z">978-3-527-82196-9</subfield></datafield><datafield tag="776" ind1="0" ind2="8"><subfield code="i">Erscheint auch als</subfield><subfield code="n">Online-Ausgabe, OBOOK</subfield><subfield code="z">978-3-527-82195-2</subfield></datafield><datafield tag="856" ind1="4" ind2="2"><subfield code="m">X:MVB</subfield><subfield code="u">http://www.wiley-vch.de/publish/dt/books/ISBN978-3-527-34613-4/</subfield></datafield><datafield tag="856" ind1="4" ind2="2"><subfield code="m">DNB Datenaustausch</subfield><subfield code="q">application/pdf</subfield><subfield code="u">http://bvbr.bib-bvb.de:8991/F?func=service&doc_library=BVB01&local_base=BVB01&doc_number=032295695&sequence=000001&line_number=0001&func_code=DB_RECORDS&service_type=MEDIA</subfield><subfield code="3">Inhaltsverzeichnis</subfield></datafield><datafield tag="999" ind1=" " ind2=" "><subfield code="a">oai:aleph.bib-bvb.de:BVB01-032295695</subfield></datafield></record></collection>
genre	(DE-588)4143413-4 Aufsatzsammlung gnd-content
genre_facet	Aufsatzsammlung
id	DE-604.BV046885778
illustrated	Illustrated
index_date	2024-07-03T15:19:30Z
indexdate	2024-07-10T08:56:33Z
institution	BVB
institution_GND	(DE-588)16179388-5
isbn	9783527346134
language	English
oai_aleph_id	oai:aleph.bib-bvb.de:BVB01-032295695
oclc_num	1289788406
open_access_boolean
owner	DE-11 DE-29T DE-19 DE-BY-UBM
owner_facet	DE-11 DE-29T DE-19 DE-BY-UBM
physical	x, 453 Seiten Illustrationen
publishDate	2020
publishDateSearch	2020
publishDateSort	2020
publisher	Wiley-VCH
record_format	marc
spelling	CO2 as a building block in organic synthesis edited by Shoubhik Das Weinheim Wiley-VCH [2020] © 2020 x, 453 Seiten Illustrationen txt rdacontent n rdamedia nc rdacarrier Die 2 im Titel ist tiefgestellt Kohlendioxid (DE-588)4031648-8 gnd rswk-swf Carboxylierung (DE-588)4205211-7 gnd rswk-swf Anorganische Chemie Chemie Chemistry CO2 Inorganic Chemistry Kohlendioxid Methods - Synthesis & Techniques Organische Chemie / Methoden, Synthesen, Verfahren Pharmaceutical & Medicinal Chemistry Pharmazeutische u. Medizinische Chemie CH60: Pharmazeutische u. Medizinische Chemie CH70: Anorganische Chemie CH81: Organische Chemie / Methoden, Synthesen, Verfahren (DE-588)4143413-4 Aufsatzsammlung gnd-content Kohlendioxid (DE-588)4031648-8 s Carboxylierung (DE-588)4205211-7 s DE-604 Das, Shoubhik 1980- (DE-588)1018978429 edt Wiley-VCH (DE-588)16179388-5 pbl Erscheint auch als Online-Ausgabe, PDF 978-3-527-82194-5 Erscheint auch als Online-Ausgabe, EPUB 978-3-527-82196-9 Erscheint auch als Online-Ausgabe, OBOOK 978-3-527-82195-2 X:MVB http://www.wiley-vch.de/publish/dt/books/ISBN978-3-527-34613-4/ DNB Datenaustausch application/pdf http://bvbr.bib-bvb.de:8991/F?func=service&doc_library=BVB01&local_base=BVB01&doc_number=032295695&sequence=000001&line_number=0001&func_code=DB_RECORDS&service_type=MEDIA Inhaltsverzeichnis
spellingShingle	CO2 as a building block in organic synthesis Kohlendioxid (DE-588)4031648-8 gnd Carboxylierung (DE-588)4205211-7 gnd
subject_GND	(DE-588)4031648-8 (DE-588)4205211-7 (DE-588)4143413-4
title	CO2 as a building block in organic synthesis
title_auth	CO2 as a building block in organic synthesis
title_exact_search	CO2 as a building block in organic synthesis
title_exact_search_txtP	CO2 as a building block in organic synthesis
title_full	CO2 as a building block in organic synthesis edited by Shoubhik Das
title_fullStr	CO2 as a building block in organic synthesis edited by Shoubhik Das
title_full_unstemmed	CO2 as a building block in organic synthesis edited by Shoubhik Das
title_short	CO2 as a building block in organic synthesis
title_sort	co2 as a building block in organic synthesis
topic	Kohlendioxid (DE-588)4031648-8 gnd Carboxylierung (DE-588)4205211-7 gnd
topic_facet	Kohlendioxid Carboxylierung Aufsatzsammlung
url	http://www.wiley-vch.de/publish/dt/books/ISBN978-3-527-34613-4/ http://bvbr.bib-bvb.de:8991/F?func=service&doc_library=BVB01&local_base=BVB01&doc_number=032295695&sequence=000001&line_number=0001&func_code=DB_RECORDS&service_type=MEDIA
work_keys_str_mv	AT dasshoubhik co2asabuildingblockinorganicsynthesis AT wileyvch co2asabuildingblockinorganicsynthesis

Verfügbarkeit

Es ist kein Print-Exemplar vorhanden.

Fernleihe Bestellen Achtung: Nicht im THWS-Bestand! Inhaltsverzeichnis

MARC

Datensatz im Suchindex

Es ist kein Print-Exemplar vorhanden.

Ähnliche Einträge