Multicomponent reactions in organic synthesis:
Gespeichert in:
| Weitere Verfasser: | |
|---|---|
| Format: | Buch |
| Sprache: | English |
| Veröffentlicht: |
Weinheim
WILEY-VCH
2015
|
| Schlagworte: | |
| Online-Zugang: | Inhaltsverzeichnis |
| Beschreibung: | XVIII, 493 S. Ill., graph. Darst. |
| ISBN: | 9783527332373 9783527678174 |
Internformat
MARC
| LEADER | 00000nam a2200000 c 4500 | ||
|---|---|---|---|
| 001 | BV042259293 | ||
| 003 | DE-604 | ||
| 005 | 20150827 | ||
| 007 | t | ||
| 008 | 150108s2015 gw ad|| |||| 00||| eng d | ||
| 020 | |a 9783527332373 |9 978-3-527-33237-3 | ||
| 020 | |a 9783527678174 |c oBook |9 978-3-527-67817-4 | ||
| 035 | |a (OCoLC)904468593 | ||
| 035 | |a (DE-599)BVBBV042259293 | ||
| 040 | |a DE-604 |b ger |e rakwb | ||
| 041 | 0 | |a eng | |
| 044 | |a gw |c XA-DE-BW | ||
| 049 | |a DE-11 |a DE-20 |a DE-19 | ||
| 050 | 0 | |a QD501 | |
| 082 | 0 | |a 547.2 | |
| 084 | |a VK 5500 |0 (DE-625)147401:253 |2 rvk | ||
| 084 | |a VK 6000 |0 (DE-625)147413:253 |2 rvk | ||
| 084 | |a CHE 620f |2 stub | ||
| 084 | |a 540 |2 sdnb | ||
| 245 | 1 | 0 | |a Multicomponent reactions in organic synthesis |c ed. by Jieping Zhu ... |
| 264 | 1 | |a Weinheim |b WILEY-VCH |c 2015 | |
| 300 | |a XVIII, 493 S. |b Ill., graph. Darst. | ||
| 336 | |b txt |2 rdacontent | ||
| 337 | |b n |2 rdamedia | ||
| 338 | |b nc |2 rdacarrier | ||
| 650 | 4 | |a Eintopfreaktion | |
| 650 | 4 | |a Catalyse | |
| 650 | 4 | |a Catalysis | |
| 650 | 4 | |a Chemical reactions | |
| 650 | 4 | |a Chemistry, Organic | |
| 650 | 4 | |a Chimie organique | |
| 650 | 4 | |a Réactions organiques (Chimie) | |
| 650 | 0 | 7 | |a Organische Synthese |0 (DE-588)4075695-6 |2 gnd |9 rswk-swf |
| 650 | 0 | 7 | |a Eintopfreaktion |0 (DE-588)4254931-0 |2 gnd |9 rswk-swf |
| 655 | 7 | |0 (DE-588)4143413-4 |a Aufsatzsammlung |2 gnd-content | |
| 689 | 0 | 0 | |a Eintopfreaktion |0 (DE-588)4254931-0 |D s |
| 689 | 0 | 1 | |a Organische Synthese |0 (DE-588)4075695-6 |D s |
| 689 | 0 | |5 DE-604 | |
| 700 | 1 | |a Zhu, Jieping |0 (DE-588)1064679536 |4 edt | |
| 776 | 0 | 8 | |i Erscheint auch als |n Online-Ausgabe, EPUB |z 978-3-527-67820-4 |
| 776 | 0 | 8 | |i Erscheint auch als |n Online-Ausgabe, MOBI |z 978-3-527-67818-1 |
| 776 | 0 | 8 | |i Erscheint auch als |n Online-Ausgabe, PDF |z 978-3-527-67819-8 |
| 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=027697109&sequence=000001&line_number=0001&func_code=DB_RECORDS&service_type=MEDIA |3 Inhaltsverzeichnis |
| 999 | |a oai:aleph.bib-bvb.de:BVB01-027697109 | ||
Datensatz im Suchindex
| _version_ | 1804152810995974144 |
|---|---|
| adam_text | CONTENTS
LIST OF CONTRIBUTORS
XIII
PREFACE
XVII
1 GENERAL INTRODUCTION TO MCRS:
PAST, PRESENT, AND FUTURE 1
ALEXANDER DOMLING AND ALANOD D. AIQAHTANI
1.1 INTRODUCTION 1
1.2 ADVANCES IN CHEMISTRY 2
1.3 TOTAL SYNTHESES 4
1.4 APPLICATIONS IN PHARMACEUTICAL AND AGROCHEMICAL
INDUSTRY 4
1.5 MATERIALS 10
1.6 OUTLOOK 10
REFERENCES 11
2 DISCOVERY OF MCRS 13
EELCO RUIJTER AND ROMANO V.A. ORRU
2.1 GENERAL INTRODUCTION
13
2.2 THE CONCEPT 14
2.3 THE REACTION DESIGN CONCEPT 15
2.3.1 SINGLE REACTANT REPLACEMENT 17
2.3.2 MODULAR REACTION SEQUENCES 19
2.3.3 CONDITION-BASED DIVERGENCE 21
2.3.4 UNION OF MCRS 23
2.4 MULTICOMPONENT REACTIONS AND BIOCATALYSIS 23
2.4.1 MULTICOMPONENT REACTIONS AND (DYNAMIC) ENZYMATIC
KINETIC RESOLUTION 26
2.4.2 MULTICOMPONENT REACTIONS AND ENZYMATIC DESYMMETRIZATION 29
2.5 MULTICOMPONENT REACTIONS IN GREEN PHARMACEUTICAL
PRODUCTION 31
2.6 CONCLUSIONS 36
ACKNOWLEDGMENTS 36
REFERENCES 36
HTTP://D-NB.INFO/1052323669
VI |
CONTENTS
3 ARYNE-BASED MULTICOMPONENT REACTIONS 39
HIROTO YOSHIDA
3.1 INTRODUCTION 39
3.2 MULTICOMPONENT REACTIONS OF ARYNES VIA ELECTROPHILIC
COUPLING 41
3.2.1 MULTICOMPONENT REACTIONS UNDER NEUTRAL CONDITIONS 42
3.2.1.1 ISOCYANIDE-BASED MULTICOMPONENT REACTIONS 42
3.2.1.2 IMINE-BASED MULTICOMPONENT REACTIONS 46
3.2.1.3 AMINE-BASED MULTICOMPONENT REACTIONS 47
3.2.1.4 CARBONYL COMPOUND-BASED MULTICOMPONENT REACTIONS 49
3.2.1.5 ETHER-BASED MULTICOMPONENT REACTIONS 50
3.2.1.6 MISCELLANEOUS 53
3.2.2 MULTICOMPONENT REACTIONS UNDER BASIC CONDITIONS 53
3.3 TRANSITION METAL-CATALYZED MULTICOMPONENT REACTIONS OF ARYNES 60
3.3.1 ANNULATIONS 60
3.3.2 CROSS-COUPLING-TYPE REACTIONS 65
3.3.3 MIZOROKI-HECK-TYPE REACTIONS 65
3.3.4 INSERTION INTO O-BOND 65
3.4 CONCLUDING REMARKS 69
REFERENCES 69
4 UGI-SMILES AND PASSERINI-SMILES COUPLINGS 73
LAURENT EL KA IM AND LAURENCE GRIMAUD
4.1 INTRODUCTION 73
4.1.1 CARBOXYLIC ACID SURROGATES IN UGI REACTIONS 75
4.1.2 SMILES REARRANGEMENTS 76
4.2 SCOPE AND LIMITATIONS 77
4.2.1 PHENOLS AND THIOPHENOLS 77
4.2.2 SIX-MEMBERED RING HYDROXY HETEROAROMATICS AND RELATED
MERCAPTANS 84
4.2.3 FIVE-MEMBERED RING HYDROXY HETEROAROMATIC AND RELATED
MERCAPTANS
88
4.2.4 RELATED COUPLINGS WITH ENOL DERIVATIVES 90
4.2.5 THE JOULLIE-SMILES COUPLING 90
4.2.6 THE PASSERINI-SMILES REACTION 91
4.3 UGI-SMILES POSTCONDENSATIONS 94
4.3.1 POSTCONDENSATIONS INVOLVING REDUCTION OF THE NITRO GROUP 94
4.3.2 TRANSFORMATIONS OF UGI-SMILES THIOAMIDES 96
4.3.3 POSTCONDENSATIONS INVOLVING TRANSITION METAL-CATALYZED
PROCESSES 97
4.3.4 REACTIVITY OF THE PEPTIDYL UNIT 101
4.3.5 RADICAL REACTIONS 103
4.3.6 CYCLOADDITION 103
4.4 CONCLUSIONS 105
REFERENCES 105
CONTENTS
IVII
5 1,3-DICARBONYLS IN MULTICOMPORIENT REACTIONS 109
XAVIER BUGAUT, THIERRY CONSTANTIEUX, YOANN COQUEREL, AND JEAN RODRIGUEZ
5.1 INTRODUCTION 109
5.2 ACHIRAL AND RACEMIC MCRS 111
5.2.1 INVOLVING ONE PRONUCLEOPHILIC REACTIVE SITE 111
5.2.2 INVOLVING TWO REACTIVE SITES 115
5.2.2.1 TWO NUCLEOPHILIC SITES 115
5.2.2.2 ONE PRONUCLEOPHILIC SITE AND ONE ELECTROPHILIC SITE 120
5.2.3 INVOLVING THREE REACTIVE SITES 134
5.2.4 INVOLVING FOUR REACTIVE SITES 139
5.3 ENANTIOSELECTIVE MCRS 142
5.3.1 INVOLVING ONE REACTIVE SITE 143
5.3.2 INVOLVING TWO REACTIVE SITES 146
5.3.3 INVOLVING THREE REACTIVE SITES 149
5.4 CONCLUSIONS AND OUTLOOK 150
REFERENCES 151
6 FUNCTIONALIZATION OF HETEROCYDES BY MCRS 159
ESTHER VICENTE-GARCIA, NICOLA KIELLAND, AND RODOLFO LAVILLA
6.1 INTRODUCTION 159
6.2 MANNICH-TYPE REACTIONS AND RELATED PROCESSES 160
6.3 P-DICARBONYL CHEMISTRY 164
6.4 HETERO-DIELS-ALDER CYCLOADDITIONS AND RELATED PROCESSES 166
6.5 METAL-MEDIATED PROCESSES 168
6.6 ISOCYANIDE-BASED REACTIONS 171
6.7 DIPOLE-MEDIATED PROCESSES 175
6.8 CONCLUSIONS 176
ACKNOWLEDGMENTS 178
REFERENCES 178
7 OIAZOACETATE AND RELATED METAL-STABILIZED CARBENE
SPECIES IN MCRS 183
DONG XING AND WENHAO HU
7.1 INTRODUCTION 183
1.2 MCRS VIA CARBONYL OR AZOMETHINE YLIDE-INVOLVED
1,3-DIPOLAR CYCLOADDITIONS 184
7.2.1 AZOMETHINE YLIDE 184
7.2.2 CARBONYL YLIDE 185
7.3 MCRS VIA ELECTROPHILIC TRAPPING OF PROTIC ONIUM YLIDES 187
7.3.1 INITIAL DEVELOPMENT 187
7.3.2 ASYMMETRIC EXAMPLES 190
7.3.2.1 CHIRAL REAGENT INDUCTION 190
7.3.2.2 CHIRAL DIRHODIUM(II) CATALYSIS 190
7.3.2.3 ENANTIOSELECTIVE SYNERGISTIC CATALYSIS 190
7.3.3 MCRS FOLLOWED BY TANDEM CYCLIZATIONS 196
VIII
|
CONTENTS
7.4 MCRS VIA ELECTROPHILIC TRAPPING OF ZWITTERIONIC INTERMEDIATES 198
7.5 MCRS VIA METAL CARBENE MIGRATORY INSERTION 199
7.6 SUMMARY AND OUTLOOK 203
REFERENCES 204
8 METAL-CATALYZED MULTICOMPONENT SYNTHESIS OF HETEROCYDES 207
FABIO LORENZINI, JEVGENIJS TJUTRINS, JEFFREY S. QUESNEL, AND BRUCE A.
ARNDTSEN
8.1 INTRODUCTION 207
8.2 MULTICOMPONENT CROSS-COUPLING AND CARBONYLATION REACTIONS 208
8.2.1 CYCLIZATION WITH ALKYNE- OR ALKENE-CONTAINING NUCLEOPHILES 208
8.2.2 CYCLIZATION VIA PALLADIUM-ALLYL COMPLEXES 210
8.2.3 FUSED-RING HETEROCYCLES FOR ORFAO-SUBSTITUTED ARENE BUILDING
BLOCKS 211
8.2.4 MULTICOMPONENT CYCLOCARBONYLATIONS 214
8.2.5 CYCLIZATION OF CROSS-COUPLING REACTION PRODUCTS 216
8.2.6 C-H FUNCTIONALIZATION IN MULTICOMPONENT REACTIONS 218
8.3 METALLACYCLES IN MULTICOMPONENT REACTIONS 22J
8.4 MULTICOMPONENT REACTIONS VIA 1,3-DIPOLAR CYCLOADDITION 223
8.5 CONCLUDING REMARKS 227
REFERENCES 227
9 MACROCYDES FROM MULTICOMPONENT REACTIONS 231
LUDGER
A
WESSJOHANN, RICARDO A.W. NEVES FILHO, ALFREDO
R. PUENTES, AND
MICJEL C. MOREJON
9.1 INTRODUCTION 231
9.2 IMCR-BASED MACROCYCLIZATIONS OF SINGLE BIFUNCTIONAL BUILDING
BLOCKS 237
9.3 MULTIPLE MCR-BASED MACROCYCLIZATIONS OF BIFUNCTIONAL BUILDING
BLOCKS 245
9.4 IMCR-BASED MACROCYCLIZATIONS OF TRIFUNCTIONALIZED BUILDING
BLOCKS (MIB-3D) 256
9.5 SEQUENTIAL IMCR-BASED MACROCYCLIZATIONS OF MULTIPLE BIFUNCTIONAL
BUILDING BLOCKS 259
9.6 FINAL REMARKS AND FUTURE PERSPECTIVES 261
REFERENCES 261
10 MULTICOMPONENT REACTIONS UNDER OXIDATIVE CONDITIONS 265
ANDREA BASSO, LISA MONI, AND RENATA RIVA
10.1 INTRODUCTION 265
10.2 MULTICOMPONENT REACTIONS INVOLVING IN SITU OXIDATION OF ONE
SUBSTRATE 266
10.2.1 ISOCYANIDE-BASED MULTICOMPONENT REACTIONS 266
10.2.1.1 PASSERINI REACTIONS 266
10.2.1.2 UGI REACTIONS WITH IN SITU OXIDATION OF ALCOHOLS 271
10.2.1.3 UGI REACTION WITH IN SITU OXIDATION OF SECONDARY AMINES 273
CONTENTS
J IX
10.2.1.4 UGI-SMILES REACTION WITH IN SITU OXIDATION OF SECONDARY
AMINES 275
10.2.1.5 UGI-TYPE REACTIONS BY IN SITU OXIDATION OF TERTIARY AMINES 277
10.2.1.6 SYNTHESIS OF OTHER DERIVATIVES 279
10.2.2 OTHER MULTICOMPONENT REACTIONS 280
10.3 MULTICOMPONENT REACTIONS INVOLVING OXIDATION OF A REACTION
INTERMEDIATE 284
10.3.1 REACTIONS WITHOUT TRANSITION METAL-MEDIATED OXIDATION 285
10.3.2 REACTIONS MEDIATED BY TRANSITION METAL CATALYSIS 292
10.4 MULTICOMPONENT REACTIONS INVOLVING OXIDANTS AS LEWIS ACIDS 295
10.5 CONCLUSIONS 297
REFERENCES 297
11 ALLENES IN MULTICOMPONENT SYNTHESIS OF HETEROCYCFES 301
HANS-ULRICH REISSIG
AND REINHOLD ZIMMER
11.1 INTRODUCTION 301
11.2 REACTIONS WITH 1,2-PROPADIENE AND UNACTIVATED ALLENES 302
11.2.1 PALLADIUM-CATALYZED MULTICOMPONENT REACTIONS 302
11.2.2 COPPER-, NICKEL-, AND RHODIUM-PROMOTED MULTICOMPONENT
REACTIONS 310
11.2.3 MULTICOMPONENT REACTIONS WITHOUT TRANSITION METALS 314
11.3 REACTIONS WITH ACCEPTOR-SUBSTITUTED ALLENES 316
11.3.1 CATALYZED MULTICOMPONENT REACTIONS 316
11.3.2 UNCATALYZED MULTICOMPONENT REACTIONS 318
11.4 REACTIONS WITH DONOR-SUBSTITUTED ALLENES 323
11.5 CONCLUSIONS 329
LIST OF ABBREVIATIONS 329
REFERENCES 329
12 ALKYNES IN MULTICOMPONENT SYNTHESIS OF HETEROEYDES 333
THOMAS J J. MULLER AND KONSTANTIN DEILHOF
12.1 INTRODUCTION 333
12.2 O-NUCLEOPHILIC REACTIVITY OF ALKYNES 335
12.2.1 ACETYLIDE ADDITIONS TO ELECTROPHILES 335
12.2.1.1 ALKYNE-ALDEHYDE-AMINE CONDENSATION - A
3
-COUPLING 335
12.2.1.2 ALKYNE-(HETERO)ARYL HALIDE (SONOGASHIRA) COUPLING AS KEY
REACTION 337
12.2.2 CONVERSION OF TERMINAL ALKYNES INTO ELECTROPHILES AS
KEY REACTIONS 341
12.3 JC-NUCLEOPHILIC REACTIVITY OF ALKYNES 345
12.4 ALKYNES AS ELECTROPHILIC PARTNERS 351
12.5 ALKYNES IN CYCLOADDITIONS 356
12.5.1 ALKYNES AS DIPOLAROPHILES 356
12.5.2 ALKYNES IN CU(I)-CATALYZED 1,3-DIPOLAR AZIDE-ALKYNE
CYCLOADDITION 358
X|
CONTENTS
12.5.3 ALKYNES AS DIENOPHILES IN MCRS 366
12.6 ALKYNES AS REACTION PARTNERS IN ORGANOMETALLIC MCRS 370
12.7 CONCLUSIONS 374
LIST OF ABBREVIATIONS 374
ACKNOWLEDGMENT 375
REFERENCES 375
13 ANHYDRIDE-BASED MULTICOMPONENT REACTIONS 379
KEVIN S. MARTIN, JARED T. SHAW, AND ASHKAAN YOUNAI
13.1 INTRODUCTION 379
13.2 QUINOLONES AND RELATED HETEROCYCLES FROM HOMOPHTHALIC
AND ISATOIC ANHYDRIDES 380
13.2.1 INTRODUCTION: REACTIVITY OF HOMOPHTHALIC AND ISATOIC
ANHYDRIDES 380
13.2.2 IMINE-ANHYDRIDE REACTIONS OF HOMOPHTHALIC ANHYDRIDE 380
13.2.3 MCRS EMPLOYING HOMOPHTHALIC ANHYDRIDE 382
13.2.4 IMINE-ANHYDRIDE REACTIONS OF ISATOIC ANHYDRIDE 383
13.3 A,P-UNSATURATED CYCLIC ANHYDRIDES: MCRS INVOLVING CONJUGATE
ADDITION AND CYCLOADDITION REACTIONS 385
13.3.1 MALEIC ANHYDRIDE MCRS 385
13.3.2 MCRS OF ITACONIC ANHYDRIDES 388
13.3.3 DIELS-ALDER REACTIONS 390
13.4 MCRS OF CYCLIC ANHYDRIDES IN ANNULATION REACTIONS AND
RELATED PROCESSES 392
13.4.1 MCR-BASED ANNULATIONS: SUCCINIC AND PHTHALIC ANHYDRIDES 393
13.5 MCRS OF ACYCLIC ANHYDRIDES 395
13.6 CONCLUSIONS 398
REFERENCES 399
14 FREE-RADICAL MULTICOMPONENT
PROCESSES 401
VIRGINIE LIAUTARD AND YANNICK LANDAIS
14.1 INTRODUCTION 401
14.2 MCRS INVOLVING ADDITION ACROSS OLEFIN C=C BONDS 402
14.2.1 ADDITION OF ARYL RADICALS TO OLEFINS 402
14.2.2 MCRS USING SULFONYL DERIVATIVES AS TERMINAL TRAP 404
14.2.3 CARBOALLYLATION OF ELECTRON-POOR OLEFINS 406
14.2.4 CARBOHYDROXYLATION, SULFENYLATION, AND PHOSPHORYLATION
OF OLEFINS 407
14.2.5 RADICAL ADDITION TO OLEFINS USING PHOTOREDOX CATALYSIS 410
14.2.6 MCRS BASED ON RADICAL-POLAR CROSSOVER PROCESSES 414
14.3 FREE-RADICAL CARBONYLATION 419
14.3.1 ALKYL HALIDE CARBONYLATION 419
14.3.2 METAL-MEDIATED ATOM-TRANSFER RADICAL CARBONYLATION 420
14.3.3 ALKANE CARBONYLATION 421
14.3.4 MISCELLANEOUS CARBONYLATION REACTIONS 423
CONTENTS
IXI
14.4 FREE-RADICAL OXYGENATION 424
14.5 MCRS INVOLVING ADDITION ACROSS JT-C=N BONDS 427
14.5.1 FREE-RADICAL STRECKER PROCESS 427
14.5.2 FREE-RADICAL MANNICH-TYPE PROCESSES 429
14.6 MISCELLANEOUS FREE-RADICAL MULTICOMPONENT REACTIONS 432
14.7 CONCLUSIONS 434
REFERENCES 435
15 CHIRAL PHOSPHORIC ACID-CATALYZED
ASYMMETRIC MULTICOMPONENT
REACTIONS 439
XIANG WU AND LIU-ZHU GONG
15.1 INTRODUCTION 439
15.2 MANNICH REACTION 439
15.3 UGI-TYPE REACTION 442
15.4 BIGINELLI REACTION 444
15.5 AZA-DIELS-AJDER REACTION 446
15.6 1,3-DIPOLAR CYCLOADDITION 454
15.7 HANTZSCH DIHYDROPYRIDINE SYNTHESIS 458
15.8 THE COMBINATION OF METAL AND CHIRAL PHOSPHORIC ACID
FOR MULTICOMPONENT REACTION 459
15.9 OTHER PHOSPHORIC ACID-CATALYZED MULTICOMPONENT REACTIONS 465
15.10 SUMMARY 467
REFERENCES 467
INDEX 471
|
| any_adam_object | 1 |
| author2 | Zhu, Jieping |
| author2_role | edt |
| author2_variant | j z jz |
| author_GND | (DE-588)1064679536 |
| author_facet | Zhu, Jieping |
| building | Verbundindex |
| bvnumber | BV042259293 |
| callnumber-first | Q - Science |
| callnumber-label | QD501 |
| callnumber-raw | QD501 |
| callnumber-search | QD501 |
| callnumber-sort | QD 3501 |
| callnumber-subject | QD - Chemistry |
| classification_rvk | VK 5500 VK 6000 |
| classification_tum | CHE 620f |
| ctrlnum | (OCoLC)904468593 (DE-599)BVBBV042259293 |
| dewey-full | 547.2 |
| dewey-hundreds | 500 - Natural sciences and mathematics |
| dewey-ones | 547 - Organic chemistry |
| dewey-raw | 547.2 |
| dewey-search | 547.2 |
| dewey-sort | 3547.2 |
| dewey-tens | 540 - Chemistry and allied sciences |
| discipline | Chemie / Pharmazie Chemie |
| format | Book |
| fullrecord | <?xml version="1.0" encoding="UTF-8"?><collection xmlns="http://www.loc.gov/MARC21/slim"><record><leader>02078nam a2200553 c 4500</leader><controlfield tag="001">BV042259293</controlfield><controlfield tag="003">DE-604</controlfield><controlfield tag="005">20150827 </controlfield><controlfield tag="007">t</controlfield><controlfield tag="008">150108s2015 gw ad|| |||| 00||| eng d</controlfield><datafield tag="020" ind1=" " ind2=" "><subfield code="a">9783527332373</subfield><subfield code="9">978-3-527-33237-3</subfield></datafield><datafield tag="020" ind1=" " ind2=" "><subfield code="a">9783527678174</subfield><subfield code="c">oBook</subfield><subfield code="9">978-3-527-67817-4</subfield></datafield><datafield tag="035" ind1=" " ind2=" "><subfield code="a">(OCoLC)904468593</subfield></datafield><datafield tag="035" ind1=" " ind2=" "><subfield code="a">(DE-599)BVBBV042259293</subfield></datafield><datafield tag="040" ind1=" " ind2=" "><subfield code="a">DE-604</subfield><subfield code="b">ger</subfield><subfield code="e">rakwb</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-20</subfield><subfield code="a">DE-19</subfield></datafield><datafield tag="050" ind1=" " ind2="0"><subfield code="a">QD501</subfield></datafield><datafield tag="082" ind1="0" ind2=" "><subfield code="a">547.2</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="084" ind1=" " ind2=" "><subfield code="a">CHE 620f</subfield><subfield code="2">stub</subfield></datafield><datafield tag="084" ind1=" " ind2=" "><subfield code="a">540</subfield><subfield code="2">sdnb</subfield></datafield><datafield tag="245" ind1="1" ind2="0"><subfield code="a">Multicomponent reactions in organic synthesis</subfield><subfield code="c">ed. by Jieping Zhu ...</subfield></datafield><datafield tag="264" ind1=" " ind2="1"><subfield code="a">Weinheim</subfield><subfield code="b">WILEY-VCH</subfield><subfield code="c">2015</subfield></datafield><datafield tag="300" ind1=" " ind2=" "><subfield code="a">XVIII, 493 S.</subfield><subfield code="b">Ill., graph. Darst.</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="650" ind1=" " ind2="4"><subfield code="a">Eintopfreaktion</subfield></datafield><datafield tag="650" ind1=" " ind2="4"><subfield code="a">Catalyse</subfield></datafield><datafield tag="650" ind1=" " ind2="4"><subfield code="a">Catalysis</subfield></datafield><datafield tag="650" ind1=" " ind2="4"><subfield code="a">Chemical reactions</subfield></datafield><datafield tag="650" ind1=" " ind2="4"><subfield code="a">Chemistry, Organic</subfield></datafield><datafield tag="650" ind1=" " ind2="4"><subfield code="a">Chimie organique</subfield></datafield><datafield tag="650" ind1=" " ind2="4"><subfield code="a">Réactions organiques (Chimie)</subfield></datafield><datafield tag="650" ind1="0" ind2="7"><subfield code="a">Organische Synthese</subfield><subfield code="0">(DE-588)4075695-6</subfield><subfield code="2">gnd</subfield><subfield code="9">rswk-swf</subfield></datafield><datafield tag="650" ind1="0" ind2="7"><subfield code="a">Eintopfreaktion</subfield><subfield code="0">(DE-588)4254931-0</subfield><subfield code="2">gnd</subfield><subfield code="9">rswk-swf</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">Eintopfreaktion</subfield><subfield code="0">(DE-588)4254931-0</subfield><subfield code="D">s</subfield></datafield><datafield tag="689" ind1="0" ind2="1"><subfield code="a">Organische Synthese</subfield><subfield code="0">(DE-588)4075695-6</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">Zhu, Jieping</subfield><subfield code="0">(DE-588)1064679536</subfield><subfield code="4">edt</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">978-3-527-67820-4</subfield></datafield><datafield tag="776" ind1="0" ind2="8"><subfield code="i">Erscheint auch als</subfield><subfield code="n">Online-Ausgabe, MOBI</subfield><subfield code="z">978-3-527-67818-1</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">978-3-527-67819-8</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=027697109&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:BVB01-027697109</subfield></datafield></record></collection> |
| genre | (DE-588)4143413-4 Aufsatzsammlung gnd-content |
| genre_facet | Aufsatzsammlung |
| id | DE-604.BV042259293 |
| illustrated | Illustrated |
| indexdate | 2024-07-10T01:16:38Z |
| institution | BVB |
| isbn | 9783527332373 9783527678174 |
| language | English |
| oai_aleph_id | oai:aleph.bib-bvb.de:BVB01-027697109 |
| oclc_num | 904468593 |
| open_access_boolean | |
| owner | DE-11 DE-20 DE-19 DE-BY-UBM |
| owner_facet | DE-11 DE-20 DE-19 DE-BY-UBM |
| physical | XVIII, 493 S. Ill., graph. Darst. |
| publishDate | 2015 |
| publishDateSearch | 2015 |
| publishDateSort | 2015 |
| publisher | WILEY-VCH |
| record_format | marc |
| spelling | Multicomponent reactions in organic synthesis ed. by Jieping Zhu ... Weinheim WILEY-VCH 2015 XVIII, 493 S. Ill., graph. Darst. txt rdacontent n rdamedia nc rdacarrier Eintopfreaktion Catalyse Catalysis Chemical reactions Chemistry, Organic Chimie organique Réactions organiques (Chimie) Organische Synthese (DE-588)4075695-6 gnd rswk-swf Eintopfreaktion (DE-588)4254931-0 gnd rswk-swf (DE-588)4143413-4 Aufsatzsammlung gnd-content Eintopfreaktion (DE-588)4254931-0 s Organische Synthese (DE-588)4075695-6 s DE-604 Zhu, Jieping (DE-588)1064679536 edt Erscheint auch als Online-Ausgabe, EPUB 978-3-527-67820-4 Erscheint auch als Online-Ausgabe, MOBI 978-3-527-67818-1 Erscheint auch als Online-Ausgabe, PDF 978-3-527-67819-8 DNB Datenaustausch application/pdf http://bvbr.bib-bvb.de:8991/F?func=service&doc_library=BVB01&local_base=BVB01&doc_number=027697109&sequence=000001&line_number=0001&func_code=DB_RECORDS&service_type=MEDIA Inhaltsverzeichnis |
| spellingShingle | Multicomponent reactions in organic synthesis Eintopfreaktion Catalyse Catalysis Chemical reactions Chemistry, Organic Chimie organique Réactions organiques (Chimie) Organische Synthese (DE-588)4075695-6 gnd Eintopfreaktion (DE-588)4254931-0 gnd |
| subject_GND | (DE-588)4075695-6 (DE-588)4254931-0 (DE-588)4143413-4 |
| title | Multicomponent reactions in organic synthesis |
| title_auth | Multicomponent reactions in organic synthesis |
| title_exact_search | Multicomponent reactions in organic synthesis |
| title_full | Multicomponent reactions in organic synthesis ed. by Jieping Zhu ... |
| title_fullStr | Multicomponent reactions in organic synthesis ed. by Jieping Zhu ... |
| title_full_unstemmed | Multicomponent reactions in organic synthesis ed. by Jieping Zhu ... |
| title_short | Multicomponent reactions in organic synthesis |
| title_sort | multicomponent reactions in organic synthesis |
| topic | Eintopfreaktion Catalyse Catalysis Chemical reactions Chemistry, Organic Chimie organique Réactions organiques (Chimie) Organische Synthese (DE-588)4075695-6 gnd Eintopfreaktion (DE-588)4254931-0 gnd |
| topic_facet | Eintopfreaktion Catalyse Catalysis Chemical reactions Chemistry, Organic Chimie organique Réactions organiques (Chimie) Organische Synthese Aufsatzsammlung |
| url | http://bvbr.bib-bvb.de:8991/F?func=service&doc_library=BVB01&local_base=BVB01&doc_number=027697109&sequence=000001&line_number=0001&func_code=DB_RECORDS&service_type=MEDIA |
| work_keys_str_mv | AT zhujieping multicomponentreactionsinorganicsynthesis |