Metal-catalyzed reactions in water:
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| Format: | Buch |
| Sprache: | English |
| Veröffentlicht: |
Weinheim
Wiley-VCH-Verl.
2013
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| Schriftenreihe: | Green chemistry
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| Schlagworte: | |
| Online-Zugang: | Inhaltstext Inhaltsverzeichnis |
| Beschreibung: | Literaturangaben |
| Beschreibung: | XVII, 407 S. Ill., graph. Darst. 25 cm |
| ISBN: | 3527331883 9783527331888 9783527656790 |
Internformat
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| 020 | |a 9783527656790 |c oBook |9 978-3-527-65679-0 | ||
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| 245 | 1 | 0 | |a Metal-catalyzed reactions in water |c ed. by Pierre H. Dixneuf ... |
| 264 | 1 | |a Weinheim |b Wiley-VCH-Verl. |c 2013 | |
| 300 | |a XVII, 407 S. |b Ill., graph. Darst. |c 25 cm | ||
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| 337 | |b n |2 rdamedia | ||
| 338 | |b nc |2 rdacarrier | ||
| 490 | 0 | |a Green chemistry | |
| 500 | |a Literaturangaben | ||
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Datensatz im Suchindex
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IMAGE 1
CONTENTS
PREFACE XIII
LIST O F CONTRIBUTORS X V
1 METAL-CATALYZED CROSS-COUPLINGS O F ARYL HALIDES TO FORM C-C BONDS IN
AQUEOUS MEDIA 1 KEVIN H. SHAUGHNESSY
1.1 INTRODUCTION 1
1.2 AQUEOUS-PHASE CROSS-COUPLING USING HYDROPHILIC CATALYSTS 3 1.2.1
HYDROPHILIC TRIARYLPHOSPHINES A N D DIARYLALKYLPHOSPINES 3 1.2.2
STERICALLY DEMANDING, HYDROPHILIC TRIALKYL A N D DIALKYLBIARYLPHOSPHINES
7
1.2.3 N H C LIGANDS 10
1.2.4 NITROGEN LIGANDS 13
1.2.5 PALLADACYCLIC COMPLEXES 15
1.3 CROSS-COUPLING IN AQUEOUS MEDIA USING HYDROPHOBIC LIGANDS 17 1.3.1
SURFACTANT-FREE REACTIONS 17
1.3.2 SURFACTANT-PROMOTED REACTIONS 20
1.3.2.1 CATIONIC SURFACTANTS 21
1.3.2.2 ANIONIC SURFACTANTS 22
1.3.2.3 NONIONIC SURFACTANTS 22
1.4 HETEROGENEOUS CATALYSTS I N AQUEOUS MEDIA 25
1.4.1 SUPPORTED PALLADIUM-LIGAND COMPLEXES 2 5 1.4.1.1 POLYMER-SUPPORTED
PALLADIUM COMPLEXES 2 5 1.4.1.2 PALLADIUM COMPLEXES SUPPORTED O N
INORGANIC MATERIALS 2 7 1.4.2 NANOPARTICLE-CATALYZED COUPLING 29 1.4.2.1
UNSUPPORTED PALLADIUM NANOPARTICLE CATALYSTS 29 1.4.2.2
POLYMER-SUPPORTED NANOPARTICLES 30 1.4.2.3 INORGANIC-SUPPORTED
NANOPARTICLE CATALYSTS 33 1.5 SPECIAL REACTION CONDITIONS 35
1.5.1 MICROWAVE HEATING 35
1.5.2 ULTRASOUND 36
1.5.3 THERMOMORPHIC REACTION CONTROL 36
HTTP://D-NB.INFO/1024048225
IMAGE 2
V I CONTENTS
1.6 HOMOGENEOUS AQUEOUS-PHASE MODIFICATION O F BIOMOLECULES 3 7
1.6.1 AMINO ACIDS A N D PROTEINS 3 7
1.6.2 NUCLEOSIDES A N D NUCLEOTIDES 38
1.7 CONCLUSION 3 9
REFERENCES 39
2 METAL-CATALYZED C-H BOND ACTIVATION AND C-C BOND FORMATION IN WATER 4
7
BIN LI AND PIERRE H. DIXNEUF 2.1 INTRODUCTION 47
2.2 CATALYTIC FORMATION O F C - C BONDS FROM S P C - H BONDS I N
WATER 48
2.2.1 CATALYTIC NUCLEOPHILIC ADDITIONS O F ALKYNES IN WATER 48 2.2.2
ADDITION O F TERMINAL ALKYNES TO C = C BONDS I N WATER 49 2.2.3 THE
SONOGASHIRA-TYPE REACTIONS I N WATER 49 2.3 ACTIVATION O F S P 2 C - H
BONDS FOR CATALYTIC C - C BOND FORMATION I N
WATER 53
2.3.1 HOMOCOUPLING O F S P 2 C - H BONDS 53
2.3.2 DIRECT C - H BOND ARYLATION O F ALKENES AND ARYL BORONIC ACID
DERIVATIVES 55 2.3.3 CROSS-COUPLING REACTIONS O F S P 2 C - H BONDS WITH
SP2C-X BONDS I N WATER 56
2.3.3.1 DIRECT C - H BOND ARYLATIONS WITH ARYL HALIDES AND PALLADIUM
CATALYSTS 56 2.3.3.2 DIRECT C - H BOND ARYLATIONS WITH ARYL HALIDES A N
D RUTHENIUM CATALYSTS 62 2.3.4 CROSS-COUPLING REACTIONS O F S P 2 C - H
BONDS WITH CARBON
NUCLEOPHILES IN WATER 64 2.3.5 OXIDATIVE CROSS-COUPLING O F S P 2 C - H
BOND REACTIONS IN WATER 65 2.3.5.1 ALKENYLATIONS O F ARENES A N D
HETEROARENES WITH PALLADIUM CATALYSTS 65
2.3.5.2 ALKENYLATION O F HETEROCYCLES USING IN(OTF )3 CATALYST 6 8
2.3.5.3 ALKENYLATION O F ARENES A N D HETEROARENES WITH RUTHENIUM(II)
CATALYSTS 69
2.4 ACTIVATION O F S P 3 C - H BONDS FOR CATALYTIC C - C BOND FORMATION
I N WATER 73
2.4.1 SELECTIVE S P 3 C - H ACTIVATION O F KETONES 73
2.4.2 CATALYTIC ENANTIOSELECTIVE ALKYNYLATION O F S P 3 C - H BONDS 74
2.4.3 CROSS-DEHYDROGENATIVE COUPLING BETWEEN S P 3 C - H BONDS ADJACENT
T O A HETEROATOM 75
2.4.4 CATALYTIC ENOLATE CARBON COUPLING WITH (ARENE) C-X CARBON 77 2.4.5
ARYLATION O F S P 3 C - H BONDS WITH ARYL HALIDES OR S P 2 C - H BOND 79
2.5 CONCLUSION 80
ACKNOWLEDGMENTS 81 REFERENCES 81
IMAGE 3
CONTENTS V I I
3 CATALYTIC NUCLEOPHILIC ADDITIONS O F ALKYNES IN WATER 87
XIAOQUAN YAO AND CHAO-JUN LI 3.1 INTRODUCTION 87
3.2 CATALYTIC NUCLEOPHILIC ADDITIONS O F TERMINAL ALKYNES WITH CARBONYL
DERIVATIVES 88 3.2.1 REACTION WITH ACID CHLORIDES 89
3.2.2 REACTION WITH ALDEHYDES 89
3.2.3 REACTION WITH KETONES 95
3.3 ADDITION O F TERMINAL ALKYNE TO IMINE, TOSYLIMINE, I M I N I U M
ION, A N D ACYL I M I N I U M ION 96 3.3.1 REACTION WITH IMINES 97
3.3.2 REACTION WITH I M I N I U M IONS 99
3.3.3 REACTION WITH ACYLIMINE A N D ACYLIMINIUM IONS 102 3.4 DIRECT
CONJUGATE ADDITION O F TERMINAL ALKYNES 103
3.5 CONCLUSIONS 105
ACKNOWLEDGMENTS 105 REFERENCES 106
4 WATER-SOLUBLE HYDROFORMYLATION CATALYSIS 109
DUE H A N H NGUYEN, MARTINE URRUTIGOITY, AND PHILIPPE KALCK 4.1
INTRODUCTION 109
4.2 HYDROFORMYLATION O F LIGHT C 2 - C 5 ALKENES I N THE R C H / R P
PROCESS 110
4.3 HYDROFORMYLATION O F ALKENES HEAVIER T H A N C5 115
4.3.1 WATER-SOLUBLE A N D AMPHIPHILIC LIGANDS 116 4.3.2 PHASE-TRANSFER
AGENTS: CYCLODEXTRINS A N D CALIXARENES 120 4.3.3 SUPPORTED
AQUEOUS-PHASE CATALYSIS 125 4.4 INNOVATIVE EXPANSIONS 128
4.4.1 THERMOREGULATED CATALYTIC SYSTEMS 128 4.4.2 IONIC LIQUIDS A N D
CARBON DIOXIDE INDUCED PHASE SWITCHING 129 4.4.3 CASCADE REACTIONS 130
4.5 CONCLUSION 132
REFERENCES 133
5 CREEN CATALYTIC OXIDATIONS IN WATER 139
ROGER A. SHELDON
5.1 INTRODUCTION 139
5.2 EXAMPLES O F WATER-SOLUBLE LIGANDS 140
5.3 ENZYMATIC OXIDATIONS 140
5.4 BIOMIMETIC OXIDATIONS 142
5.5 EPOXIDATION, DIHYDROXYLATION, A N D OXIDATIVE CLEAVAGE O F OLEFINS
143 5.5.1 TUNGSTEN-BASED SYSTEMS 144
5.5.2 MANGANESE- A N D IRON-BASED SYSTEMS 145 5.5.3 RUTHENIUM A N D
PLATINUM CATALYSTS 148
5.5.4 OTHER SYSTEMS 149
IMAGE 4
V I I I I CONTENTS
5.6 ALCOHOL OXIDATIONS 151
5.6.1 TUNGSTEN (VI) CATALYSTS 151
5.6.2 PALLADIUM DIAMINE COMPLEXES AS CATALYSTS 153 5.6.3 NOBLE METAL
NANOPARTICLES AS QUASI-HOMOGENEOUS CATALYSTS 156 5.6.4 RUTHENIUM A N D
MANGANESE CATALYSTS 158
5.6.5 ORGANOCATALYSTS: STABLE N-OXY RADICALS A N D HYPERVALENT IODINE
COMPOUNDS 158 5.6.6 ENZYMATIC OXIDATION O F ALCOHOLS 161 5.7
SULFOXIDATIONS IN WATER 161
5.7.1 TUNGSTEN-AND VANADIUM-CATALYZED OXIDATIONS 162 5.7.2
ENANTIOSELECTIVE SULFOXIDATION WITH ENZYMES 163 5.7.3 FLAVINS AS
ORGANOCATALYSTS FOR SULFOXIDATION 165 5.8 CONCLUSIONS A N D FUTURE
OUTLOOK 166
REFERENCES 166
6 HYDROGENATION AND TRANSFER HYDROGENATION IN WATER 173
XIAOFENG W U AND JIANLIANG XIAO 6.1 INTRODUCTION 173
6.2 WATER-SOLUBLE LIGANDS 174
6.2.1 WATER-SOLUBLE ACHIRAL LIGANDS 175 6.2.2 WATER-SOLUBLE CHIRAL
LIGANDS 175
6.3 HYDROGENATION IN WATER 176
6.3.1 ACHIRAL HYDROGENATION 176
6.3.1.1 HYDROGENATION O F OLEFINS 176 6.3.1.2 HYDROGENATION O F CARBONYL
COMPOUNDS 6.3.1.3 HYDROGENATION O F AROMATIC RINGS 185 6.3.1.4
HYDROGENATION O F OTHER ORGANIC GROUPS 6.3.1.5 HYDROGENATION O F C 0 2
188
6.3.2 ASYMMETRIC HYDROGENATION 191
6.3.2.1 ASYMMETRIC HYDROGENATION O F OLEFINS 191 6.3.2.2 ASYMMETRIC
HYDROGENATION O F CARBONYL AND RELATED COMPOUNDS 194 6.3.2.3 ASYMMETRIC
HYDROGENATION O F IMINES 196 6.4 TRANSFER HYDROGENATION IN WATER 197
6.4.1 ACHIRAL TRANSFER HYDROGENATION 198
6.4.1.1 ACHIRAL TRANSFER HYDROGENATION O F CARBONYL COMPOUNDS 198
6.4.1.2 ACHIRAL TRANSFER HYDROGENATION O F IMINO COMPOUNDS 203 6.4.2
ASYMMETRIC TRANSFER HYDROGENATION 204 6.4.2.1 ASYMMETRIC TRANSFER
HYDROGENATION O F C = C DOUBLE BONDS 204
6.4.2.2 ASYMMETRIC TRANSFER HYDROGENATION O F SIMPLE KETONES 204 6.4.2.3
ASYMMETRIC TRANSFER HYDROGENATION O F FUNCTIONALIZED KETONES 209 6.4.2.4
ASYMMETRIC TRANSFER HYDROGENATION O F IMINES 213 6.4.3 ASYMMETRIC
TRANSFER HYDROGENATION WITH BIOMIMETIC CATALYSTS 219 6.4.4 ASYMMETRIC
TRANSFER HYDROGENATION WITH IMMOBILIZED
" CATALYSTS 222
183
187
IMAGE 5
CONTENTS I X
6.5 ROLE O F WATER 228
6.5.1 COORDINATION TO METALS 228
6.5.2 ACID-BASE EQUILIBRIUM 229
6.5.3 H - D EXCHANGE 230
6.5.4 PARTICIPATION I N TRANSITION STATES 231
6.6 CONCLUDING REMARKS 232
REFERENCES 233
7 CATALYTIC REARRANGEMENTS AND ALLYLATION REACTIONS IN WATER 243
VICTORIO CADIERNO, JOAQUIN GARCIA-ALVAREZ, AND SERGIO E. GARCIA-GARRIDO
7.1 INTRODUCTION 243
7.2 REARRANGEMENTS 244
7.2.1 ISOMERIZATION O F OLEFINIC SUBSTRATES 244
7.2.1.1 ISOMERIZATION O F ALLYLIC ALCOHOLS, ETHERS, A N D AMINES 244
7.2.1.2 ISOMERIZATION O F OTHER OLEFINS 252 7.2.2 CYCLOISOMERIZATIONS A
N D RELATED CYCLIZATION PROCESSES 256 7.2.3 OTHER REARRANGEMENTS 261
7.3 ALLYLATION REACTIONS 264
7.3.1 ALLYLIC SUBSTITUTION REACTIONS 265
7.3.1.1 PALLADIUM-CATALYZED ALLYLIC SUBSTITUTION REACTIONS (TSUJI-TROST
ALLYLATIONS) 265 7.3.1.2 OTHER METAL-CATALYZED ALLYLIC SUBSTITUTION
REACTIONS 272 7.3.2 ALLYLATION REACTIONS O F C = 0 A N D C = N BONDS 273
7.3.3 OTHER ALLYLATION REACTIONS I N AQUEOUS MEDIA 278 7.4 CONCLUSION
279
ACKNOWLEDGMENTS 279 REFERENCES 280
8 ALKENE METATHESIS IN WATER 291
KAROL GRELA, LUKASZ GUIAJSKI, AND KRZYSZTOF SKOWERSKI 8.1 INTRODUCTION
291
8.1.1 GENERAL INTRODUCTION TO OLEFIN METATHESIS 291 8.1.2 METATHESIS O F
WATER-SOLUBLE SUBSTRATES 293 8.1.3 METATHESIS O F WATER-INSOLUBLE
SUBSTRATES 300 8.1.3.1 "ENABLING TECHNIQUES" FOR OLEFIN METATHESIS I N
AQUEOUS MEDIA 300
8.1.3.2 OTHER ADDITIVES A N D TECHNIQUES 305 8.2 EXAMPLES O F
APPLICATIONS O F OLEFIN METATHESIS I N AQUEOUS MEDIA 308
8.2.1 POLYMERIZATIONS 308
8.2.2 METATHESIS O F WATER-SOLUBLE SUBSTRATES 312 8.2.2.1 RING-CLOSING
METATHESIS A N D ENYNE CYCLOISOMERIZATION OF WATER-SOLUBLE SUBSTRATES
312 8.2.2.2 CROSS METATHESIS O F WATER-SOLUBLE SUBSTRATES 315 8.2.3
CROSS METATHESIS WITH SUBSTRATE HAVING A N ALLYLIC HETEROATOM 31 6 8.2.4
METATHESIS O F WATER-INSOLUBLE SUBSTRATES 318
IMAGE 6
X CONTENTS
8.2.4.1 RING-CLOSING METATHESIS O F WATER-INSOLUBLE SUBSTRATES 318
8.2.4.2 ENYNE CYCLOISOMERIZATION 328 8.2.4.3 CROSS METATHESIS
OFWATER-INSOLUBLE SUBSTRATES 328 8.3 CONCLUSIONS A N D OUTLOOK 332
ACKNOWLEDGMENTS 333 REFERENCES 333
9 NANOCATALYSIS IN WATER 337
R. B. NASIR BAIG AND RAJENDER S. VARMA 9.1 INTRODUCTION 337
9.2 NANOCATALYSIS 338
9.3 EFFECTS O F SIZE O F NANOCATALYSTS 339
9.4 TRANSITION-METAL NANOPARTICLES 340
9.4.1 SYNTHESIS O F TRANSITION-METAL NANOPARTICLES 341 9.4.2 GREENER
SYNTHESIS O F NANOMATERIALS 341
9.4.3 IMMOBILIZATION O F M-NPS O N A SOLID SUPPORT 343
9.5 CATALYTIC APPLICATIONS O F TRANSITION-METAL-BASED NANOMATERIALS 343
9.6 P D NANOPARTICLES IN ORGANIC SYNTHESIS 344
9.6.1 P D NANOPARTICLES IN SUZUKI REACTIONS 344
9.6.2 P D NANOPARTICLES IN THE HECK REACTIONS 350
9.6.3 PD NANOPARTICLES I N THE SONOGASHIRA REACTIONS 354 9.6.4 PD
NANOPARTICLES IN THE STILLE COUPLING REACTIONS 359 9.6.5 PD
NANOPARTICLES I N THE HIYAMA COUPLINGS 360
9.6.6 PD NANOPARTICLES IN THE TSUJI-TROST REACTION 361
9.7 NANOGOLD CATALYSIS 362
9.7.1 COUPLING REACTIONS 362
9.7.1.1 THE SUZUKI-MIYAURA CROSS-COUPLING REACTION 362 9.7.1.2
HOMOCOUPLING O F ARYLBORONIC ACID 365 9.7.2 REDUCTION REACTIONS 366
9.7.2.1 HYDROGENATION O F BENZENE 366 9.7.2.2 NITRO GROUP REDUCTION 367
9.7.3 OXIDATION REACTIONS 368
9.7.3.1 BENZYLIC A N D ALLYLIC C - H BONDS OXIDATION 368 9.7.3.2
EPOXIDATION O F PROPYLENE 369 9.7.3.3 OXIDATION O F ALCOHOLS 370
9.7.4 HYDRATION O F ALKYNES 371
9.8 COPPER NANOPARTICLES 372
9.8.1 PHENYLSELENYLATION O F ARYL IODIDES A N D VINYL BROMIDES 372 9.8.2
CUL-NANOPARTICLE-CATALYZED SELECTIVE SYNTHESIS O F PHENOLS, ANILINES, A
N D THIOPHENOLS 373 9.8.3 HYDROGENATION O F AZIDES OVER COPPER
NANOPARTICLES 373
9.8.4 CU-NANOPARTICLE-CATALYZED SYNTHESIS O F ARYL DITHIOCARBAMATE 374
9.8.5 CLICK CHEMISTRY 375
9.9 RUTHENIUM NANOCATALYSTS 376
9.10 MAGNETIC IRON OXIDE NANOPARTICLE 378
IMAGE 7
9.10.1 SYNTHESIS O F HETEROCYDES 378
9.10.2 HOMOCOUPLING O F ARYLBORONIC ACID 381 9.10.3 RH ANCHORED ON FE
304 NANOPARTICLES 382 9.11 COBALT NANOPARTICLES 384
9.12 CONCLUSION 386
REFERENCES 387
INDEX 395 |
| any_adam_object | 1 |
| author2 | Dixneuf, P. H. |
| author2_role | edt |
| author2_variant | p h d ph phd |
| author_GND | (DE-588)1031580603 |
| author_facet | Dixneuf, P. H. |
| building | Verbundindex |
| bvnumber | BV040903660 |
| classification_rvk | VK 5500 VK 5560 |
| classification_tum | CHE 620f CHE 327f |
| ctrlnum | (OCoLC)829310466 (DE-599)DNB1024048225 |
| 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 |
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| genre | (DE-588)4143413-4 Aufsatzsammlung gnd-content |
| genre_facet | Aufsatzsammlung |
| id | DE-604.BV040903660 |
| illustrated | Illustrated |
| indexdate | 2024-08-21T00:37:56Z |
| institution | BVB |
| isbn | 3527331883 9783527331888 9783527656790 |
| language | English |
| oai_aleph_id | oai:aleph.bib-bvb.de:BVB01-025883139 |
| oclc_num | 829310466 |
| open_access_boolean | |
| owner | DE-11 DE-703 DE-91G DE-BY-TUM DE-19 DE-BY-UBM |
| owner_facet | DE-11 DE-703 DE-91G DE-BY-TUM DE-19 DE-BY-UBM |
| physical | XVII, 407 S. Ill., graph. Darst. 25 cm |
| publishDate | 2013 |
| publishDateSearch | 2013 |
| publishDateSort | 2013 |
| publisher | Wiley-VCH-Verl. |
| record_format | marc |
| series2 | Green chemistry |
| spelling | Metal-catalyzed reactions in water ed. by Pierre H. Dixneuf ... Weinheim Wiley-VCH-Verl. 2013 XVII, 407 S. Ill., graph. Darst. 25 cm txt rdacontent n rdamedia nc rdacarrier Green chemistry Literaturangaben Grüne Chemie (DE-588)7563215-9 gnd rswk-swf Wasser (DE-588)4064689-0 gnd rswk-swf Katalyse (DE-588)4029921-1 gnd rswk-swf Organische Synthese (DE-588)4075695-6 gnd rswk-swf Lösungsmittel (DE-588)4036160-3 gnd rswk-swf (DE-588)4143413-4 Aufsatzsammlung gnd-content Organische Synthese (DE-588)4075695-6 s Katalyse (DE-588)4029921-1 s Wasser (DE-588)4064689-0 s Lösungsmittel (DE-588)4036160-3 s Grüne Chemie (DE-588)7563215-9 s DE-604 Dixneuf, P. H. (DE-588)1031580603 edt Erscheint auch als Online-Ausgabe, EPUB 978-3-527-65681-3 Erscheint auch als Online-Ausgabe, MOBI 978-3-527-65680-6 Erscheint auch als Online-Ausgabe, PDF 978-3-527-65682-0 X:MVB text/html http://deposit.dnb.de/cgi-bin/dokserv?id=4071686&prov=M&dok_var=1&dok_ext=htm Inhaltstext DNB Datenaustausch application/pdf http://bvbr.bib-bvb.de:8991/F?func=service&doc_library=BVB01&local_base=BVB01&doc_number=025883139&sequence=000001&line_number=0001&func_code=DB_RECORDS&service_type=MEDIA Inhaltsverzeichnis |
| spellingShingle | Metal-catalyzed reactions in water Grüne Chemie (DE-588)7563215-9 gnd Wasser (DE-588)4064689-0 gnd Katalyse (DE-588)4029921-1 gnd Organische Synthese (DE-588)4075695-6 gnd Lösungsmittel (DE-588)4036160-3 gnd |
| subject_GND | (DE-588)7563215-9 (DE-588)4064689-0 (DE-588)4029921-1 (DE-588)4075695-6 (DE-588)4036160-3 (DE-588)4143413-4 |
| title | Metal-catalyzed reactions in water |
| title_auth | Metal-catalyzed reactions in water |
| title_exact_search | Metal-catalyzed reactions in water |
| title_full | Metal-catalyzed reactions in water ed. by Pierre H. Dixneuf ... |
| title_fullStr | Metal-catalyzed reactions in water ed. by Pierre H. Dixneuf ... |
| title_full_unstemmed | Metal-catalyzed reactions in water ed. by Pierre H. Dixneuf ... |
| title_short | Metal-catalyzed reactions in water |
| title_sort | metal catalyzed reactions in water |
| topic | Grüne Chemie (DE-588)7563215-9 gnd Wasser (DE-588)4064689-0 gnd Katalyse (DE-588)4029921-1 gnd Organische Synthese (DE-588)4075695-6 gnd Lösungsmittel (DE-588)4036160-3 gnd |
| topic_facet | Grüne Chemie Wasser Katalyse Organische Synthese Lösungsmittel Aufsatzsammlung |
| url | http://deposit.dnb.de/cgi-bin/dokserv?id=4071686&prov=M&dok_var=1&dok_ext=htm http://bvbr.bib-bvb.de:8991/F?func=service&doc_library=BVB01&local_base=BVB01&doc_number=025883139&sequence=000001&line_number=0001&func_code=DB_RECORDS&service_type=MEDIA |
| work_keys_str_mv | AT dixneufph metalcatalyzedreactionsinwater |