Modern gold catalyzed synthesis:
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| Format: | Buch |
| Sprache: | English |
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2012
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| Ausgabe: | 1. Aufl. |
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| Beschreibung: | XV, 402 S. graph. Darst. |
| ISBN: | 9783527319527 |
Internformat
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| 245 | 1 | 0 | |a Modern gold catalyzed synthesis |c ed. by A. Stephen K. Hashmi ... |
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| 264 | 1 | |a Weinheim |b Wiley-VCH |c 2012 | |
| 300 | |a XV, 402 S. |b graph. Darst. | ||
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Datensatz im Suchindex
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IMAGE 1
CONTENTS
LIST O F CONTRIBUTORS X I I I
1 HYDROCHLORINATION O F ACETYLENE CATALYZED BY COLD 1
MARCO CONTE A N D GRAHAM J. HUTCHINGS 1.1 INTRODUCTION 1
1.2 REACTIONS O F ALKYNES U S I N G GOLD CHLORIDE AS CATALYST 2
1.3 T H E CORRELATION O F E WITH T H E ACTIVITY O F GOLD FOR T H E
HYDROCHLORINATION O F ACETYLENE 4 1.3.1 T H E INITIAL CORRELATION 4
1.3.2 CONCEPTUAL DEVELOPMENTS O F T H E E CORRELATION 5
1.3.3 FURTHER STUDY O F T H E CORRELATION O F E WITH T H E ACTIVITY
O F P L A T I N U M G R O U P METALS 8 1.3.4 T H E E CORRELATION
APPLIED TO H O M O G E N E O U S A N D
N O N H O M O G E N E O U S GOLD NANOALLOYS 9 1.4 CENTRAL ROLE O F AU"^
A N D REGENERATION O F A U / C CATALYSTS 12
1.5 REACTION M E C H A N I S M O F ALKYNES OVER A U / C CATALYSTS 14
1.5.1 EFFECT O F T H E INDIVIDUAL C O M P O N E N T S O F T H E
REACTANTS TO A U / C 14
1.5.2 REACTION O F H I G H E R ALKYNES OVER A U / C 16
1.5.3 HYDROCHLORINATION O F 1-HEXYNE, PHENYLACETYLENE, A N D 2-HEXYNE
OVER A U / C CATALYST 17 1.5.4 COMPUTATIONAL STUDIES O F T H E REACTION
O F ACETYLENE OVER A U / C 21
1.6 CHEMICAL ORIGIN O F T H E E CORRELATION A N D GENERAL R E M A R K S
2 2
1.7 C O M M E R C I A L PROCESSES A N D ECONOMIC ASPECTS O F
VINYL CHLORIDE M O N O M E R MANUFACTURE 2 4 REFERENCES 2 5
2 COLD-CATALYZED REDUCTION REACTIONS 2 7
AVELINO CORMA AND PEDRO SERNA 2.1 INTRODUCTION 2 7
2.2 HYDROGENATION O F MULTIPLE C = C BONDS. ROLE O F T H E GOLD
OXIDATION STATE 2 8
2.2.1 INTRODUCTION 2 8
HTTP://D-NB.INFO/991677382
IMAGE 2
V I C O N T E N T S
2.2.2 FIRST SOLID GOLD CATALYSTS: F R O M EXTENDED AU SURFACES TO HIGHLY
DISPERSED NANOPARTICLES 28 2.2.3 RECENT ADVANCES I N SUPPORTED GOLD
CHEMISTRY; F R O M HIGHLY DISPERSED NANOPARTICLES TO INDIVIDUAL
SUPPORTED A U A T O M S 3 1 2.2.4 S U M M A R Y 3 4
2.3 HYDROGENATION O F A,(3-UNSATURATED ALDEHYDES 34
2.3.1 INTRODUCTION 3 4
2.3.2 CHEMISTRY O F GOLD NANOPARTICLES: FIRST STUDIES A N D HYPOTHESES
36
2.3.3 STRONG METAL-SUPPORT INTERACTIONS: EFFECT O F ELECTRONIC TRANSFERS
A N D DECORATION O N T H E GOLD NANOPARTICLES 3 7 2.3.4 EFFECT O F
MORPHOLOGICAL FACTORS: SIZE A N D SHAPE 38
2.3.5 S U M M A R Y 3 9
2.4 HYDROGENATION O F SUBSTITUTED NITROAROMATIC C O M P O U N D S 4 1
2.4.1 INTRODUCTION 41
2.4.2 GOLD CATALYSTS FOR T H E PRODUCTION O F SUBSTITUTED NITRO C O M P
O U N D S 4 2
2.4.3 HYDROGENATION O F - N 0 2 G R O U P S O N GOLD CATALYSTS:
REACTION PATHWAY 43 2.4.4 CHEMOSELECTIVITY O F GOLD CATALYSTS FOR T H E
HYDROGENATION O F N 0 2 G R O U P S 4 7
2.4.5 ACTIVITY O F GOLD CATALYSTS FOR T H E HYDROGENATION O F N 0 2 G R
O U P S 4 9
2.4.6 S U M M A R Y 51
REFERENCES 51
3 GOLD-CATALYZED BENZANNULATIONS: ASAO-YAMAMOTO BENZOPYRYLIUM
PATHWAY 5 5
NAOKI ASAO AND YOSHINORI YAMAMOTO
3.1 INTRODUCTION 5 5
3.2 ACETYLENIC C O M P O U N D S AS 2N SYSTEMS 5 6
3.3 ENOLS AS 2 N SYSTEMS 6 0
3.4 ENOL ETHERS AS 2 K S Y S T E M S 62
3.5 BENZYNES AS 2 N SYSTEMS 63
3.6 SYNTHESIS O F PHTHALAZINE DERIVATIVES 64
3.7 APPLICATION TO T H E SYNTHESIS O F ANGUCYCLINONE ANTIBIOTICS
A N D O T H E R APPLICATIONS I N TOTAL SYNTHESIS 6 5 3.8
COPPER-CATALYZED BENZANNULATIONS 6 7
3.9 CONCLUSION 68
REFERENCES 6 9
4 GOLD-CATALYZED REACTIONS O F PROPARGYL ESTERS, PROPARGYL ALCOHOLS, A N
D RELATED C O M P O U N D S 75 PABLO MAULEON AND F. DEAN TOSTE 4.1
INTRODUCTION A N D EXTENT O F T H I S C H A P T E R 75
4.2 PROPARGYL ESTERS 76
IMAGE 3
C O N T E N T S V I I
4.2.1 GENERAL MECHANISTIC CONSIDERATIONS 76
4.2.1.1 [2,3]- A N D [3,3]-REARRANGEMENTS 7 7
4.2.1.2 REVERSIBILITY 7 8
4.2.1.3 IONIZATION 8 0
4.2.1.4 DOUBLE [2,3]-REARRANGEMENTS 83 4.2.2 REACTIONS INITIATED BY
[2,3]-REARRANGEMENTS 8 5
4.2.2.1 T H E RAUTENSTRAUCH R E A R R A N G E M E N T 86
4.2.2.2 ALKENE CYCLOPROPANATIONS 8 7
4.2.2.3 ENANTIOSELECTIVE TRANSFORMATIONS AFTER [2,3]-REARRANGEMENTS 92
4.2.2.4 NUCLEOPHILIC ATTACK O N GOLD CARBENOIDS GENERATED AFTER
[2,3]-REARRANGEMENTS 94 4.2.3 REACTIONS INITIATED B Y
[3,3]-REARRANGEMENTS 96
4.2.3.1 NUCLEOPHILIC DOUBLE BONDS 9 7
4.2.3.2 TRIPLE BONDS 99
4.2.3.3 AROMATIC G R O U P S 100
4.2.3.4 ALKYL G R O U P S 100
4.2.3.5 H E T E R O A T O M S 102
4.2.3.6 ELECTROPHILIC TRAPPING O F VINYL-GOLD INTERMEDIATES 103 4.2.3.7
O T H E R PROCESSES 104
4.3 PROPARGYL ETHERS 107
4.3.1 PROPARGYL VINYL ETHERS 107
4.3.2 PROPARGYL ALKYL ETHERS 110
4.3.3 O T H E R ETHER SUBSTITUTION PATTERNS 113
4.4 PROPARGYL ALCOHOLS 115
4.4.1 ALKYNE HYDRATION 115
4.4.2 MEYER-SCHUSTER REARRANGEMENTS 115
4.4.3 NUCLEOPHILIC SUBSTITUTION AT T H E PROPARGYLIC
POSITION 117
4.4.4 RING EXPANSIONS 117
4.4.5 O T H E R REACTIONS INVOLVING PROPARGYL ALCOHOLS 119
4.5 PROPARGYL A M I N E S 121
4.6 PROPARGYL CARBONATES, AMIDES, A N D CARBAMATES 124
4.7 O T H E R PROPARGYL SUBSTITUTION PATTERNS 127
4.8 CONCLUSION 129
REFERENCES 130
5 INTRAMOLECULAR HYDROARYLATION O F ALKYNES 135
PAULA DE MENDOZA AND ANTONIO M. ECHAVARREN 5.1 INTRODUCTION 135
5.2 INTRAMOLECULAR REACTIONS O F ARENES WITH ALKYNES 137
5.3 INTRAMOLECULAR REACTIONS O F ELECTRON-RICH H E T E R O A R E N E S
WITH ALKYNES 142
5.4 CONCLUSION A N D OUTLOOK 148
REFERENCES 148
IMAGE 4
V I I I C O N T E N T S
6 GOLD-ALKYNE COMPLEXES 153
MARIA AGOSTINA CINELLU
6.1 INTRODUCTION 153
6.2 DESCRIPTION O F T H E M-RT-BOND INTERACTION I N ALKENE A N D ALKYNE
COMPLEXES 154
6.3 GOLD(O) COMPLEXES 155
6.4 GOLD(I) COMPLEXES 155
6.4.1 NEUTRAL DERIVATIVES 155
6.4.2 CATIONIC DERIVATIVES 158
6.4.3 N-COMPLEXATION O F GOLD(I) AT METAL-ALKYNYL UNITS M - C = C - R
164
6.5 GOLD(III) COMPLEXES 167
6.6 THEORETICAL STUDIES 167
REFERENCES 171
7 GOLD-ALKENE COMPLEXES 175
MARIA AGOSTINA CINELLU
7.1 INTRODUCTION 175
7.2 GOLD(O) DERIVATIVES 176
7.3 GOLD(I) COMPLEXES 176
7.3.1 NEUTRAL DERIVATIVES 176
7.3.1.1 14-ELECTRON SPECIES 176
7.3.1.2 16-ELECTRON SPECIES 178
7.3.2 CATIONIC DERIVATIVES 181
7.3.2.1 14-ELECTRON SPECIES 181
7.3.2.2 16-ELECTRON SPECIES 186
7.4 GOLD(III) COMPLEXES 191
7.5 THEORETICAL STUDIES 192
REFERENCES 196
8 HYDRATION A N D HYDROALKOXYLATION O F CC MULTIPLE BONDS 201
J. HENRIQUE TELES
8.1 HISTORICAL PERSPECTIVE 201
8.1.1 ADDITION O F WATER TO ALKYNES 201
8.1.2 ADDITION O F ALCOHOLS TO ALKYNES 2 0 2
8.2 GOLD CATALYSTS 202
8.2.1 FIRST REPORTS O F GOLD CATALYSTS 203
8.2.2 T H E DISCOVERY O F AU(I) CATALYSTS 204
8.2.2.1 CATALYST PRECURSORS 206
8.2.2.2 T H E I M P O R T A N C E O F CHEMICAL EQUILIBRIA 208
8.3 HYDRATION A N D HYDROALKOXYLATION O F C C TRIPLE BONDS (ALKYNES) 209
8.3.1 EFFECT O F ALCOHOL STRUCTURE 209
8.3.2 ADDITION O F WATER TO ALKYNES 211
8.3.3 ADDITION O F ALCOHOLS TO SIMPLE ALKYNES 215
8.3.4 REACTIONS INVOLVING PROPARGYLIC ALCOHOLS 217
8.3.5 ADDITIONS TO HOMOPROPARGYLIC ALCOHOLS A N D O T H E R ALKYNOLS 2 2
0
IMAGE 5
8.3.6
8.4
8.4.1 8.4.2 8.4.3
9
9.1 9.1.1 9.1.1.1 9.1.1.2 9.1.1.3 9.1.1.4 9.1.1.5 9.1.1.6 9.1.1.7 9.1.2
9.1.2.1 9.1.2.2 9.1.3 9.1.3.1 9.1.3.2 9.1.3.3
9.2 9.2.1 9.2.2 9.2.3
10
10.1 10.2
10.3
10.4 10.5
11
11.1 11.2
C O N T E N T S I X
REACTIONS INVOLVING PROPARGYLIC ETHERS 224
HYDRATION A N D HYDROALKOXYLATION O F CC DOUBLE BONDS (ALLENES A N D
ALKENES) 226 ADDITION O F ALCOHOLS TO ALLENES 226 CYCLIZATION O F
ALLENYL A N D PROPARGYL KETONES 2 2 7
ADDITION O F ALCOHOLS TO ALKENES 230
REFERENCES 234
COLD-CATALYZED ALDOL A N D RELATED REACTIONS 237
CHRISTOPH HUBBERT AND A. STEPHEN K. HASHMI T H E GOLD-CATALYZED ALDOL
REACTION 237 SYNTHETIC SCOPE 239 REACTIONS O F ALDEHYDES WITH METHYL
ISOCYANOACETATE 239
REACTIONS O F ALDEHYDES WITH A-SUBSTITUTED ISONITRILES 241 REACTIONS O F
ALDEHYDES WITH ALKYL ISOCYANOACETATES 242 REACTIONS O F ALDEHYDES WITH
ALKYL ISOCYANOACETAMIDES 243 REACTIONS O F ALDEHYDES WITH A-ISOCYANO W E
I N R E B A M I D E 244
REACTIONS O F ALDEHYDES WITH ISOCYANO P H O S P H O N A T E S 245
REACTIONS O F ALDEHYDES WITH A-KETO ESTERS 246
STRUCTURE O F T H E LIGAND 247
INTERNAL COOPERATIVITY O F CHIRALITY 2 4 8 C O N F O R M A T I O N O F T
H E P E N D A N T SIDE C H A I N 251 MECHANISTIC ASPECTS 253 T H E FIRST
TRANSITION-STATE MODEL 253
STRUCTURE O F T H E FERROCENYL-GOLD(I) COMPLEX 253 MECHANISTIC ASPECTS
253 RELATED REACTIONS 257 SYNTHESIS O F DIHYDROIMIDAZOLE 2 5 7
M A N N I C H REACTIONS 258 MICHAEL REACTIONS 259 REFERENCES 260
COLD-CATALYZED OXIDATION REACTIONS: OXIDATION O F ALKENES 263 YUANHONG
LIU INTRODUCTION 263
EPOXIDATION REACTIONS 263 AZIRIDINATION REACTIONS 2 6 8 OXIDATIVE
CLEAVAGE O F C = C DOUBLE BONDS 269 OXYGEN TRANSFER TO CARBENOIDS 270
REFERENCES 271
COLD-CATALYZED OXYGEN-ATOM TRANSFER T O ALKYNES 273 MARIA CAMILA BLANCO
JAIMES AND A. STEPHEN K. HASHMI INTRODUCTION 273
OXYGEN-ATOM TRANSFER F R O M N O G R O U P S 273
IMAGE 6
X C O N T E N T S
11.2.1 NITRONES 274
11.2.2 NITRO C O M P O U N D S 276
11.2.3 N-OXIDES 277
11.3 OXYGEN-ATOM TRANSFER F R O M SULFOXIDES 280
11.4 OXYGEN-ATOM TRANSFER F R O M EPOXIDES 282
11.5 GOLD-CATALYZED OXIDATIVE COUPLING 283
11.5.1 INTRODUCTION 283
11.5.2 FUNCTIONALIZATION O F C ( S P 2 ) - H BONDS 284
11.5.3 GOLD-CATALYZED NUCLEOPHILIC ADDITION-OXIDATIVE COUPLING REACTIONS
287
REFERENCES 295
12 COLD-CATALYZED ADDITIONS T O ALKENES: N-NUCLEOPHILES 2 9 7
ZIGANG LI, DAVID A. CAPRETTO, AND CHUAN HE REFERENCES 3 0 2
13 COLD-CATALYZED ADDITIONS T O ALKENES: O-NUDEOPHILES 303
ZIGANG LI, DAVID A. CAPRETTO, AND CHUAN HE REFERENCES 3 0 7
14 OXIDATION O F ALCOHOLS A N D CARBOHYDRATES 309
CRISTINA DELIA PINA, ERMELINDA FALLETTA, AND MICHELE ROSSI 14.1
INTRODUCTION 309
14.2 SELECTIVE OXIDATION O F ALCOHOLS 3 1 0
14.2.1 CATALYST PREPARATION 311
14.2.2 OXIDATION O F DIOLS 3 1 2
14.2.3 OXIDATION O F O T H E R POLYOLS 315
14.2.3.1 GLYCEROL 315
14.2.3.2 SORBITOL 317
14.2.3.3 O T H E R ALCOHOLS 3 1 7
14.2.3.4 A M I N O ALCOHOLS 318
14.3 SELECTIVE OXIDATION O F CARBOHYDRATES 3 2 0
14.3.1 OXIDATION O F GLUCOSE TO S O D I U M GLUCONATE 321
14.3.1.1 KINETICS A N D MODELING 323
14.3.2 SYNTHESIS O F FREE GLUCONIC ACID 325
14.4 FUTURE APPLICATIONS 326
14.5 CONCLUSION 327
REFERENCES 328
15 APPLICATIONS O F COLD-CATALYZED REACTIONS T O NATURAL
PRODUCT SYNTHESIS 331 MATTHIAS RUDOLPH 15.1 * INTRODUCTION 331
15.2 ADDITION O F H E T E R O A T O M NUCLEOPHILES TO ALKYNES 3 3 2
15.2.1 HYDRATION O F ALKYNES: PTEROSIN B A N D C 3 3 2
15.2.2 T A N D E M REACTION INCLUDING HYDRATION O F ALKYNES,
ELIMINATION, A N D
CONJUGATE ADDITION: (+)-ANDRACHCINIDINE 3 3 2
IMAGE 7
C O N T E N T S X I
15.2.3 HYDROALKOXYLATION O F ALKYNES: BRYOSTATIN 16 333
15.2.4 BIS-SPIROLCETALIZATION O F ALKYNES: A - D RING O F AZASPIRACID A
N D (-)-USHIKULIDE A 3 3 4 15.2.5 INTRAMOLECULAR H Y D R O A M I N A T I
O N O F C - C TRIPLE BONDS: SOLENOPSIN A, C O M U N E S I N B,
MERSICARPINE, A N D NITIDINE 336 15.3 ADDITION O F H E T E R O A T O M
NUCLEOPHILES TO ALLENES 339
15.3.1 INTERMOLECULAR HYDROALKOXYLATION O F ALLENES: CITREOVIRAL,
(-)-ISOCYCLOCAPITELINE, (-)-ISOCHRYSOTRICINE, A N D BEJAROL 3 3 9 15.3.2
INTERMOLECULAR H Y D R O A M I N A T I O N O F ALLENES: SWAINSONINE 341
15.3.3 INTERMOLECULAR HYDROARYLATION O F ALLENES: (-)-RHAZINILAM 3 4 2
15.4 CYCLOADDITIONS VIA PYRYLIUM INTERMEDIATES F R O M
O-ALKYNYLACYLARENES 343 15.5 REARRANGEMENTS O F PROPARGYL ESTERS 346
15.5.1 1,2-ACYL SHIFT O F PROPARGYL ESTERS: A-DIAZOKETONE EQUIVALENTS 3
4 6 15.5.2 1,3-ACYL SHIFT O F PROPARGYL ESTERS A N D S U B S E Q U E N T
T A N D E M CYCLIZATION O F ENE VINYLALLENES: A 9(12)-CAPNELLENE 347
15.6 SKELETAL R E A R R A N G E M E N T O F 3-BUTYNYL-N-OXIDES:
()-CERMIZINE
A N D (+)-LENTIGINOSINE 349 15.7 ENYNE CYCLIZATIONS 350
15.7.1 SILYLENOL ETHERS AS NUCLEOPHILES: PLATENCIN, (+)-LYCOPALADIN A, A
N D (+)-FAWCETTIMINE 3 5 0 15.7.2 IODOALKYNES I N ENYNE CYCLIZATIONS:
(+)-LYCOPLADINE A 351 15.7.3 FURAN-YNE CYCLIZATION: ()-JUNGIANOL 3 5 2
15.7.4 T A N D E M PROCESS O F ENYNE R E A R R A N G E M E N T A N D P R
I N S CYCLIZATION: (+)-ORIENTALOL A N D (-)-ENGLERIN A 3 5 3 15.7.5 T A
N D E M ENYNE CYCLOISOMERIZATION A N D SEMIPINACOL R E A R R A N G E M E
N T :
VENTRICOS-7(13)-ENE 355 15.8 PROPARGYL CLAISEN REARRANGEMENT:
AZADIRACHTIN 356
15.9 GOLD-CATALYZED C - H ACTIVATION: ( I ) - P T E R O C A R P A N A N
D CRASSIFOLONE 356 15.10 GOLD-CATALYZED ALLYLIC AMINATION:
()-ANGUSTUREINE 358 15.11 CATALYTIC A S Y M M E T R I C ALDOL REACTION
O F ISOCYANOACETATES A N D ALDEHYDES 359
REFERENCES 361
16 COLD-CATALYZED ADDITION REACTIONS T O ALLENES 363
CHRISTIAN WINTER A N D NORBERT KRAUSE 16.1 INTRODUCTION 363
16.2 ADDITION O F H E T E R O A T O M NUCLEOPHILES 363
16.2.1 ADDITION O F OXYGEN NUCLEOPHILES 3 6 4
16.2.2 ADDITION O F NITROGEN NUCLEOPHILES 376
16.2.3 ADDITION O F SULFUR NUCLEOPHILES 381
16.3 ADDITION O F C A R B O N NUCLEOPHILES 3 8 2
16.4 CONCLUSION 386
REFERENCES 3 8 6
INDEX 391 |
| any_adam_object | 1 |
| author2 | Hashmi, A. Stephen K. 1963- |
| author2_role | edt |
| author2_variant | a s k h ask askh |
| author_GND | (DE-588)101199576X |
| author_facet | Hashmi, A. Stephen K. 1963- |
| building | Verbundindex |
| bvnumber | BV040120081 |
| classification_rvk | VE 7040 |
| classification_tum | CHE 330f CHE 369f CHE 167f |
| ctrlnum | (OCoLC)795554548 (DE-599)DNB991677382 |
| dewey-full | 546.656595 547.215 |
| dewey-hundreds | 500 - Natural sciences and mathematics |
| dewey-ones | 546 - Inorganic chemistry 547 - Organic chemistry |
| dewey-raw | 546.656595 547.215 |
| dewey-search | 546.656595 547.215 |
| dewey-sort | 3546.656595 |
| dewey-tens | 540 - Chemistry and allied sciences |
| discipline | Chemie / Pharmazie Physik Chemie |
| edition | 1. Aufl. |
| format | Book |
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| id | DE-604.BV040120081 |
| illustrated | Illustrated |
| indexdate | 2024-07-21T00:31:41Z |
| institution | BVB |
| isbn | 9783527319527 |
| language | English |
| oai_aleph_id | oai:aleph.bib-bvb.de:BVB01-024976191 |
| oclc_num | 795554548 |
| open_access_boolean | |
| owner | DE-11 DE-91G DE-BY-TUM DE-29T DE-92 |
| owner_facet | DE-11 DE-91G DE-BY-TUM DE-29T DE-92 |
| physical | XV, 402 S. graph. Darst. |
| publishDate | 2012 |
| publishDateSearch | 2012 |
| publishDateSort | 2012 |
| publisher | Wiley-VCH |
| record_format | marc |
| spelling | Modern gold catalyzed synthesis ed. by A. Stephen K. Hashmi ... 1. Aufl. Weinheim Wiley-VCH 2012 XV, 402 S. graph. Darst. txt rdacontent n rdamedia nc rdacarrier Katalyse (DE-588)4029921-1 gnd rswk-swf Organische Synthese (DE-588)4075695-6 gnd rswk-swf Gold (DE-588)4157819-3 gnd rswk-swf Gold (DE-588)4157819-3 s Organische Synthese (DE-588)4075695-6 s Katalyse (DE-588)4029921-1 s DE-604 Hashmi, A. Stephen K. 1963- (DE-588)101199576X edt text/html http://deposit.dnb.de/cgi-bin/dokserv?id=3191886&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=024976191&sequence=000001&line_number=0001&func_code=DB_RECORDS&service_type=MEDIA Inhaltsverzeichnis |
| spellingShingle | Modern gold catalyzed synthesis Katalyse (DE-588)4029921-1 gnd Organische Synthese (DE-588)4075695-6 gnd Gold (DE-588)4157819-3 gnd |
| subject_GND | (DE-588)4029921-1 (DE-588)4075695-6 (DE-588)4157819-3 |
| title | Modern gold catalyzed synthesis |
| title_auth | Modern gold catalyzed synthesis |
| title_exact_search | Modern gold catalyzed synthesis |
| title_full | Modern gold catalyzed synthesis ed. by A. Stephen K. Hashmi ... |
| title_fullStr | Modern gold catalyzed synthesis ed. by A. Stephen K. Hashmi ... |
| title_full_unstemmed | Modern gold catalyzed synthesis ed. by A. Stephen K. Hashmi ... |
| title_short | Modern gold catalyzed synthesis |
| title_sort | modern gold catalyzed synthesis |
| topic | Katalyse (DE-588)4029921-1 gnd Organische Synthese (DE-588)4075695-6 gnd Gold (DE-588)4157819-3 gnd |
| topic_facet | Katalyse Organische Synthese Gold |
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