Isocyanide chemistry: applications in synthesis and material science
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Weinheim
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2012
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| Item Description: | Literaturangaben |
| Physical Description: | XVIII, 605 S. Ill., graph. Darst. 25 cm |
| ISBN: | 9783527330430 3527330437 9783527652563 9783527652556 9783527652549 9783527652532 |
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| 245 | 1 | 0 | |a Isocyanide chemistry |b applications in synthesis and material science |c ed. by Valentine Nenajdenko |
| 264 | 1 | |a Weinheim |b Wiley-VCH |c 2012 | |
| 300 | |a XVIII, 605 S. |b Ill., graph. Darst. |c 25 cm | ||
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IMAGE 1
CONTENTS
PREFACE X I I I
LIST O F CONTRIBUTORS X V
1 CHIRAL NONRACEMIC ISOCYANIDES 1
LUCA BANFI, ANDREA BASSO, AND RENATA RIVA 1.1 I N T R O D U C T I O N 1
1.2 SIMPLE U N F U N C T I O N A L I Z E D ISOCYANIDES 1
1.3 ISOCYANIDES C O N T A I N I N G CARBOXYLIC, SULFONYL, O R P H O S P
H O N Y L G R O U P S 4
1.3.1 A-ISOCYANO ESTERS 4
1.3.2 A-ISOCYANO A M I D E S 7
1.3.3 O T H E R ISOCYANO ESTERS O R A M I D E S 9
1.3.4 CHIRAL SULFONYLMETHYL O R P H O S P H O N Y L M E T H Y L
ISOCYANIDES 10 1.4 ISOCYANIDES C O N T A I N I N G A M I N O O R
ALCOHOLIC FUNCTIONALITIES 11
1.4.1 CHIRAL A M I N O O R AZIDO ISOCYANIDES 11
1.4.2 CHIRAL HYDROXY ISOCYANIDES 12
1.5 NATURAL ISOCYANIDES 16
1.5.1 ISOLATION A N D NATURAL SOURCES 16
1.5.2 SYNTHESIS O F NATURALLY O C C U R R I N G ISOCYANIDES 17
1.6 ISOCYANIDES U S E D I N T H E SYNTHESIS O F CHIRAL POLYISOCYANIDES 2
3
1.6.1 PROPERTIES 2 4
1.6.2 SYNTHESIS 2 5
1.6.3 APPLICATIONS 26
REFERENCES 26
2 GENERAL ASPECTS O F ISOCYANIDE REACTIVITY 3 5
MAXIM A. MIRONOF
2.1 INTRODUCTION 3 5
2.2 ISOCYANIDE-CYANIDE R E A R R A N G E M E N T 3 7
2.3 OXIDATION/REDUCTION O F T H E ISOCYANO G R O U P 41
2.3.1 OXIDATION O F T H E ISOCYANO G R O U P 4 1
2.3.2 REACTIONS WITH SULFUR A N D S E L E N I U M 43
HTTP://D-NB.INFO/1019094532
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V I C O N T E N T S
2.3.3 REDUCTION O F T H E ISOCYANO G R O U P 4 5
2.4 REACTIONS O F ISOCYANIDES W I T H ELECTROPHILES 4 7
2.4.1 REACTION W I T H ACIDS 4 9
2.4.2 REACTIONS WITH H A L O G E N S A N D ACYL HALIDES 5 2
2.4.3 REACTIONS W I T H ACTIVATED ALKENES A N D ALKYNES 5 5
2.4.4 REACTIONS W I T H CARBONYL C O M P O U N D S A N D I M I N E S 5 8
2.4.5 REACTIONS W I T H ACTIVATED H E T E R O C U M U L E N S 6 0
2.5 REACTIONS O F ISOCYANIDES WITH NUCLEOPHILES 6 2
2.5.1 REACTIONS W I T H ORGANOMETALLIC C O M P O U N D S 62
2.5.2 REACTIONS W I T H HYDROXIDE, ALCOHOLS, A N D A M I N E S 6 4
2.6 CONCLUSIONS 66
REFERENCES 6 7
3 A-ACIDIC ISOCYANIDES IN MULTICOMPONENT CHEMISTRY 75
NIELS ELDERS, EELCO RUIJTER, VALENTINE C. NENAJDENKO, A N D ROMANO V.A.
ORRU
3.1 I N T R O D U C T I O N 7 5
3.2 SYNTHESIS O F A-ACIDIC ISOCYANIDES 76
3.3 REACTIVITY O F A-ACIDIC ISOCYANIDES 7 8
3.4 M C R S INVOLVING A-ACIDIC ISOCYANIDES 8 0
3.4.1 V A N L E U S E N I M I D A Z O L E M C R 81
3.4.2 2,6,7-TRISUBSTITUTED QUINOXALINE M C R 8 2
3.4.3 4,5-DISUBSTITUTED OXAZOLE M C R 83
3.4.4 NITROPYRROLE M C R 83
3.4.5 2,4,5-TRISUBSTITUTED OXAZOLE M C R 8 4
3.4.5.1 2,4,5-TRISUBSTITUTED OXAZOLES 84 3.4.5.2 VARIATIONS O N T H E
2,4,5-TRISUBSTITUTED OXAZOLE M C R 8 6 3.4.5.3 OXAZOLE M C R A N D
IN-SITU D O M I N O PROCESSES 8 8
3.4.6 2-IMIDAZOLINE M C R 91
3.4.6.1 2-IMIDAZOLINE M C R I N T H E U N I O N O F M C R S 93
3.4.7 DIHYDROPYRIDONE M C R 95
3.5 CONCLUSIONS 9 7
REFERENCES 98
4 SYNTHETIC APPLICATION O F ISOCYANOACETIC ACID DERIVATIVES 109
ANTON V. CULEVICH, ALEXANDER C. ZHDANKO, ROMANO V.A. ORRU, AND VALENTINE
C. NENAJDENKO 4.1 I N T R O D U C T I O N 109
4.2 SYNTHESIS O F A-ISOCYANOACETATE DERIVATIVES 109
4.3 ALKYLATION O F ISOCYANOACETIC ACID DERIVATIVES 113
4.4 A-ISOCYANOACETATES A S MICHAEL D O N O R S 115
4.5 REACTION O F ISOCYANOACETIC ACIDS W I T H ALKYNES: SYNTHESIS O F
PYRROLES 119
4.6 REACTION O F ISOCYANOACETIC ACID DERIVATIVES W I T H CARBONYL
C O M P O U N D S A N D I M I N E S 121
4.6.1 ALDOL-TYPE REACTION O F ISOCYANOACETIC ACIDS W I T H ALDEHYDES:
SYNTHESIS O F OXAZOLINES 122
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C O N T E N T S | V I I
4.6.2 T R A N S I T I O N METAL-CATALYZED ALDOL-TYPE REACTIONS 124
4.6.3 REACTION O F ISOCYANOACETIC ACIDS W I T H IMINES: I M I D A Z O L
I N E F O R M A T I O N 126
4.7 REACTION W I T H ACYLATING AGENTS 129
4.8 M U L T I C O M P O N E N T REACTIONS O F ISOCYANOACETIC
ACID DERIVATIVES 133
4.9 C H E M I S T R Y O F ISOCYANOACETATES BEARING A N ADDITIONAL
FUNCTIONAL
G R O U P 134
4.10 REACTIONS O F ISOCYANOACETIC ACIDS W I T H SULFUR ELECTROPHILES 138
4.11 MISCELLANEOUS REACTIONS 139
4.12 C O N C L U D I N G R E M A R K S 144
4.13 NOTES A D D E D I N P R O O F 145
REFERENCES 145
5 UGI A N D PASSERINI REACTIONS WITH CARBOXYLIC
ACID SURROGATES 159 LAURENT EL KAIM AND LAURENCE CRIMAUD 5.1 I N T R O D
U C T I O N 159
5.2 CARBOXYLIC ACID SURROGATES 160
5.2.1 THIOCARBOXYLIC ACIDS 160
5.2.2 CARBONIC ACID A N D DERIVATIVES 163
5.2.3 SELENIDE A N D SULFIDE 165
5.2.4 SILANOL 165
5.2.5 ISOCYANIC ACID A N D DERIVATIVES 166
5.2.6 HYDRAZOIC ACID 167
5.2.7 P H E N O L S A N D DERIVATIVES 171
5.2.8 C Y A N A M I D E 179
5.3 U S E O F M I N E R A L A N D LEWIS ACIDS 180
5.3.1 UGI A N D PASSERINI REACTIONS TRIGGERED BY MINERAL ACIDS 181
5.3.2 UGI A N D PASSERINI REACTIONS TRIGGERED BY LEWIS ACIDS 184
5.4 CONCLUSIONS 189
REFERENCES 189
6 AMINE (IMINE) C O M P O N E N T SURROGATES IN T H E UGI REACTION A N D
RELATED
ISOCYANIDE-BASED MULTICOMPONENT REACTIONS 195 MIKHAIL KRASAVIN 6.1
INTRODUCTION 195
6.2 HYDROXYLAMINE C O M P O N E N T S I N T H E U G I REACTION 196
6.3 H Y D R A Z I N E C O M P O N E N T S I N T H E UGI REACTION 2 0 0
6.4 MISCELLANEOUS A M I N E SURROGATES FOR T H E U G I REACTION 218
6.5 ACTIVATED AZINES I N REACTIONS W I T H ISOCYANIDES 220
6.6 E N A M I N E S , M A S K E D I M I N E S , A N D CYCLIC I M I N E S
I N T H E
UGI REACTION 223
6.7 C O N C L U D I N G R E M A R K S 2 2 7
ACKNOWLEDGMENTS 227 REFERENCES 227
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V I I I J C O N T E N T S
7 MULTIPLE MULTICOMPONENT REACTIONS WITH ISOCYANIDES 233
LUDGER A. WESSJOHANN, RICARDO A.W. NEVES FILHO, AND DANIEL C. RIVERA
7.1 I N T R O D U C T I O N 233
7.2 O N E - P O T MULTIPLE IMCRS 234
7.2.1 SYNTHESIS O F MULTIVALENT GLYCOCONJUGATES 236
7.2.2 SYNTHESIS O F H Y B R I D P E P T I D E - P E P T O I D P O D A N
D S 237
7.2.3 COVALENT MODIFICATION A N D I M M O B I L I Z A T I O N O F
PROTEINS 2 4 0
7.2.4 A S S E M B L Y O F POLYSACCHARIDE NETWORKS AS SYNTHETIC HYDROGELS
241 7.2.5 SYNTHESIS O F MACROMOLECULES B Y M U L T I C O M P O N E N T
POLYMERIZATION 243 7.3 ISOCYANIDE-BASED MULTIPLE M U L T I C O M P O N E
N T MACROCYCLIZATIONS 243 7.3.1 SYNTHESIS O F H Y B R I D MACROCYCLES B
Y DOUBLE UGI-4CR-BASED
MACROCYCLIZATIONS 244 7.3.2 SYNTHESIS O F MACROBICYCLES BY THREEFOLD
UGI-4CR-BASED
MACROCYCLIZATION 2 4 6 7.4 SEQUENTIAL ISOCYANIDE-BASED M C R S 248
7.4.1 SEQUENTIAL APPROACHES T O LINEAR A N D B R A N C H E D SCAFFOLDS
248
7.4.2 SEQUENTIAL APPROACHES TO MACROCYCLES 254
7.4.3 C O N V E R G E N T A P P R O A C H TO NATURAL P R O D U C T M I M
I C S 256
7.5 CONCLUSIONS 2 5 7
REFERENCES 258
8 ZWITTERIONS A N D ZWITTERION-TRAPPING AGENTS IN ISOCYANIDE
CHEMISTRY 263
A H M A D SHAABANI, AFSHIN SARVARY, AND ALI MALEKI
8.1 I N T R O D U C T I O N 263
8.2 G E N E R A T I O N O F ZWITTERIONIC SPECIES B Y T H E ADDITION O F
ISOCYANIDES T O
ALKYNES 2 6 5
8.2.1 CH-ACIDS AS ZWITTERION-TRAPPING AGENTS 2 6 6
8.2.2 NH-ACIDS AS ZWITTERION-TRAPPING A G E N T S 271
8.2.3 OH-ACIDS AS ZWITTERION-TRAPPING AGENTS 273
8.2.4 CARBONYL C O M P O U N D S AS ZWITTERION-TRAPPING A G E N T S 2 7
5
8.2.5 I M I N E C O M P O U N D S AS ZWITTERION-TRAPPING AGENTS 278
8.2.6 ELECTRON-DEFICIENT OLEFINS AS ZWITTERION-TRAPPING A G E N T S 2 7
9 8.2.7 MISCELLANEOUS C O M P O U N D S AS ZWITTERION-TRAPPING AGENTS 2
8 0
8.3 G E N E R A T I O N O F ZWITTERIONIC SPECIES B Y T H E ADDITION O F
ISOCYANIDES T O
ARYNES 283
8.4 G E N E R A T I O N O F ZWITTERIONIC SPECIES BY T H E ADDITION O F
ISOCYANIDES T O
ELECTRON-DEFICIENT OLEFINS 284 8.5 MISCELLANEOUS REPORTS FOR T H E G E N
E R A T I O N O F ZWITTERIONIC
SPECIES 286
8.6 ISOCYANIDES AS ZWITTERION-TRAPPING AGENTS 287
8.7 CONCLUSIONS 289
A C K N O W L E D G M E N T S 289 REFERENCES 2 8 9
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C O N T E N T S I X
9 RECENT PROGRESS IN NONCLASSICAL ISOCYANIDE-BASED MCRS 2 9 9
ROSARIO RAMON, NICOLA KIELLAND, AND RODOLFO LAVILLA 9.1 INTRODUCTION 2 9
9
9.2 TYPE I MCRS: ISOCYANIDE ATTACK O N ACTIVATED SPECIES 300
9.3 TYPE II MCRS: ISOCYANIDE ACTIVATION 308
9.4 TYPE III MCRS: F O R M A L ISOCYANIDE I N S E R T I O N PROCESSES
320
9.5 CONCLUSIONS 3 2 7
A C K N O W L E D G M E N T S 3 2 7 REFERENCES 3 2 7
10 APPLICATIONS O F ISOCYANIDES IN IMCRS FOR T H E RAPID GENERATION O F
MOLECULAR DIVERSITY 3 3 5 M U H A M M A D AYAZ, FABIO DE MOLINER, JUSTIN
DIETRICH, AND CHRISTOPHER HULME 10.1 I N T R O D U C T I O N 3 3 5
10.2 UGI/DEPROTECT/CYCLIZE (UDC) METHODOLOGY 3 3 7
10.2.1 UGI-4CC: O N E INTERNAL NUCLEOPHILE 337
10.2.2 TMSN 3-MODIFIED UGI-4CC: O N E INTERNAL NUCLEOPHILE 343 10.2.3
UGI-4CC: T W O INTERNAL NUCLEOPHILES 344
10.2.4 UGI-4CC: T H R E E I N T E R N A L NUCLEOPHILES 3 4 7
10.2.5 UGI-5CC: O N E INTERNAL NUCLEOPHILE 348
10.3 SECONDARY REACTIONS O F U G I PRODUCTS 3 5 0
10.3.1 NUCLEOPHILIC ADDITIONS A N D SUBSTITUTIONS 351
10.3.1.1 ALKYLATIONS 351
10.3.1.2 M I T S U N O B U REACTIONS 3 5 2
10.3.1.3 LACTONIZATION A N D LACTAMIZATION 354 10.3.2 BASE- O R
ACID-PROMOTED C O N D E N S A T I O N S 3 5 5
10.3.3 NUCLEOPHILIC A R O M A T I C SUBSTITUTIONS 3 5 5
10.3.4 PALLADIUM-MEDIATED REACTIONS 3 5 6
10.3.5 RING-CLOSING METATHESES 3 5 8
10.3.6 STAUDINGER-AZA-WITTIG REACTIONS 358
10.3.7 CYCLOADDITIONS 3 5 9
10.4 T H E BIFUNCTIONAL A P P R O A C H (BIFA) 361
10.4.1 APPLICATIONS O F A M I N O ACIDS 3 6 3
10.4.2 APPLICATIONS O F CYCLIC I M I N E S 3 6 5
10.4.3 APPLICATIONS O F T E T H E R E D ALDEHYDE A N D KETO ACIDS 3 6 6
10.4.4 HETEROCYCLIC A M I D I N E S AS A T E T H E R E D U G I I N P U T
371
10.4.5 C O M B I N E D BIFUNCTIONAL A N D POST-CONDENSATION
MODIFICATIONS 3 7 2
A C K N O W L E D G M E N T S 3 75 ABBREVIATIONS 3 75 REFERENCES 3 7 6
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X | C O N T E N T S
11 SYNTHESIS O F PYRROLES A N D THEIR DERIVATIVES FROM ISOCYANIDES 3 8 5
NOBORU ONO AND TETSUO OKUJIMA 11.1 I N T R O D U C T I O N 3 8 5
11.2 SYNTHESIS O F PYRROLES U S I N G T O S M I C 386
11.3 SYNTHESIS O F PYRROLES U S I N G ISOCYANOACETATES 391
11.3.1 SYNTHESIS F R O M NITROALKENES 391
11.3.2 SYNTHESIS F R O M A,(3-UNSATURATED SULFONES 396
11.3.3 SYNTHESIS F R O M ALKYNES 401
11.3.4 SYNTHESIS F R O M AROMATIC NITRO C O M P O U N D S : ISOINDOLE
DERIVATIVES 4 0 2
11.4 SYNTHESIS O F P O R P H Y R I N S A N D RELATED C O M P O U N D S
407
11.4.1 T E T R A M E R I Z A T I O N 407
11.4.2 MESO-TETRAARYLPORPHYRINS VIA T H E LINDSEY P R O C E D U R E 4 1
2 11.4.3 [3+2] A N D [2+2] M E T H O D S 4 1 4
11.4.4 EXPANDED, CONTRACTED, A N D ISOMERIC P O R P H Y R I N S 4 1 4
11.4.5 FUNCTIONAL DYES F R O M PYRROLES 4 2 0
11.5 C O N C L U S I O N 423
REFERENCES 4 2 4
12 ISOCYANIDE-BASED MULTICOMPONENT REACTIONS T O W A R D S
BENZODIAZEPINES 431 YIJUN HUANG AND ALEXANDER DOMLING 12.1 I N T R O D U
C T I O N 431
12.2 1,4-BENZODIAZEPINE SCAFFOLDS A S S E M B L E D VIA I M C R C H E M
I S T R Y 4 3 3 12.2.1 TWO-RING SYSTEMS 433
12.2.2 FUSED-RING SYSTEMS 4 4 0
12.3 1,5-BENZODIAZEPINE SCAFFOLDS A S S E M B L E D VIA I M C R C H E M
I S T R Y 443 12.4 OUTLOOK 446
REFERENCES 446
13 APPLICATIONS O F ISOCYANIDES IN T H E SYNTHESIS O F HETEROCYCLES 451
IRINI AKRITOPOULOU-ZANZE 13.1 INTRODUCTION 451
13.2 F U R A N S 451
13.3 PYRROLES 453
13.4 OXAZOLES 459
13.5 ISOXAZOLES 461
13.6 THIAZOLES 4 6 4
13.7 IMIDAZOLES 466
13.8 PYRAZOLES 466
13.9 OXADIAZOLES A N D TRIAZOLES 4 7 0
13.10 TETRAZOLES 471
13.11 BENZOFURANS A N D BENZIMIDAZOLES 473
13.12 INDOLES 473
13.13 Q U I N O L I N E S 4 7 7
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C O N T E N T S | X I
13.14 QUINOXALINE 4 7 9
ABBREVIATIONS 480 REFERENCES 4 8 0
14 RENAISSANCE O F ISOCYANOARENES A S LIGANDS IN LOW-VAIENT
ORGANOMETALLICS 493 MIKHAIL V. BARYBIN, JOHN J. MEYERS, JR, AND BRAD M.
NEAL 14.1 HISTORICAL PERSPECTIVE 493
14.2 ISOCYANIDEMETALATES A N D RELATED LOW-VALENT COMPLEXES 4 9 7 14.2.1
INTRODUCTION 4 9 7
14.2.2 FOUR-COORDINATE ISOCYANIDEMETALATES A N D REDOX-RELATED
COMPLEXES 4 9 7
14.2.3 FIVE-COORDINATE ISOCYANIDEMETALATES 5 0 2 14.2.4 SIX-COORDINATE
ISOCYANIDEMETALATES A N D REDOX-RELATED COMPLEXES 504
14.3 C O O R D I N A T I O N A N D SURFACE C H E M I S T R Y O F N O N B
E N Z E N O I D
ISOCYANOARENES 508 14.3.1 ISOCYANOAZULENES 508
14.3.2 ORGANOMETALLIC R| 5-ISOCYANOCYCLOPENTADIENIDES 509 14.3.3 H O M O
L E P T I C COMPLEXES O F N O N B E N Z E N O I D ISOCYANOARENES 5 1 0
14.3.4 BRIDGING N O N B E N Z E N O I D ISOCYANOARENES 514 14.3.5
SELF-ASSEMBLED MONOLAYER FILMS O F N O N B E N Z E N O I D ISOCYANO- A N
D
DIISOCYANOARENES O N G O L D SURFACES 517 14.4 CONCLUSIONS A N D OUTLOOK
521
A C K N O W L E D G M E N T S 5 2 2 REFERENCES 523
15 CARBENE COMPLEXES DERIVED FROM METAL-BOUND ISOCYANIDES:
RECENT ADVANCES 5 3 1 KONSTANTIN V. LUZYANIN AND ARMANDO J. L. POMBEIRO
15.1 INTRODUCTION 531
15.2 C O U P L I N G O F T H E ISOCYANIDE LIGAND W I T H SIMPLE A M I N
E S O R
ALCOHOLS 5 3 2
15.3 C O U P L I N G O F T H E ISOCYANIDE LIGAND W I T H FUNCTIONALIZED
A M I N E S O R
ALCOHOLS 537
15.4 C O U P L I N G O F T H E ISOCYANIDE LIGAND W I T H A H Y D R A Z I
N E O R
H Y D R A Z O N E 5 3 7
15.5 COUPLING O F T H E ISOCYANIDE LIGAND W I T H A N I M I N E O R A M
I D I N E 538
15.6 INTRAMOLECULAR CYCLIZATIONS O F FUNCTIONALIZED ISOCYANIDE
LIGANDS 5 4 0
15.7 COUPLING O F ISOCYANIDES W I T H DIPOLES 543
15.8 O T H E R REACTIONS 544
15.9 FINAL R E M A R K S 5 4 6
ACKNOWLEDGMENTS 546 REFERENCES 5 4 7
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X I I | C O N T E N T S
16 POLYISOCYANIDES 551
NIELS AKEROYD, ROELANDJ. M. NOLTE, AND ALAN E. ROWAN 16.1 I N T R O D U
C T I O N 551
16.1.1 CHIRAL POLYMERS 551
16.1.2 POLYISOCYANIDES A N D T H E I R M O N O M E R S 5 5 3
16.2 T H E POLYMERIZATION M E C H A N I S M 553
16.3 C O N F O R M A T I O N O F T H E POLYMERIC BACKBONE 5 5 6
16.4 POLYISOCYANOPEPTIDES 561
16.5 POLYISOCYANIDES AS SCAFFOLDS FOR T H E A N C H O R I N G O F C H R
O M O P H O R I C MOLECULES 5 6 3
16.6 FUNCTIONAL POLYISOCYANIDES 5 7 0
16.7 CONCLUSIONS A N D O U T L O O K 5 7 5
REFERENCES 5 7 6
INDEX 5 8 7 |
| any_adam_object | 1 |
| author2 | Nenajdenko, Valentin G. |
| author2_role | edt |
| author2_variant | v g n vg vgn |
| author_GND | (DE-588)102460022X |
| author_facet | Nenajdenko, Valentin G. |
| building | Verbundindex |
| bvnumber | BV040365538 |
| classification_rvk | VK 7400 |
| ctrlnum | (OCoLC)805588364 (DE-599)DNB1019094532 |
| dewey-full | 547.044 |
| dewey-hundreds | 500 - Natural sciences and mathematics |
| dewey-ones | 547 - Organic chemistry |
| dewey-raw | 547.044 |
| dewey-search | 547.044 |
| dewey-sort | 3547.044 |
| dewey-tens | 540 - Chemistry and allied sciences |
| discipline | Chemie / Pharmazie Maschinenbau / Maschinenwesen |
| format | Book |
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| id | DE-604.BV040365538 |
| illustrated | Illustrated |
| indexdate | 2024-08-21T00:05:49Z |
| institution | BVB |
| isbn | 9783527330430 3527330437 9783527652563 9783527652556 9783527652549 9783527652532 |
| language | English |
| oai_aleph_id | oai:aleph.bib-bvb.de:BVB01-025219267 |
| oclc_num | 805588364 |
| open_access_boolean | |
| owner | DE-11 DE-29T DE-92 DE-19 DE-BY-UBM |
| owner_facet | DE-11 DE-29T DE-92 DE-19 DE-BY-UBM |
| physical | XVIII, 605 S. Ill., graph. Darst. 25 cm |
| publishDate | 2012 |
| publishDateSearch | 2012 |
| publishDateSort | 2012 |
| publisher | Wiley-VCH |
| record_format | marc |
| spelling | Isocyanide chemistry applications in synthesis and material science ed. by Valentine Nenajdenko Weinheim Wiley-VCH 2012 XVIII, 605 S. Ill., graph. Darst. 25 cm txt rdacontent n rdamedia nc rdacarrier Literaturangaben Isocyanide (DE-588)4162494-4 gnd rswk-swf Isocyanide (DE-588)4162494-4 s DE-604 Nenajdenko, Valentin G. (DE-588)102460022X edt X:MVB text/html http://deposit.dnb.de/cgi-bin/dokserv?id=3965886&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=025219267&sequence=000001&line_number=0001&func_code=DB_RECORDS&service_type=MEDIA Inhaltsverzeichnis |
| spellingShingle | Isocyanide chemistry applications in synthesis and material science Isocyanide (DE-588)4162494-4 gnd |
| subject_GND | (DE-588)4162494-4 |
| title | Isocyanide chemistry applications in synthesis and material science |
| title_auth | Isocyanide chemistry applications in synthesis and material science |
| title_exact_search | Isocyanide chemistry applications in synthesis and material science |
| title_full | Isocyanide chemistry applications in synthesis and material science ed. by Valentine Nenajdenko |
| title_fullStr | Isocyanide chemistry applications in synthesis and material science ed. by Valentine Nenajdenko |
| title_full_unstemmed | Isocyanide chemistry applications in synthesis and material science ed. by Valentine Nenajdenko |
| title_short | Isocyanide chemistry |
| title_sort | isocyanide chemistry applications in synthesis and material science |
| title_sub | applications in synthesis and material science |
| topic | Isocyanide (DE-588)4162494-4 gnd |
| topic_facet | Isocyanide |
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