Verfügbarkeit: Organic chemistry: 100 must-know mechanisms

Organic chemistry: 100 must-know mechanisms:

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Bibliographische Detailangaben
1. Verfasser:	Valiulin, Roman A. (VerfasserIn)
Format:	Buch
Sprache:	English
Veröffentlicht:	Berlin ; Boston De Gruyter [2023]
Ausgabe:	2nd edition
Schriftenreihe:	De Gruyter graduate
Schlagworte:	Reaktionsmechanismus Organische Chemie Kinetik Organic Chernistry Organic Synthesis Organische Synthese Reaction Mechanisms TB: Textbook
Online-Zugang:	https://www.degruyter.com/isbn/9783110786828 Inhaltsverzeichnis
Beschreibung:	XXII, 267 Seiten Illustrationen, Diagramme
ISBN:	9783110786828 3110786826

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MARC


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Datensatz im Suchindex

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adam_text	CONTENTS SECOND EDITION - VII PREFACE AND OVERVIEW - IX LIST OF ACRONYMS AND ABBREVIATIONS - XIX 1 ELECTROPHILIC ADDITION MECHANISM - 2 2 NUCLEOPHILIC SUBSTITUTION MECHANISM - 4 3 AROMATIC ELECTROPHILIC SUBSTITUTION MECHANISM - 6 4 AROMATIC NUCLEOPHILIC SUBSTITUTION MECHANISM - 10 5 AROMATIC RADICAL NUCLEOPHILIC SUBSTITUTION MECHANISM - 12 6 ELIMINATION MECHANISM - 16 7 ACYLOIN CONDENSATION - 20 8 ALKYNE ZIPPER REACTION - 24 9 ARBUZOV REACTION - 26 10 ARNDT-EISTERT SYNTHESIS - 28 11 BAEYER-VILLIGER OXIDATION - 32 12 BARTON DECARBOXYLATION - 34 13 BAYLIS-HILLMAN REACTION - 36 14 BECKMANN REARRANGEMENT - 38 15 BENZOIN CONDENSATION - 40 16 BENZYNE MECHANISM - 42 17 BERGMAN CYCLIZATION - 44 XIV - - CONTENTS 18 19 20 21 22 23 24 25 26 27 28 29 30 31 32 33 34 35 36 37 38 BIRCH REDUCTION - 46 BISCHLER-NAPIERALSKI CYCLIZATION - 48 BROWN HYDROBORATION - 50 BUCHWALD-HARTWIG CROSS-COUPLING - 52 CANNIZZARO REACTION - 54 CHAN-EVANS-LAM CROSS-COUPLING - 56 CHICHIBABIN AMINATION - 58 CLAISEN CONDENSATION - 60 CLAISEN REARRANGEMENT - 62 COPE ELIMINATION - 64 COPE REARRANGEMENT - 66 CRIEGEE AND MALAPRADE OXIDATION - 70 CUAAC - 72 CURTIUS REARRANGEMENT - 74 DARZENS CONDENSATION - 78 DESS-MARTIN OXIDATION - 80 DIAZOTIZATION (DIAZONIUM SALT) - 82 DIELS-ALDER CYCLOADDITION - 84 DI-N-METHANE REARRANGEMENT - 90 FAVORSKII REARRANGEMENT - 92 FISCHER INDOLE SYNTHESIS - 96 CONTENTS - XV 39 40 41 42 43 44 45 46 47 48 49 50 51 52 53 54 55 56 57 58 59 FRIEDEL-CRAFTS ACYLATION AND ALKYLATION - 98 GABRIEL SYNTHESIS - 102 GEWALD REACTION - 104 GLASER-EGLINTON-HAY COUPLING - 106 GRIGNARD REACTION - 108 GROB FRAGMENTATION - 110 HALOFORM REACTION - 112 HECK CROSS-COUPLING - 114 HELL-VOLHARD-ZELINSKY REACTION - 116 HIYAMA CROSS-COUPLING - 118 HOFMANN ELIMINATION - 120 HORNER-WADSWORTH-EMMONS OLEFINATION - 122 JONES OXIDATION - 126 KUCHEROV REACTION - 128 KUMADA CROSS-COUPLING - 130 LEY-GRIFFITH OXIDATION - 132 LIEBESKIND-SROGI CROSS-COUPLING - 134 MANNICH REACTION - 136 MCMURRY COUPLING - 140 MEERWEIN-PONNDORF-VERLEY REDUCTION - 142 MICHAEL ADDITION - 144 XVI - CONTENTS 60 61 62 63 64 65 66 67 68 69 70 71 72 73 74 75 76 77 78 79 80 MINISCI REACTION - 148 MITSUNOBU REACTION - 150 MIYAURA BORYLATION - 154 MUKAIYAMA REDOX HYDRATION - 156 NAZAROV CYCLIZATION - 158 NEF REACTION -----160 NEGISHI CROSS-COUPLING - 162 NORRISH TYPE I AND II REACTIONS - 164 OLEFIN (ALKENE) METATHESIS - 166 OPPENAUER OXIDATION - 170 OZONOLYSIS - 172 PAAL-KNORR SYNTHESES - 176 PATERND-BIICHI REACTION - 180 PAUSON-KHAND REACTION - 182 PEPTIDE (AMIDE) COUPLING - 184 PICTET-SPENGLER REACTION - 188 PINACOL-PINACOLONE REARRANGEMENT - 192 POLONOVSKI REACTION - 194 PRILEZHAEV EPOXIDATION - 196 PRINS REACTION - 198 PUMMERER REARRANGEMENT - 200 CONTENTS - XVII 81 82 83 84 85 86 87 88 89 90 91 92 93 94 95 96 97 98 99 RAMBERG-BACKLUND REARRANGEMENT - 202 REFORMATSKY REACTION - 204 ROBINSON ANNULATION - 206 SHAPIRO REACTION - 208 SONOGASHIRA CROSS-COUPLING - 210 STAUDINGER REACTION - 212 STEGLICH ESTERIFICATION - 216 STILLE CROSS-COUPLING - 218 SUZUKI CROSS-COUPLING - 220 SWERN OXIDATION - 224 UGI REACTION - 226 ULLMANN ARYL-ARYL COUPLING - 228 UPJOHN DIHYDROXYLATION - 232 VILSMEIER-HAACK REACTION - 234 WACKER OXIDATION - 236 WAGNER-MEERWEIN REARRANGEMENT - 238 WEINREB KETONE SYNTHESIS - 242 WITTIG REACTION - 244 WOHL-ZIEGLER REACTION - 246 XVIII - CONTENTS 100 WOLFF-KISHNER REDUCTION - 248 ACKNOWLEDGMENTS - 251 BIBLIOGRAPHY AND REFERENCES - 253
adam_txt	CONTENTS SECOND EDITION - VII PREFACE AND OVERVIEW - IX LIST OF ACRONYMS AND ABBREVIATIONS - XIX 1 ELECTROPHILIC ADDITION MECHANISM - 2 2 NUCLEOPHILIC SUBSTITUTION MECHANISM - 4 3 AROMATIC ELECTROPHILIC SUBSTITUTION MECHANISM - 6 4 AROMATIC NUCLEOPHILIC SUBSTITUTION MECHANISM - 10 5 AROMATIC RADICAL NUCLEOPHILIC SUBSTITUTION MECHANISM - 12 6 ELIMINATION MECHANISM - 16 7 ACYLOIN CONDENSATION - 20 8 ALKYNE ZIPPER REACTION - 24 9 ARBUZOV REACTION - 26 10 ARNDT-EISTERT SYNTHESIS - 28 11 BAEYER-VILLIGER OXIDATION - 32 12 BARTON DECARBOXYLATION - 34 13 BAYLIS-HILLMAN REACTION - 36 14 BECKMANN REARRANGEMENT - 38 15 BENZOIN CONDENSATION - 40 16 BENZYNE MECHANISM - 42 17 BERGMAN CYCLIZATION - 44 XIV - - CONTENTS 18 19 20 21 22 23 24 25 26 27 28 29 30 31 32 33 34 35 36 37 38 BIRCH REDUCTION - 46 BISCHLER-NAPIERALSKI CYCLIZATION - 48 BROWN HYDROBORATION - 50 BUCHWALD-HARTWIG CROSS-COUPLING - 52 CANNIZZARO REACTION - 54 CHAN-EVANS-LAM CROSS-COUPLING - 56 CHICHIBABIN AMINATION - 58 CLAISEN CONDENSATION - 60 CLAISEN REARRANGEMENT - 62 COPE ELIMINATION - 64 COPE REARRANGEMENT - 66 CRIEGEE AND MALAPRADE OXIDATION - 70 CUAAC - 72 CURTIUS REARRANGEMENT - 74 DARZENS CONDENSATION - 78 DESS-MARTIN OXIDATION - 80 DIAZOTIZATION (DIAZONIUM SALT) - 82 DIELS-ALDER CYCLOADDITION - 84 DI-N-METHANE REARRANGEMENT - 90 FAVORSKII REARRANGEMENT - 92 FISCHER INDOLE SYNTHESIS - 96 CONTENTS - XV 39 40 41 42 43 44 45 46 47 48 49 50 51 52 53 54 55 56 57 58 59 FRIEDEL-CRAFTS ACYLATION AND ALKYLATION - 98 GABRIEL SYNTHESIS - 102 GEWALD REACTION - 104 GLASER-EGLINTON-HAY COUPLING - 106 GRIGNARD REACTION - 108 GROB FRAGMENTATION - 110 HALOFORM REACTION - 112 HECK CROSS-COUPLING - 114 HELL-VOLHARD-ZELINSKY REACTION - 116 HIYAMA CROSS-COUPLING - 118 HOFMANN ELIMINATION - 120 HORNER-WADSWORTH-EMMONS OLEFINATION - 122 JONES OXIDATION - 126 KUCHEROV REACTION - 128 KUMADA CROSS-COUPLING - 130 LEY-GRIFFITH OXIDATION - 132 LIEBESKIND-SROGI CROSS-COUPLING - 134 MANNICH REACTION - 136 MCMURRY COUPLING - 140 MEERWEIN-PONNDORF-VERLEY REDUCTION - 142 MICHAEL ADDITION - 144 XVI - CONTENTS 60 61 62 63 64 65 66 67 68 69 70 71 72 73 74 75 76 77 78 79 80 MINISCI REACTION - 148 MITSUNOBU REACTION - 150 MIYAURA BORYLATION - 154 MUKAIYAMA REDOX HYDRATION - 156 NAZAROV CYCLIZATION - 158 NEF REACTION -----160 NEGISHI CROSS-COUPLING - 162 NORRISH TYPE I AND II REACTIONS - 164 OLEFIN (ALKENE) METATHESIS - 166 OPPENAUER OXIDATION - 170 OZONOLYSIS - 172 PAAL-KNORR SYNTHESES - 176 PATERND-BIICHI REACTION - 180 PAUSON-KHAND REACTION - 182 PEPTIDE (AMIDE) COUPLING - 184 PICTET-SPENGLER REACTION - 188 PINACOL-PINACOLONE REARRANGEMENT - 192 POLONOVSKI REACTION - 194 PRILEZHAEV EPOXIDATION - 196 PRINS REACTION - 198 PUMMERER REARRANGEMENT - 200 CONTENTS - XVII 81 82 83 84 85 86 87 88 89 90 91 92 93 94 95 96 97 98 99 RAMBERG-BACKLUND REARRANGEMENT - 202 REFORMATSKY REACTION - 204 ROBINSON ANNULATION - 206 SHAPIRO REACTION - 208 SONOGASHIRA CROSS-COUPLING - 210 STAUDINGER REACTION - 212 STEGLICH ESTERIFICATION - 216 STILLE CROSS-COUPLING - 218 SUZUKI CROSS-COUPLING - 220 SWERN OXIDATION - 224 UGI REACTION - 226 ULLMANN ARYL-ARYL COUPLING - 228 UPJOHN DIHYDROXYLATION - 232 VILSMEIER-HAACK REACTION - 234 WACKER OXIDATION - 236 WAGNER-MEERWEIN REARRANGEMENT - 238 WEINREB KETONE SYNTHESIS - 242 WITTIG REACTION - 244 WOHL-ZIEGLER REACTION - 246 XVIII - CONTENTS 100 WOLFF-KISHNER REDUCTION - 248 ACKNOWLEDGMENTS - 251 BIBLIOGRAPHY AND REFERENCES - 253
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author	Valiulin, Roman A.
author_GND	(DE-588)1197817336
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ctrlnum	(OCoLC)1405908689 (DE-599)DNB1284094820
discipline	Chemie / Pharmazie Chemie
discipline_str_mv	Chemie / Pharmazie Chemie
edition	2nd edition
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spelling	Valiulin, Roman A. Verfasser (DE-588)1197817336 aut Organic chemistry: 100 must-know mechanisms Roman A. Valiulin 2nd edition Berlin ; Boston De Gruyter [2023] © 2023 XXII, 267 Seiten Illustrationen, Diagramme txt rdacontent n rdamedia nc rdacarrier De Gruyter graduate Reaktionsmechanismus (DE-588)4177123-0 gnd rswk-swf Organische Chemie (DE-588)4043793-0 gnd rswk-swf Kinetik Organic Chernistry Organic Synthesis Organische Chemie Organische Synthese Reaction Mechanisms Reaktionsmechanismus TB: Textbook Organische Chemie (DE-588)4043793-0 s Reaktionsmechanismus (DE-588)4177123-0 s DE-604 Walter de Gruyter GmbH & Co. KG (DE-588)10095502-2 pbl Erscheint auch als Online-Ausgabe, PDF 978-3-11-078683-5 Erscheint auch als Online-Ausgabe, EPUB 978-3-11-078701-6 Vorangegangen ist 978-3-11-060830-4 X:MVB https://www.degruyter.com/isbn/9783110786828 DNB Datenaustausch application/pdf http://bvbr.bib-bvb.de:8991/F?func=service&doc_library=BVB01&local_base=BVB01&doc_number=034310303&sequence=000001&line_number=0001&func_code=DB_RECORDS&service_type=MEDIA Inhaltsverzeichnis
spellingShingle	Valiulin, Roman A. Organic chemistry: 100 must-know mechanisms Reaktionsmechanismus (DE-588)4177123-0 gnd Organische Chemie (DE-588)4043793-0 gnd
subject_GND	(DE-588)4177123-0 (DE-588)4043793-0
title	Organic chemistry: 100 must-know mechanisms
title_auth	Organic chemistry: 100 must-know mechanisms
title_exact_search	Organic chemistry: 100 must-know mechanisms
title_exact_search_txtP	Organic chemistry: 100 must-know mechanisms
title_full	Organic chemistry: 100 must-know mechanisms Roman A. Valiulin
title_fullStr	Organic chemistry: 100 must-know mechanisms Roman A. Valiulin
title_full_unstemmed	Organic chemistry: 100 must-know mechanisms Roman A. Valiulin
title_short	Organic chemistry: 100 must-know mechanisms
title_sort	organic chemistry 100 must know mechanisms
topic	Reaktionsmechanismus (DE-588)4177123-0 gnd Organische Chemie (DE-588)4043793-0 gnd
topic_facet	Reaktionsmechanismus Organische Chemie
url	https://www.degruyter.com/isbn/9783110786828 http://bvbr.bib-bvb.de:8991/F?func=service&doc_library=BVB01&local_base=BVB01&doc_number=034310303&sequence=000001&line_number=0001&func_code=DB_RECORDS&service_type=MEDIA
work_keys_str_mv	AT valiulinromana organicchemistry100mustknowmechanisms AT walterdegruytergmbhcokg organicchemistry100mustknowmechanisms

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