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 [2020]
Schriftenreihe:	De Gruyter Graduate
Schlagworte:	Organische Chemie Organische Synthese Reaktionsmechanismus SCIENCE / Chemistry / Organic
Online-Zugang:	Inhaltsverzeichnis
Beschreibung:	X, 239 Seiten Illustrationen, Diagramme (teilweise farbig)
ISBN:	9783110608304

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Datensatz im Suchindex

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adam_text	CONTENTS PREFACE AND OVERVIEW - VII LIST OF ACRONYMS AND ABBREVIATIONS - 6 1 ELECTROPHILIC ADDITION MECHANISM - 10 2 NUCLEOPHILIC SUBSTITUTION MECHANISM - 12 3 AROMATIC ELECTROPHILIC SUBSTITUTION MECHANISM - 14 4 AROMATIC NUCLEOPHILIC SUBSTITUTION MECHANISM - 16 5 AROMATIC RADICAL NUCLEOPHILIC SUBSTITUTION MECHANISM - 18 6 ELIMINATION MECHANISM - 22 7 ACYLOIN CONDENSATION - 26 8 ALKYNE ZIPPER REACTION - 28 9 ARBUZOV REACTION - 30 10 ARNDT-EISTERT SYNTHESIS - 32 11 BAEYER-VILLIGER OXIDATION - 34 12 BARTON DECARBOXYLATION - 36 13 BAYLIS-HILLMAN REACTION - 38 14 BECKMANN REARRANGEMENT - 40 15 BENZOIN CONDENSATION - 42 16 BENZYNE MECHANISM - 44 17 BERGMAN CYCLIZATION - 46 18 BIRCH REDUCTION - 48 2 ---- 19 20 21 22 23 24 25 26 27 28 29 30 31 32 33 34 35 36 37 38 39 CONTENTS BISCHLER-NAPIERALSKI CYCLIZATION - 50 BROWN HYDROBORATION - 52 BUCHWALD-HARTWIG CROSS COUPLING - 54 CANNIZZARO REACTION - 56 CHAN-EVANS-LAM CROSS COUPLING - 58 CHICHIBABIN AMINATION - 60 CLAISEN CONDENSATION - 62 CLAISEN REARRANGEMENT - 64 COPE ELIMINATION - 66 COPE REARRANGEMENT - 68 CRIEGEE & 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 - 86 FAVORSKII REARRANGEMENT - 88 FISCHER INDOLE SYNTHESIS - 90 FRIEDEL-CRAFTS ACYLATION & ALKYLATION - 92 40 41 42 43 44 45 46 47 48 49 50 51 52 53 54 55 56 57 58 59 60 CONTENTS - 3 GABRIEL SYNTHESIS - 94 GEWALD REACTION - 96 GLASER-EGLINTON-HAY COUPLING - 98 GRIGNARD REACTION - 100 GROB FRAGMENTATION - 102 HALOFORM REACTION - 104 HECK CROSS COUPLING - 106 HELL-VOLHARD-ZELINSKY REACTION - 108 HIYAMA CROSS COUPLING - 110 HOFMANN ELIMINATION - 112 HORNER-WADSWORTH-EMMONS OLEFINATION - 114 JONES OXIDATION - 116 KUCHEROV REACTION - 118 KUMADA CROSS COUPLING - 120 LEY-GRIFFITH OXIDATION - 122 LIEBESKIND-SROGL CROSS COUPLING - 124 MANNICH REACTION - 126 MCMURRY COUPLING - 128 MEERWEIN-PONNDORF-VERLEY REDUCTION - 130 MICHAEL ADDITION - 132 MINISCI REACTION - 134 4 ---- 61 62 63 64 65 66 67 68 69 70 71 72 73 74 75 76 77 78 79 80 81 CONTENTS MITSUNOBU REACTION - 136 MIYAURA BORYLATION - 138 MUKAIYAMA REDOX HYDRATION - 140 NAZAROV CYCLIZATION - 142 NEF REACTION - 144 NEGLSHL CROSS COUPLING - 146 NORRISH TYPE I & II REACTION - 148 OLEFIN (ALKENE) METATHESIS - 150 OPPENAUER OXIDATION - 154 OZONOLYSIS - 156 PAAL-KNORR SYNTHESES - 158 PATERND-BLKHI REACTION - 162 PAUSON-KHAND REACTION - 164 PEPTIDE (AMIDE) COUPLING - 166 PICTET-SPENGLER REACTION - 170 PINACOL-PINACOLONE REARRANGEMENT - 172 POLONOVSKI REACTION - 174 PRILEZHAEV EPOXIDATION - 176 PRINS REACTION - 178 PUMMERER REARRANGEMENT - 180 RAMBERG-BSCKLUND REARRANGEMENT - 182 CONTENTS - 5 82 REFORMATSKY REACTION - 184 83 ROBINSON ANNULATION - 186 84 SHAPIRO REACTION - 188 85 SONOGASHLRA CROSS COUPLING - 190 86 STAUDLNGER REACTION - 192 87 STEGLICH ESTERIFICATION - 194 88 STILLE CROSS COUPLING - 196 89 SUZUKI CROSS COUPLING - 198 90 SWERN OXIDATION - 200 91 UGI REACTION - 202 92 ULLMANN ARYL-ARYL COUPLING - 204 93 UPJOHN DIHYDROXYLATION - 206 94 VILSMEIER-HAACK REACTION - 208 95 WACKER OXIDATION - 210 96 WAGNER-MEERWELN REARRANGEMENT - 212 97 WEINREB KETONE SYNTHESIS - 214 98 WITTIG REACTION - 216 99 WOHL-ZIEGLER REACTION - 218 100 WOLFF-KLSHNER REDUCTION - 220 ACKNOWLEDGMENTS - 223 BIBLIOGRAPHY AND REFERENCES - 225
adam_txt	CONTENTS PREFACE AND OVERVIEW - VII LIST OF ACRONYMS AND ABBREVIATIONS - 6 1 ELECTROPHILIC ADDITION MECHANISM - 10 2 NUCLEOPHILIC SUBSTITUTION MECHANISM - 12 3 AROMATIC ELECTROPHILIC SUBSTITUTION MECHANISM - 14 4 AROMATIC NUCLEOPHILIC SUBSTITUTION MECHANISM - 16 5 AROMATIC RADICAL NUCLEOPHILIC SUBSTITUTION MECHANISM - 18 6 ELIMINATION MECHANISM - 22 7 ACYLOIN CONDENSATION - 26 8 ALKYNE ZIPPER REACTION - 28 9 ARBUZOV REACTION - 30 10 ARNDT-EISTERT SYNTHESIS - 32 11 BAEYER-VILLIGER OXIDATION - 34 12 BARTON DECARBOXYLATION - 36 13 BAYLIS-HILLMAN REACTION - 38 14 BECKMANN REARRANGEMENT - 40 15 BENZOIN CONDENSATION - 42 16 BENZYNE MECHANISM - 44 17 BERGMAN CYCLIZATION - 46 18 BIRCH REDUCTION - 48 2 ---- 19 20 21 22 23 24 25 26 27 28 29 30 31 32 33 34 35 36 37 38 39 CONTENTS BISCHLER-NAPIERALSKI CYCLIZATION - 50 BROWN HYDROBORATION - 52 BUCHWALD-HARTWIG CROSS COUPLING - 54 CANNIZZARO REACTION - 56 CHAN-EVANS-LAM CROSS COUPLING - 58 CHICHIBABIN AMINATION - 60 CLAISEN CONDENSATION - 62 CLAISEN REARRANGEMENT - 64 COPE ELIMINATION - 66 COPE REARRANGEMENT - 68 CRIEGEE & 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 - 86 FAVORSKII REARRANGEMENT - 88 FISCHER INDOLE SYNTHESIS - 90 FRIEDEL-CRAFTS ACYLATION & ALKYLATION - 92 40 41 42 43 44 45 46 47 48 49 50 51 52 53 54 55 56 57 58 59 60 CONTENTS - 3 GABRIEL SYNTHESIS - 94 GEWALD REACTION - 96 GLASER-EGLINTON-HAY COUPLING - 98 GRIGNARD REACTION - 100 GROB FRAGMENTATION - 102 HALOFORM REACTION - 104 HECK CROSS COUPLING - 106 HELL-VOLHARD-ZELINSKY REACTION - 108 HIYAMA CROSS COUPLING - 110 HOFMANN ELIMINATION - 112 HORNER-WADSWORTH-EMMONS OLEFINATION - 114 JONES OXIDATION - 116 KUCHEROV REACTION - 118 KUMADA CROSS COUPLING - 120 LEY-GRIFFITH OXIDATION - 122 LIEBESKIND-SROGL CROSS COUPLING - 124 MANNICH REACTION - 126 MCMURRY COUPLING - 128 MEERWEIN-PONNDORF-VERLEY REDUCTION - 130 MICHAEL ADDITION - 132 MINISCI REACTION - 134 4 ---- 61 62 63 64 65 66 67 68 69 70 71 72 73 74 75 76 77 78 79 80 81 CONTENTS MITSUNOBU REACTION - 136 MIYAURA BORYLATION - 138 MUKAIYAMA REDOX HYDRATION - 140 NAZAROV CYCLIZATION - 142 NEF REACTION - 144 NEGLSHL CROSS COUPLING - 146 NORRISH TYPE I & II REACTION - 148 OLEFIN (ALKENE) METATHESIS - 150 OPPENAUER OXIDATION - 154 OZONOLYSIS - 156 PAAL-KNORR SYNTHESES - 158 PATERND-BLKHI REACTION - 162 PAUSON-KHAND REACTION - 164 PEPTIDE (AMIDE) COUPLING - 166 PICTET-SPENGLER REACTION - 170 PINACOL-PINACOLONE REARRANGEMENT - 172 POLONOVSKI REACTION - 174 PRILEZHAEV EPOXIDATION - 176 PRINS REACTION - 178 PUMMERER REARRANGEMENT - 180 RAMBERG-BSCKLUND REARRANGEMENT - 182 CONTENTS - 5 82 REFORMATSKY REACTION - 184 83 ROBINSON ANNULATION - 186 84 SHAPIRO REACTION - 188 85 SONOGASHLRA CROSS COUPLING - 190 86 STAUDLNGER REACTION - 192 87 STEGLICH ESTERIFICATION - 194 88 STILLE CROSS COUPLING - 196 89 SUZUKI CROSS COUPLING - 198 90 SWERN OXIDATION - 200 91 UGI REACTION - 202 92 ULLMANN ARYL-ARYL COUPLING - 204 93 UPJOHN DIHYDROXYLATION - 206 94 VILSMEIER-HAACK REACTION - 208 95 WACKER OXIDATION - 210 96 WAGNER-MEERWELN REARRANGEMENT - 212 97 WEINREB KETONE SYNTHESIS - 214 98 WITTIG REACTION - 216 99 WOHL-ZIEGLER REACTION - 218 100 WOLFF-KLSHNER REDUCTION - 220 ACKNOWLEDGMENTS - 223 BIBLIOGRAPHY AND REFERENCES - 225
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spelling	Valiulin, Roman A. Verfasser (DE-588)1197817336 aut Organic chemistry: 100 must-know mechanisms Roman A. Valiulin Berlin ; Boston De Gruyter [2020] © 2020 X, 239 Seiten Illustrationen, Diagramme (teilweise farbig) txt rdacontent n rdamedia nc rdacarrier De Gruyter Graduate Organische Chemie Organische Synthese Reaktionsmechanismus SCIENCE / Chemistry / Organic bisacsh Reaktionsmechanismus (DE-588)4177123-0 gnd rswk-swf Organische Chemie (DE-588)4043793-0 gnd rswk-swf Organische Chemie (DE-588)4043793-0 s Reaktionsmechanismus (DE-588)4177123-0 s DE-604 Erscheint auch als Online-Ausgabe, PDF 978-3-11-060837-3 Erscheint auch als Online-Ausgabe, EPUB 978-3-11-060851-9 DNB Datenaustausch application/pdf http://bvbr.bib-bvb.de:8991/F?func=service&doc_library=BVB01&local_base=BVB01&doc_number=032167433&sequence=000001&line_number=0001&func_code=DB_RECORDS&service_type=MEDIA Inhaltsverzeichnis
spellingShingle	Valiulin, Roman A. Organic chemistry: 100 must-know mechanisms Organische Chemie Organische Synthese Reaktionsmechanismus SCIENCE / Chemistry / Organic bisacsh 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	Organische Chemie Organische Synthese Reaktionsmechanismus SCIENCE / Chemistry / Organic bisacsh Reaktionsmechanismus (DE-588)4177123-0 gnd Organische Chemie (DE-588)4043793-0 gnd
topic_facet	Organische Chemie Organische Synthese Reaktionsmechanismus SCIENCE / Chemistry / Organic
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