Author: JieJackLi
Language: English
ISBN/ISSN: 9787030211910
Published on: 2008-01
Hardcover
The third edition contains major improvements over the previous two ditions.Each reaction is now supplemented with two to three representative examples in synthesis to showcase its synthetic utility.
Abbreviations
Alder ene reaction
Aldol condensation
Algar – Flynn – Oyamada reaction
Allan-Robinson reaction
Appel reaction
Arndt-Eistert homologation
Baeyer-Villiger oxidation
Baker-Venkataraman rearrangement
Bamberger rearrangement
Bamford-Stevens reaction
Barbier coupling reaction
Bargellini reaction
Bartoli indole synthesis
Barton radical decarboxylation
Barton-McCombie deoxygenation
Barton nitrite phololysis
Barton-Zard reaction
Batcho-Leimgruber indole synthesis
Baylis-Hillman reaction
Beckmann rearrangement
Beirut reaction
Benzilic acid rearrangement
Beirut condensation
Bergman cyclization
Biginelli pyrimidone synthesis
……
Sternbach benzodiazepine synthesis
Stetter reaction
Still-Gennari phosphonate reaction
Stille coupling Stille –Kelly reaction
Stobbe condensation
Strecker amino acid synthesis
Suzuki coupling
Swern oxidation
Takai iodoalkene Synthesis
Tebbe olefination
TEMPO-mediated oxidation
Thorpe-Ziegler reaction
Tsuji-Trost allylation
Ugi reaction
Ullmann reaction
Van Leusen oxazole synthesis
Vilsmeier mechanism for acid chloride formation
Vinylcyclopropane-cyclopentene rearrangement
Von Braun recation
Wacker oxidation
Wagner-Meerwein rearrangement
Weiss-Cook reaction
Wharton oxygen transposistion reaction
Willgerodt-Kindler reaction
Wittig reaction
[1,2]-Wittig rearrangement
[2,3]-Wittig rearrangement
Wohl-Ziegler reaction
Wolff rearrangement
Wolff-Kishner reduction
Yamaguchi esterification
Zincke reaction
Subject Index
Language: English
ISBN/ISSN: 9787030211910
Published on: 2008-01
Hardcover
The third edition contains major improvements over the previous two ditions.Each reaction is now supplemented with two to three representative examples in synthesis to showcase its synthetic utility.
Abbreviations
Alder ene reaction
Aldol condensation
Algar – Flynn – Oyamada reaction
Allan-Robinson reaction
Appel reaction
Arndt-Eistert homologation
Baeyer-Villiger oxidation
Baker-Venkataraman rearrangement
Bamberger rearrangement
Bamford-Stevens reaction
Barbier coupling reaction
Bargellini reaction
Bartoli indole synthesis
Barton radical decarboxylation
Barton-McCombie deoxygenation
Barton nitrite phololysis
Barton-Zard reaction
Batcho-Leimgruber indole synthesis
Baylis-Hillman reaction
Beckmann rearrangement
Beirut reaction
Benzilic acid rearrangement
Beirut condensation
Bergman cyclization
Biginelli pyrimidone synthesis
……
Sternbach benzodiazepine synthesis
Stetter reaction
Still-Gennari phosphonate reaction
Stille coupling Stille –Kelly reaction
Stobbe condensation
Strecker amino acid synthesis
Suzuki coupling
Swern oxidation
Takai iodoalkene Synthesis
Tebbe olefination
TEMPO-mediated oxidation
Thorpe-Ziegler reaction
Tsuji-Trost allylation
Ugi reaction
Ullmann reaction
Van Leusen oxazole synthesis
Vilsmeier mechanism for acid chloride formation
Vinylcyclopropane-cyclopentene rearrangement
Von Braun recation
Wacker oxidation
Wagner-Meerwein rearrangement
Weiss-Cook reaction
Wharton oxygen transposistion reaction
Willgerodt-Kindler reaction
Wittig reaction
[1,2]-Wittig rearrangement
[2,3]-Wittig rearrangement
Wohl-Ziegler reaction
Wolff rearrangement
Wolff-Kishner reduction
Yamaguchi esterification
Zincke reaction
Subject Index