2010/8Science of Synthesis: Stereoselective Synthesis Vol. 2

Stereoselective Reactions of Carbonyl and Imino Groups

Inbunden, Engelska, 2010

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Carbonyl and imino groups are two of the most integral functional groups employed in organic synthesis. Specific topics discussed: reduction, alkylation, alkenylation, and arylation of these groups, as well as asymmetric aldol, Mannich, and Morita-Bayliss-Hillman reactions.This volume is part of a 3-volume set: Science of Synthesis Stereoselective Synthesis Workbench EditionFurther information about Stereoselective Synthesis (including sample pages and the table of contents)

Produktinformation

Utgivningsdatum2010-11-24
Mått170 x 240 x undefined mm
Vikt454 g
FormatInbunden
SpråkEngelska
SerieScience of Synthesis
Antal sidor1 052
FörlagThieme Publishing Group
ISBN9783131541215

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Organisk kemi inom Naturvetenskap och teknik

2.1 Reduction of Carbonyl Groups: Hydrogenation2.2 Reduction of Carbonyl Groups: Transfer Hydrogenation, Hydrosilylation, Catalytic Hydroboration, and Reduction with Borohydrides, Aluminum Hydrides, or Boranes2.3 Enzymatic Reduction of Carbonyl Groups2.4 Oxidative Deracemization2.5 Stereoselective Reduction of Imino Groups2.6 Epoxidation and Aziridination of Carbonyl Groups and Imines2.7 Alkylation of Carbonyl and Imino Groups2.8 Allylation of Carbonyl and Imino Groups2.9 Arylation and Alkenylation of Carbonyl and Imino Groups2.10.1 Enantioselective Addition of Acetylide Nucleophiles to Carbonyl Compounds2.10.2 Enantioselective Addition of Metal Alkynylides to Imino Groups2.11 Hydrocyanation, Cyanosilylation, and Hydrophosphonylation of Carbonyl and Imino Groups2.12 Asymmetric Mukaiyama Aldol Reaction2.13 Direct Aldol Reactions2.14 Enzymatic Direct Aldol Additions2.15 Asymmetric Morita–Baylis–Hillman Reaction and Its Aza Analogue2.16 Mannich Reaction2.17 Asymmetric Benzoin and Stetter Reactions2.18 Asymmetric Synthesis of Spiroketals, Bisspiroketals, and Spiroaminals