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

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ACETYLIDE NUCLEOPHILES
ALDOL REACTION
ALKYNYLATION
ALLYLATION
ALUMINUM HYDRIDES
ARYLATION
ASYMMETRIC BENZOIN
BISSPIROKETALS
BORANES
BOROHYDRIDES
CARBONYL GROUPS
CATALYTIC HYDROBORATION
Category=PNN
CYANOSILYLATION
ENANTIOSELECTIVE ADDITION
ENZYMATIC REDUCTION
EPOXIDATION
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HYDROCYANATION
HYDROGENATION
HYDROPHOSPHONYLATION
HYDROSILYLATION
IMINO GROUPS
MANNICH REACTION
METAL ALKYNYLIDES
MORITA-BAYLIS-HILLMAN REACTION
MUKAIYAMA ALDOL REACTION
ORGANIC CHEMISTRY
OXIDATIVE DERACEMIZATION
PEPTIDE SYNTHESIS
REACTIONS
REDUCTION
REFERENCE WORK
REVIEW
SPIROAMINALS
SPIROKETALS
STEREOSELECTIVE REDUCTION
STEREOSELECTIVE SYNTHESIS
STETTER REACTION
synthetic chemistry
SYNTHETIC TRANSFORMATION

Product details

  • ISBN 9783131541215
  • Weight: 454g
  • Dimensions: 170 x 240mm
  • Publication Date: 24 Nov 2010
  • Publisher: Thieme Publishing Group
  • Publication City/Country: DE
  • Product Form: Hardback
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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 Edition

Further information about Stereoselective Synthesis (including sample pages and the table of contents)