Asymmetric Synthetic Methodology

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A01=David John Ager
A01=Michael B. East
advanced organic chemistry
Aldol Reaction
Alkyl Halide
Allyl Alcohol
Asymmetric Induction
asymmetric methodology
asymmetric synthesis techniques for researchers
Author_David John Ager
Author_Michael B. East
biochemical
biological systems
Carbon Carbon Unsaturation
Carbonyl Compounds
Carbonyl Group
Carboxylic Acid Derivatives
Category=PNN
Chiral Auxiliary
Chiral Ligand
Double Asymmetric Induction
enantioselective synthesis
Enol Ether
enzyme catalyzed transformations
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Face Selectivity
Grignard Reagent
Kinetic Resolution
Lithium Aluminum Hydride
Lithium Enolates
organic reaction mechanisms
organic synthetic methodologies
Organometallic Reagents
Peroxy Acid
Silyl Enol Ethers
Silyl Group
Simple Alkene
Stereochemical Outcome
Stereogenic Centers
stereoselective reactions
transition metal catalysis
Vide Infra

Product details

  • ISBN 9780849389429
  • Weight: 1090g
  • Dimensions: 178 x 254mm
  • Publication Date: 21 Nov 1995
  • Publisher: Taylor & Francis Inc
  • Publication City/Country: US
  • Product Form: Hardback
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This comprehensive text presents a critical discussion of the scopes and limitations of various organic synthetic methodologies that are available for performing asymmetric transformations. In addition to purely chemical methods, the book covers applications of new enzymes and other biological systems that are increasingly useful in asymmetric methodology.
David John Ager and Michael B. East

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