Organic Syntheses Based on Name Reactions

By

  • Alfred Hassner, Department of Chemistry, Bar-Ilan University, Israel
  • C Stumer, Department of Chemistry Bar-Ilan University Ramat-Gan Israel

Since the publication of Organic Syntheses Based on Name Reactions and Unnamed Reactions, as Volume 11 in the Tetrahedron Organic Chemistry series, there has been a proliferation of newly discovered Name Reactions in the field of organic chemistry. Hence, this, the second edition of this title has focused on the ongoing development in this area of research. The revised title, Organic Syntheses Based on Name Reactions, reflects the notion whereby many new reagents and reactions are now being referred to by their names. The inclusion of over 155 new stereoselective and regioselective reagents or reactions including asymmetric syntheses, brings the total to over 540. Features that will be invaluable to the reader include over 3000 references, a names index, reagent index, reaction index and a functional group transformation index. The latter of these indexes will allow the reader to search for conversions of one functional group to another and has proved a much utilized tool for the synthetic chemist, searching for pathways to perform synthetic procedures.
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Book information

  • Published: July 2002
  • Imprint: PERGAMON
  • ISBN: 978-0-08-043259-5


Table of Contents

Name reactions. Names index. Reagents index. Reactions index. Functional group transformations index.

Examples:

Appel, Halogenation Reagent

Bailey, Crisscross Cycloaddition

Barluenga, Iodination

Barton-McCrombie, Deoxygenation

Bergman, Cycloaromatization

Brandi-Guarna, Rearrangement

Buchwald, Heterocyclization

Chiatgilialoglu, Reducing Agent

G. Enders, Heterocycle Synthesis

Grubbs, Olefin Metathesis

Jacobsen, Asymmetric Epoxidation

Kagan-Modena, Asymemetric Oxidation

Katritzky, Amine Displacement

Kawase, N-Acyl Rearrangement

Knochel, Zinc Vinyl Coupling

Kulinkovich, Hydroxycyclopropanation

Nicolaou, Oxidations

O'Donnell, Aminoacid Synthesis

Saegusa, Enone Synthesis

Shibasaki, Catalytic Nitrogenation

Yamamoto, Chiral Transfer