Chemistry–A European Journal

A unified strategy for the stereospecific construction of propionates and acetate–propionates relying on a directed allylic substitution

T Reiss, B Breit

Index: Reiss, Tomislav; Breit, Bernhard Chemistry - A European Journal, 2009 , vol. 15, # 26 p. 6345 - 6348

Full Text: HTML

Citation Number: 29

Abstract

Abstract Flexible friends: A new strategy that relies on o-DPPB-directed allylic substitution has been implemented for the flexible and stereospecific construction of major polyketide and isoprenoid structural elements (see scheme; o-DPPB= ortho-diphenylphosphanyl benzoate; PG= protecting group).

Related Articles:

Enantioselective transesterification of 2-methyl-1, 3-propanediol derivatives catalyzed by Pseudomonas fluorescens lipase in an organic solvent

[Grisenti; Ferraboschi; Manzocchi; Santaniello Tetrahedron, 1992 , vol. 48, # 18 p. 3827 - 3834]

Enantioselective transesterification of 2-methyl-1, 3-propanediol derivatives catalyzed by Pseudomonas fluorescens lipase in an organic solvent

[Grisenti; Ferraboschi; Manzocchi; Santaniello Tetrahedron, 1992 , vol. 48, # 18 p. 3827 - 3834]

Diisobutylaluminum hydride reductions revitalized: A fast, robust, and selective continuous flow system for aldehyde synthesis

[Webb, Damien; Jamison, Timothy F. Organic Letters, 2012 , vol. 14, # 2 p. 568 - 571]

… Compounds, XXXVIII. Ring Enlargement of Cyclodecanone by a Chiral Building Block: Synthesis and Olfactory Properties of (12R)??(+)??12??Methyl??13??Tridecanolide

[Kraft, Philip; Tochtermann, Werner Liebigs Annalen der Chemie, 1994 , # 12 p. 1161 - 1164]

Diastereoselective and Enantioselective Silylation of 2-Arylcyclohexanols

[Giustra, Zachary X.; Tan, Kian L. Chemical Communications, 2013 , vol. 49, # 39 p. 4370 - 4372]

More Articles...