A new bromo trienyne: synthesis of all-E, conjugated tetra-, penta-, and hexaenes common to oxo polyene macrolide antibiotics

BH Lipshutz, B Ullman, C Lindsley…

Index: Lipshutz; Ullman; Lindsley; Pecchi; Buzard; Dickson Journal of Organic Chemistry, 1998 , vol. 63, # 18 p. 6092 - 6093

Full Text: HTML

Citation Number: 42

Abstract

In a recent report from these laboratories, 1 a new “linchpin” 1 was disclosed that allows for rapid construction of the all-E oxopolyene network characteristic of many polyene macrolide antifungal agents (Figure 1). 2 This methodology relies on an initial Pd (0) coupling, where 1 serves as the nucleophilic partner. The acetylenic terminus can be regioand stereoselectively hydrozirconated, and while introduction of an acyl moiety could be ...

Related Articles:

Stereoselective total synthesis of ieodomycin C

[Tungen, Jorn E.; Aursnes, Marius; Hansen, Trond Vidar Tetrahedron, 2014 , vol. 70, # 24 p. 3793 - 3797]

Simple and Convenient Method for the Synthesis of 2-Substituted Glutaconaldehyde Salts and 2-Substituted Glutaconaldehyde Derivatives

[Nguyen, Tuan Minh; Peixoto, Sabrina; Ouairy, Cecile; Nguyen, Tung Dinh; Benechie, Michel; Marazano, Christian; Michel, Patrick Synthesis, 2010 , # 1 p. 103 - 109]

More Articles...