Synthetic Studies Directed Toward Streptenol D: Enantioselective Preparation of the 3,5-diacetoxy-6E,8E-decadiene Segment

Authors

Bireshwar Dasgupta, Marquette University
William Donaldson, Marquette UniversityFollow

Document Type

Article

Language

eng

Publication Date

11-6-1998

Publisher

Elsevier

Source Publication

Tetrahedron: Asymmetry

Source ISSN

0957-4166

Abstract

The enantioselective preparation of 2-(3′R,5′R-diacetoxy-6E,8E-decadienyl)-1,3-dioxane, (+)-13, is described. This synthesis of the skeleton of streptenol D utilizes the ability of a diene-complexed (tricarbonyl)iron unit to serve as a protecting and stereodirecting functionality.

Comments

Accepted version. Tetrahedron: Asymmetry, Vol. 9, No. 21 (November 6, 1998): 3781-3788. DOI. © 1998 Elsevier Science Ltd. Used with permission.

Recommended Citation

Dasgupta, Bireshwar and Donaldson, William, "Synthetic Studies Directed Toward Streptenol D: Enantioselective Preparation of the 3,5-diacetoxy-6E,8E-decadiene Segment" (1998). Chemistry Faculty Research and Publications. 838.
https://epublications.marquette.edu/chem_fac/838