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Synthesis of aplysiatoxin: stereoselective synthesis of key fragments

Authors
Journal
Tetrahedron Letters
0040-4039
Publisher
Elsevier
Publication Date
Volume
32
Issue
38
Identifiers
DOI: 10.1016/s0040-4039(00)93448-8

Abstract

Abstract Stereoselective synthesis of key fragments for the synthesis of aplysiatoxin has been achieved. All the stereogenic carbons contained in fragments B≈E were elaborated on the basis of [2,3] Wittig rearrangement and titanium-mediated asymmetric epoxidation.

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