Synthesis of the C14-C29 segment of amphidinolide U utilizing a tandem dihydroxylation-S(N)2 cyclization protocol

TitleSynthesis of the C14-C29 segment of amphidinolide U utilizing a tandem dihydroxylation-S(N)2 cyclization protocol
Publication TypeJournal Article
Year of Publication2008
AuthorsMohapatra, DK, Rahaman, H
JournalSynlett
Issue6
Pagination837-840
Date PublishedAPR
Type of ArticleArticle
ISSN0936-5214
Keywordsamphidinolide U, Cytotoxic, Nozaki-Hiyama-Kishi coupling, tandem dihydroxylation-S(N)2 cyclization, Wittig reaction
Abstract

The synthesis of the C14-C29 subunit of amphidinolide U is described. The key steps include the trans-2,5-disubstituted tetrahydrofurans via a highly diastereoselective and high yielding tandem dihydroxylation-S(N)2 cyclization, Wittig reaction, and Nozaki-Hiyama-Kishi coupling reaction.

DOI10.1055/s-2008-1042931
Type of Journal (Indian or Foreign)Foreign
Impact Factor (IF)2.323
Divison category: 
Organic Chemistry