Efficient and highly enantioselective formation of the all-carbon quaternary stereocentre of lyngbyatoxin A

Paulo J.V. Vital, David Tanner

Research output: Contribution to journalJournal articleResearchpeer-review

Abstract

Indole 25, an advanced intermediate in a projected enantioselective total synthesis of lyngbyatoxin A 1, was prepared from allylic alcohol 11 in 9 steps and >95% ee, key transformations being the enantiospecific rearrangement of vinyl epoxide 14 and the Hemetsberger-Knittel reaction of azide 24.
Original languageEnglish
JournalOrganic & Biomolecular Chemistry
Volume4
Issue number23
Pages (from-to)4292-4298
ISSN1477-0520
DOIs
Publication statusPublished - 2006

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