Biomimetic Synthesis toward the Transtaganolides/Basiliolides.

Rikard Larsson, Olov Sterner, Martin H Johansson

Research output: Contribution to journalArticlepeer-review

Abstract

A concise biomimetic approach toward transtaganolides C and D involving an Ireland-Claisen rearrangement/intramolecular Diels-Alder reaction sequence suggesting the involvement of pericyclic reactions in the biosynthesis of these biologically active plant metabolites is presented. A final coupling reaction establishes the carbon framework of the transtaganolides.
Original languageEnglish
Pages (from-to)657-660
JournalOrganic Letters
Volume11
Issue number3
DOIs
Publication statusPublished - 2009

Bibliographical note

The information about affiliations in this record was updated in December 2015.
The record was previously connected to the following departments: Organic chemistry (S/LTH) (011001240)

Subject classification (UKÄ)

  • Organic Chemistry

Fingerprint

Dive into the research topics of 'Biomimetic Synthesis toward the Transtaganolides/Basiliolides.'. Together they form a unique fingerprint.

Cite this