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Synthesis 2014; 46(09): 1205-1210
DOI: 10.1055/s-0033-1340866
DOI: 10.1055/s-0033-1340866
paper
Total Synthesis of Aculeatins A, B and D and 6-epi-Aculeatin D via an Asymmetric Aldol Approach[1]
Further Information
Publication History
Received: 23 November 2013
Accepted after revision: 05 February 2014
Publication Date:
19 March 2014 (online)
Abstract
Simple and efficient stereoselective total syntheses of aculeatins A, B and D and 6-epi-aculeatin D starting from 1-tetradecanal have been accomplished. The synthesis is based on the Crimmins aldol reaction involving a chiral auxiliary.
Key words
aculeatins - stereoselective total synthesis - Crimmins aldol reaction - chiral auxiliary - spirocyclizationSupporting Information
- for this article is available online at http://www.thieme-connect.com/ejournals/toc/synthesis.
- Supporting Information
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