These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


PUBMED FOR HANDHELDS

Search MEDLINE/PubMed


  • Title: Concise total synthesis of (-)-muricatacin by tandem ring-closing/cross metathesis.
    Author: Quinn KJ, Isaacs AK, Arvary RA.
    Journal: Org Lett; 2004 Nov 11; 6(23):4143-5. PubMed ID: 15524428.
    Abstract:
    A strategy for the synthesis of chiral 5-(1-hydroxyalk-2-enyl)-5H-furan-2-ones and its application to the total synthesis of (-)-muricatacin, in four steps and 37% overall yield from (R,R)-hexa-1,5-diene-3,4-diol, are described. The key synthetic step in this approach is a highly regioselective and stereoselective tandem ring-closing/cross metathesis reaction in which both lactone formation and alkyl chain extension are accomplished in an efficient one-pot process.
    [Abstract] [Full Text] [Related] [New Search]