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: Enantioselective synthesis of beta-iodo Morita-Baylis-Hillman esters by a catalytic asymmetric three-component coupling reaction.
    Author: Senapati BK, Hwang GS, Lee S, Ryu DH.
    Journal: Angew Chem Int Ed Engl; 2009; 48(24):4398-401. PubMed ID: 19415700.
    Abstract:
    A catalytic route toward chiral Morita-Baylis-Hillman esters by asymmetric coupling between alpha,beta-acetylenic esters, aldehydes, and trimethylsilyl iodide has been developed (see scheme). The reaction proceeds with high to excellent enantioselectivities, and the products can be transformed into beta-branched derivatives in a single step and with excellent retention of configuration. TMS = trimethylsilyl.
    [Abstract] [Full Text] [Related] [New Search]