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Regioselective and stereoselective entry to beta,beta- disubstituted vinyl ethers via the sequential hydroboration/Suzuki-Miyaura coupling of ynol ethers.

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First Author : Cui W

Date of Publication : 2013-01-01

Journal : J Org Chem

Affiliation of Author(s) : 化学与生命科学学院

Document Type : 期刊

Volume : Vol.78

Issue : No.19

Abstract : A highly regio- and stereoselective synthesis of stereodefined beta,beta- disubstituted alkenyl ethers featuring the sequential hydroboration/Suzuki-Miyaura coupling of ynol ethers has been described. A number of functional groups, including OMe, Ac, CO2E

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Pre One : ChemInform Abstract: Pd-Catalyzed Addition of Boronic Acids to Ynol Ethers: A Highly Regio- and Stereoselective Synthesis of Trisubstituted Vinyl Ethers.

Next One : ChemInform Abstract: Approach to Highly Functionalized Oxazolones by a Pd-Catalyzed Cyclization of N-Alkynyl tert-Butyloxycarbamates.

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