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ChemInform Abstract: Regioselective and Stereoselective Entry to β,β-Disubstituted Vinyl Ethers via the Sequential Hydroboration/Suzuki—Miyaura Coupling of Ynol Ethers.

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First Author : Weijian Cui

Date of Publication : 2014-01-01

Journal : ChemInform

Affiliation of Author(s) : 化学与生命科学学院

Document Type : 期刊

Volume : Vol.45

Issue : No.9

ISSN : 1522-2667

Key Words : phenol;ethers;araliphatic;ethers;C-C;bond;formation;catalysis,;phase-transfer;catalysis

Abstract : This method uses a readily available catalytic system, has a broad substrate scope, and gives the title compounds in good yields with excellent stereo- and regioselectivity.

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Pre One : ChemInform Abstract: Synthesis of cis-1,2-Dichlorovinylsulfones via Fe-Catalyzed Regio- and Stereoselective Addition of Sulfonyl Chlorides to Aromatic Chloroalkynes.

Next One : ChemInform Abstract: Synthesis of (Z)-1-Thio- and (Z)-2-Thio-1-alkenyl Boronates via Copper-Catalyzed Regiodivergent Hydroboration of Thioacetylenes: An Experimental and Theoretical Study.

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