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Stereoselective Access to Highly Substituted Vinyl Ethers via <i>trans</i> -Difunctionalization of Alkynes with Alcohols and Iodine(III) Electrophile

Wei Ding, Jinkui Chai, Chen Wang, Junliang Wu, Naohiko Yoshikai

2020Journal of the American Chemical Society93 citationsDOI

Abstract

-iodanyl vinyl ethers in good yields with high regio- and stereoselectivities. The benziodoxole moiety of the products can be used as a versatile linchpin for the synthesis of structurally diverse vinyl ethers that are difficult to access by other means.

Topics & Concepts

ChemistryElectrophileStereoselectivityMoietyTrifluoromethanesulfonateOrganic chemistryIodineCombinatorial chemistryCatalysisOxidative Organic Chemistry ReactionsCatalytic C–H Functionalization MethodsVanadium and Halogenation Chemistry
Stereoselective Access to Highly Substituted Vinyl Ethers via <i>trans</i> -Difunctionalization of Alkynes with Alcohols and Iodine(III) Electrophile | Litcius