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A method for accessing sulfanylfurans from homopropargylic alcohols and sulfonyl hydrazides

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Abstract

A sulfenylation/cyclization reaction has been developed for the synthesis of sulfanylfurans in the presence of iodine. These processes provide facile strategies to construct C–S/O bonds, and expand the methods of synthesizing sulfanylfurans. In this transformation, various groups on homopropargylic alcohols and sulfonyl hydrazides react smoothly and the desired sulfanylfurans are obtained in moderate to good yields.

Graphical abstract: A method for accessing sulfanylfurans from homopropargylic alcohols and sulfonyl hydrazides

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Publication details

The article was received on 07 Mar 2017, accepted on 03 Apr 2017 and first published on 03 Apr 2017


Article type: Communication
DOI: 10.1039/C7OB00566K
Citation: Org. Biomol. Chem., 2017, Advance Article
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    A method for accessing sulfanylfurans from homopropargylic alcohols and sulfonyl hydrazides

    X. Yang and R. Yan, Org. Biomol. Chem., 2017, Advance Article , DOI: 10.1039/C7OB00566K

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