Issue 17, 2017

A method for accessing sulfanylfurans from homopropargylic alcohols and sulfonyl hydrazides

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

Supplementary files

Article information

Article type
Communication
Submitted
07 Mar 2017
Accepted
03 Apr 2017
First published
03 Apr 2017

Org. Biomol. Chem., 2017,15, 3571-3574

A method for accessing sulfanylfurans from homopropargylic alcohols and sulfonyl hydrazides

X. Yang and R. Yan, Org. Biomol. Chem., 2017, 15, 3571 DOI: 10.1039/C7OB00566K

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