Jump to main content
Jump to site search

Issue 17, 2017
Previous Article Next Article

A method for accessing sulfanylfurans from homopropargylic alcohols and sulfonyl hydrazides

Author affiliations

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

Back to tab navigation

Supplementary files

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., 2017,15, 3571-3574
  •   Request permissions

    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

Search articles by author

Spotlight

Advertisements