Issue 42, 2015

Generation of cycloheptynes and cyclooctynes via a sulfoxide–magnesium exchange reaction of readily synthesized 2-sulfinylcycloalkenyl triflates

Abstract

Cycloheptynes and cyclooctynes were efficiently generated via a sulfoxide–magnesium exchange reaction of readily synthesized 2-sulfinylcycloalkenyl triflates. Cycloadditions between various ynophiles and the cycloalkynes generated by this method proceeded efficiently, providing an easy method to prepare a wide range of heterocycles fused with seven- or eight-membered carbocycles.

Graphical abstract: Generation of cycloheptynes and cyclooctynes via a sulfoxide–magnesium exchange reaction of readily synthesized 2-sulfinylcycloalkenyl triflates

Supplementary files

Article information

Article type
Communication
Submitted
02 Mar 2015
Accepted
07 Apr 2015
First published
09 Apr 2015

Chem. Commun., 2015,51, 8745-8748

Generation of cycloheptynes and cyclooctynes via a sulfoxide–magnesium exchange reaction of readily synthesized 2-sulfinylcycloalkenyl triflates

S. Yoshida, F. Karaki, K. Uchida and T. Hosoya, Chem. Commun., 2015, 51, 8745 DOI: 10.1039/C5CC01784J

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