作者:Vladimir A. Ogurtsov、Oleg A. Rakitin、Charles W. Rees、Alexey A. Smolentsev
DOI:10.1070/mc2005v015n02abeh002086
日期:2005.1
The thiocarbonyl group of 4,5-dichloro-1,2-dithiole-3-thione reacts as a 1,3-dipolarophile towards diaryl nitrile imines by 1,3-dipolar cycloaddition followed by opening of the dithiole ring with loss of sulfur to give 5-methylene-1,3,4-thiadiazolines; this reaction together with nucleophilic displacement (before or after cycloaddition) of the selectively reactive 5-chlorine atom provides a rapid access to stable 5-methylene-1,3,4-thiadiazolines.