作者:Andrzej Z. Rys、David N. Harpp
DOI:10.1016/s0040-4039(00)01249-1
日期:2000.9
Triphenylthiosulfenyl chloride (1) reacts with disulfides RSSR, yielding tetrasulfides as the main products. The results of the insertion for different R groups are reported. A two-step mechanism involving the formation of unsymmetrical trisulfide intermediates containing the trityl group is proposed. (C) 2000 Elsevier Science Ltd. All rights reserved.