Article ID | Journal | Published Year | Pages | File Type |
---|---|---|---|---|
10575592 | Journal of Organometallic Chemistry | 2005 | 7 Pages |
Abstract
The radical initiated reaction of 3 with (TMS)3SiH gave benzylmethylamine and thiosilane 5 as main products together with salt 7 as by-product. The amine obtained in a quantitative yield can arise from two independent routes of (TMS)3Si raidcal attack on 3. The minor attack on the ring affords 2-mercaptobenzothiazole that can act as a catalyst for the major route during the reaction course and then gives the salt 7 with amine. The reaction is a rare example of a radical chain-branching process and the origin of autocatalysis is discussed in some details.
Related Topics
Physical Sciences and Engineering
Chemistry
Inorganic Chemistry
Authors
Vladimir T. Varlamov, Carla Ferreri, Chryssostomos Chatgilialoglu,