3-Hydroxy-4-methylthiazole-2 (3H)-thione carbamates (TTOC carbamates). Useful precursors for monoalkylaminium cation radicals
M Newcomb, KA Weber
Index: Newcomb, Martin; Weber, Karl A. Journal of Organic Chemistry, 1991 , vol. 56, # 3 p. 1309 - 1313
Full Text: HTML
Citation Number: 28
Abstract
Monoalkylaminium cation radicals have not been studied extensively. Neale and Marcus5 showed that monoalkylchloramines reacted in UV-initiated radical chain reactions under strongly acidic conditions (H2S04, AcOH) to give monoalkylaminium cation radicals that added to simple olefins. The ultimate products of the reactions, P-chloro amines, were obtained in fair to good yields. The products and yields were comparable to those ...
Related Articles:
Synthesis of disulfides via sulfenylation of alkyl and aryldithiopyridine N-oxides
[Barton, Derek H. R.; Chen, Chen; Wall, G. Michael Tetrahedron, 1991 , vol. <32> 47, p. 6127 - 6138]
[Barton, Derek H. R.; Crich, David; Motherwell, William B. Tetrahedron, 1985 , vol. 41, # 19 p. 3901 - 3924]
Synthesis of disulfides via sulfenylation of alkyl and aryldithiopyridine N-oxides
[Barton, Derek H. R.; Chen, Chen; Wall, G. Michael Tetrahedron, 1991 , vol. <32> 47, p. 6127 - 6138]
Synthesis of disulfides via sulfenylation of alkyl and aryldithiopyridine N-oxides
[Barton, Derek H. R.; Chen, Chen; Wall, G. Michael Tetrahedron, 1991 , vol. <32> 47, p. 6127 - 6138]
Synthesis of disulfides via sulfenylation of alkyl and aryldithiopyridine N-oxides
[Barton, Derek H. R.; Chen, Chen; Wall, G. Michael Tetrahedron, 1991 , vol. <32> 47, p. 6127 - 6138]