Synthesis of α-thiohemiaminal derivatives of deoxynupharidine
RT Lalonde, TS Eckert
Index: LaLonde, Robert T.; Eckert, Timothy S. Canadian Journal of Chemistry, 1981 , vol. 59, p. 2298 - 2302
Full Text: HTML
Citation Number: 4
Abstract
Disulfides, sulfenyl chlorides, thiosulfonates, and sulfensuccinimides were evaluated as electrophilic thiating agents for converting the enamine 6-dehydrodeoxynupharidine to α- thiohemiaminal derivatives of the alkaloid deoxynupharidine. Sulfensuccinimides were generally the most useful but other types of agents produced better yields in some individual cases.
Related Articles:
[Henke, Adam; Srogl, Jiri Journal of Organic Chemistry, 2008 , vol. 73, # 19 p. 7783 - 7784]
[Groebel Chemische Berichte, 1959 , vol. 92, p. 2887,2891]