期刊
SYNLETT
卷 -, 期 8, 页码 1227-1232出版社
GEORG THIEME VERLAG KG
DOI: 10.1055/s-0028-1088133
关键词
benzyltriethylammonium tetrathiomolybdate; beta-amino disulfides; sulfamidates; cystine; peptides
资金
- CSIR New Delhi
- IISc
Herein, we report a simple and efficient methodology for the synthesis of beta-amino disulfides by regioselective ring opening of sulfamidates with benzyltriethylammonium tetrathiomolybdate [BnNEt3](2)MoS4. Stability and reactivity of different protecting groups under the reaction conditions have been discussed. This methodology has also been extended to serine and threonine derived sulfamidates to furnish cystine and 3,3'-dimethyl cystine derivatives.
作者
我是这篇论文的作者
点击您的名字以认领此论文并将其添加到您的个人资料中。
推荐
暂无数据