期刊
TETRAHEDRON LETTERS
卷 56, 期 42, 页码 5747-5751出版社
PERGAMON-ELSEVIER SCIENCE LTD
DOI: 10.1016/j.tetlet.2015.09.022
关键词
N-Sulfonylimines; Carbamoylsilane; Amides; Addition; Synthetic methods
资金
- Shanxi Province Foundation for Returness [0713]
- Natural Science Foundation of Shanxi Province [2012011046-9]
- Foundation of Shanxi Normal University, China [SD2015CXXM-83]
N-Methoxymethyl-N-methylcarbamoyl(trimethyl)silane reacted with N-sulfonylimines in anhydrous benzene under catalyst-free conditions to afford alpha-(N-sulfonyl)amino-N-methoxymethyl-N-methylamides in good to excellent yields (71-95%). Furthermore, after acid hydrolysis at room temperature, the corresponding alpha-(N-sulfonyl)amino secondary amides can be formed. (C) 2015 Elsevier Ltd. All rights reserved.
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