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Catalytic Enantioselective Reaction of 2H-Azirines with Thiols Using Cinchona Alkaloid Sulfonamide Catalysts
Organic Letters ( IF 5.2 ) Pub Date : 2018-01-19 00:00:00 , DOI: 10.1021/acs.orglett.7b04022
Shuichi Nakamura 1, 2 , Daiki Hayama 1 , Masataka Miura 1 , Tsubasa Hatanaka 3 , Yasuhiro Funahashi 3
Affiliation  

The first catalytic enantioselective reaction of 2H-azirines with thiols has been developed. The obtained aziridines can be converted to optically active oxazolines, aziridylamides, or α-sulfonyl esters. Transformation of these optically active aziridines showed that 2H-azirines act as β,β-dicarbocationic amine synthons.

中文翻译:

Cinchona生物碱磺酰胺催化剂催化2 H-偶氮与硫醇的对映选择性反应

已经开发出2 H-叠氮基与硫醇的第一催化对映选择性反应。所获得的氮丙啶可以转化为光学活性的恶唑啉,叠氮基酰胺或α-磺酰基酯。这些旋光性氮丙啶的转化表明,2 H-氮丙啶可作为β,β-二碳并氨基胺合成子。
更新日期:2018-01-19
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