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Highly enantioselective reduction of β-amino nitroolefins with a simple n-sulfinyl urea as bifunctional catalyst

机译:以简单的亚磺酰基脲为双官能催化剂,高度对映选择性还原β-氨基硝基烯烃

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摘要

Simple but effective: A structurally simple N-sulfinyl urea was found to be a highly efficient bifunctional catalyst, which allows for the development of a novel pathway for the construction of chiral β-amino nitroalkanes through enantioselective reduction of β-amino nitroolefins by trichlorosilane. High yields and excellent enantioselectivities were obtained for a broad range of β-arylamino nitroolefin substrates (see scheme).
机译:简单但有效:发现结构简单的N-亚磺酰基尿素是一种高效的双功能催化剂,它允许通过三氯硅烷对映体选择性还原β-氨基硝基烯烃来开发构建手性β-氨基硝基烷烃的新途径。对于宽范围的β-芳基氨基硝基烯烃底物,均获得了高收率和出色的对映选择性(参见方案)。

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