磷化氢
产量(工程)
对映选择合成
化学
催化作用
有机化学
药物化学
组合化学
材料科学
冶金
作者
Shin‐ichi Hirashima,E. Hirota,Yasuyuki Matsushima,Naoki Noda,Yuya Nishimura,Takefumi Narushima,Kosuke Nakashima,Tsuyoshi Miura
标识
DOI:10.1002/asia.202200989
摘要
The organocatalytic enantioselective hydrophosphinylation of various secondary phosphine sulfides with aromatic and aliphatic nitroalkenes is presented in this study. The reaction produced chiral β-nitrophosphine sulfides with excellent yields and enantioselectivities (up to 99% yield and 99% ee). Furthermore, the chiral β-nitrophosphine sulfides can be easily converted into α-substituted β-aminophosphine, which is a family of useful P, N-ligands and phosphine catalysts.
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