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Pd-Catalyzed Enantioselective Desymmetrizing 1,7-Enyne Cycloisomerization of Alkyne-Tethered Cyclopentenes
Organic Letters ( IF 5.2 ) Pub Date : 2024-05-12 , DOI: 10.1021/acs.orglett.4c01507
Ren-Xiao Liang 1 , Chao Ding 1 , Hu-Jie Cai 1 , Jia-Yi Wang 1 , Qi-Chuang Li 1 , Gao-Yang Yu 1 , Yi-Xia Jia 2, 3
Affiliation  

An enantioselective Pd-catalyzed intramolecular desymmetrizing cycloisomerization of N-(cyclopent-3-en-1-yl)propiolamides has been developed by employing a new chiral phosphoramidite ligand. A series of structurally unique bridged azabicycles are achieved in moderate to excellent yields with good E/Z selectivity and high enantioselectivity. Synthetic transformations are conducted to demonstrate the practical utility of this reaction.

中文翻译:


Pd 催化炔系环戊烯的对映选择性去对称 1,7-烯炔环异构化



通过采用新的手性亚磷酰胺配体,开发了 N-(环戊-3-en-1-基)丙酰胺的对映选择性 Pd 催化分子内去对称环异构化。一系列结构独特的桥联氮杂二环化合物以中等至优异的产率获得,并具有良好的 E/Z 选择性和高对映选择性。进行合成转化以证明该反应的实际用途。
更新日期:2024-05-12
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