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Highly Enantioselective Hydrogenation of tetra-and tri-Substitutedα,β-Unsaturated Carboxylic Acids with oxa-Spiro Diphosphine Ligands 被引量:3
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作者 Gen-Qiang Chen Jia-Ming Huang +6 位作者 bi-jin lin Chuan Shi ling-Yu Zhao Bao-De Ma Xiao-Bing Ding Qin Yin Xumu Zhang 《CCS Chemistry》 CAS 2020年第6期468-477,共10页
We herein present the design and synthesis of a structurally unique oxa-spirocyclic diphosphine ligand,termed as O-SDP.The diphosphine ligand O-SDP derived from oxa-spirocyclic diphenols(O-SPINOL)has a relatively larg... We herein present the design and synthesis of a structurally unique oxa-spirocyclic diphosphine ligand,termed as O-SDP.The diphosphine ligand O-SDP derived from oxa-spirocyclic diphenols(O-SPINOL)has a relatively larger bite angle compared with that of SDP,and O-SDP has been successfully applied in the ruthenium-catalyzed asymmetric hydrogenation ofα,β-unsaturated carboxylic acids under mild reaction conditions.High yields and enantioselectivities were generally achieved for a wide range of substrates(up to 99%yield and>99%ee),and many of the resulting products are key intermediates of important drugs such as Sacubitril,Artemisinin,and Paroxetine. 展开更多
关键词 asymmetric hydrogenation DIPHOSPHINE O-SDP O-SPINOL
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