Asymmetric Photocatalyzed Addition of Cyclic Ammes to the Chiral 5-(l)-Menthyloxy-2(5H)-furanone
Asymmetric Photocatalyzed Addition of Cyclic Ammes to the Chiral 5-(l)-Menthyloxy-2(5H)-furanone作者机构:Department of Chemistry Beijing Normal University Beijing 100875 China
出 版 物:《Chinese Chemical Letters》 (中国化学快报(英文版))
年 卷 期:1999年第10卷第11期
页 面:889-892页
核心收录:
学科分类:081704[工学-应用化学] 07[理学] 08[工学] 0817[工学-化学工程与技术] 070303[理学-有机化学] 0703[理学-化学]
主 题:Asymmetric photocatalysed conjugate addition enantiomerically pure C-Cphotoadducts. secondary cyclic amine enantiomerically pure N-C photoaducts.
摘 要:The benzophenone-initiated photoaddition of N-methyl ammes 2 to the chiral synthon1 proceeds in a regiospecitlc and highlyr stereocontrolled thshion to give the C-C photoadductscontaining a ne\viy stereogenic center 3a-3c. The enantiomerically pure N-C photoadducts, aminobutenolides 5a-5c have been obtained from the enantioselective photoaddition of secondary cyclicammes 4 with the chiral synthon 1 under the same conditions.