Journal of the Chemical Society. Chemical communications p. 789 - 790 (1994)
Update date:2022-08-03
Topics:
Kido, Fusao
Yamaji, Kazuo
Sinha, Subhash C.
Yoshikoshi, Akira
Kato, Michiharu
The rhodium(II)-catalysed cyclisation of acyclic α-diazomalonate 1b and α-diazo-β-keto esters 1c, d give stereoselectively the highly substituted δ-lactone 3b and cyclohexanones 3c, d respectively, by <2,3>sigmatropic rearrangement via the stereocontrolle
View Moreshanghai hekang chemical co.ltd
Contact:021-54173790
Address:328 WuHe Road, Building #A, 2nd Floor, Minhang, Shanghai 201109, China
Disynthesis Chemical Technology Co. Ltd.
Contact:+86-571-88194596
Address:Dengyun road 380, Gongshu district, Hangzhou city, China
Shanghai Hongbang Medical Technology CO.,. Ltd
Contact:13671516988 /18917636693
Address:Room1, No67 Building, Yongde Road369, Wujing Town, Minhang Districy, Shanghai CIty, China.
Ningbo Inno Pharmchem Co., Ltd.
Contact:86-574-87319282
Address:6F-5,NO.163 RUIQING RD.,NINGBO 315000 CHINA
ShangHai Ruiyi Medical Technology Co.,Ltd.
Contact:+86-21-54718086
Address:No951 Jianchuan RD，Minhang District
Doi:10.1016/S0040-4020(01)92367-1
(1981)Doi:10.1002/jlcr.2580360803
(1995)Doi:10.1021/ja00146a039
(1995)Doi:10.1002/anie.199514491
(1995)Doi:10.1016/S0960-894X(99)00286-3
(1999)Doi:10.1002/recl.19951140607
(1995)
