Journal of the Chemical Society. Chemical communications p. 734 - 735 (1981)
Update date:2022-08-03
Topics: Yield NMR spectroscopy Enantiomeric excess (ee) Stereoselective synthesis Total synthesis Optical rotation Asymmetric catalysis HPLC (high-performance liquid chromatography) Protecting group X-ray crystallography Retrosynthetic analysis Chiral Auxiliary Ring-Closing Metathesis Diterpene Lactonization Stereocenter Marine Natural Product
Imamura, Paulo M.
Sierra, Manuel Gonzalez
Ruveda, Edmundo A.
The synthesis of (+)-isoagatholactone (1) from (+)-manool (4) via the key intermediate ent-methyl isocopalate (2) is described.
View MoreContact:86-511-85210668 0511-85210668, 85210818, 85210898
Address:Yihai Garden E-902,NO.99 Daxi RD., Zhenjiang Jiiangsu ,China
website:http://www.enbridgepharm.com
Contact:+86-510-83591909
Address:Huishan Zone, Wuxi City, Jiangsu Province, P.R.China
Hubei Sibo Technology Co.,Ltd.
Contact:0715-6597222
Address:Pan Jia Wan fan Lake Chemical Industrial Park ,Xianning City, Hubei, China
website:http://www.angchenchem.com
Contact:+86-510-88302099 82327577
Address:Rm. 404/405, Floor 4th, No. 983 FengXiang Road, Wuxi, China
Contact:86-607-68073220
Address:1 ave na road jiahua st
Doi:10.1007/BF00988238
(1979)Doi:10.1021/jo00330a048
(1981)Doi:10.1016/j.bmc.2003.10.004
(2004)Doi:10.1039/DT9780000110
()Doi:10.1016/0032-3950(78)90361-1
(1978)Doi:10.1021/ja01138a006
(1952)
