Helvetica Chimica Acta p. 1273 - 1286 (1986)
Update date:2022-07-31
Topics: Regioselectivity Characterization Yield Synthetic route Functionalized Deprotection Protecting group Tertiary alcohol Retrosynthetic analysis Diels-Alder Reaction Stereoselectivity Cycloaddition Catalysis Dienophile Diene Avermectins Milbemycins Hexahydrobenzofuran Macrocyclic lactone
Ireland, Robert E.
Obrecht, Daniel M.
A highly regio- and stereoselective Diels-Alder reaction between dienophiles of type I and dienes of type II (Scheme 1) gives rise to Diels-Alder adducts of type III.Upon treatment with BF3*Et2O, these adducts are smoothly converted into the corresponding
View MoreSuzhou Sibian Chemical Technology Co., Ltd
website:http://www.sibianpharm.com
Contact:+8618169181984,+8618013186906
Address:Room1404,BuildingA,Jiabao Square No.323 Baodai East Road,Wuzhong District,Suzhou Jiangsu China (215128)
Zhejiang Chemicals Import & Export Corporation
Contact:86-571-87043088
Address:No.37,Qingchun Road,Hangzhou,China
shanghai tuomiao chemicial co.,ltd.
website:https://www.tuomiaochem.com/
Contact:021 - 59853336
Address:shanghai
Ningxia Soochow Agrochemical Limited Company
Contact:(+86）0512 6320 8190
Address:wujiang
Contact:+49-9398-993127
Address:Untertorstr. 27
Doi:10.1021/acs.jmedchem.1c00837
(2021)Doi:10.1021/jm9700068
(1997)Doi:10.1021/acs.jmedchem.1c00374
(2021)Doi:10.1016/S0040-4039(01)93858-4
(1989)Doi:10.1039/c0nj00544d
(2011)Doi:10.1016/j.ica.2018.05.041
(2018)
