Helvetica Chimica Acta p. 1600 - 1607 (1991)
Update date:2022-08-02
Topics: Diastereoselectivity Radical reactions Column chromatography NMR spectroscopy Enantioselectivity Steric hindrance Enantiomeric excess (ee) Recrystallization Stereoselective synthesis TLC (thin-layer chromatography) Protecting group Chiral Auxiliary Quenching Radical Initiation Radical intermediate Diastereomeric ratio (dr)
Bulliard, Michel
Zehnder, Margareta
Giese, Bernd
Radical addition to 2-cyclohexyl-5-methylidene-6-methyl-1,3-dioxan-4-one (2) affords stereoselectively 5,6-trans-products trans-3.The size of the radical has no influence on the selectivity.These trans-acetals are converted into threo-3-hydroxy-butanoates
View MoreShanghai Pinewood Fine Chemical Co., Ltd.
website:http://www.pinewoodchem.com
Contact:0086-21-62417129，62414096
Address:Suite B, 27F, No.2, Lane 600, Tianshan Road, Shanghai
Zhejiang Sanmei Chemical Industry Co., Ltd
Contact:86-579-87633213
Address:Huchu Industrial Zone, Qingnian Rd., Wuyi County, Zhejiang Prov., China.
Contact:
Address:308# dongwu avenue dongxihu district wuhan city
Suzhou Sinosun Imp.&Exp. Corporation
website:http://www.szsinosun.com
Contact:+86-512-63488895,63488616
Address:No.758 East Jiangling Road Wujiang Economic & Technological Developmenty Zone Jiangsu China
Contact:+86-21-54391580
Address:Room 502,No.65,Lane 2388 Hongxin Road,Shanghai,China
Doi:10.1021/jo00028a012
(1992)Doi:10.1016/j.molstruc.2012.02.054
(2012)Doi:10.1055/s-0031-1290610
(2012)Doi:10.1271/bbb.110829
(2012)Doi:10.1021/jm00086a006
(1992)Doi:10.1021/ja00026a026
(1991)
