Tetrahedron Letters p. 4949 - 4952 (1982)
Update date:2022-08-03
Topics:
Barton, Derek H.R.
Lusinchi, Xavier
Milliet, Pierre
Phenylseleninic anhydride reacts rapidly with indolines at 0 deg C to give, when the β-position is substituted, the corresponding indoles.When the β-position is unsubstituted β-phenylselenoindoles are formed.These are readily reduced by nickel boride to the parent indole.Tetrahydroisoquinoline is dehydrogenated with comparable ease.Phenylseleninic acid is also an efficient agent for these dehydrogenations.
View MoreHangzhou LINGEBA Technology Co., Ltd.
Contact:+0086-571-87389059
Address:Office 1-913,NewYouth Plaza, GongShu Area, HangZhou,ZheJiang,P.R.China
NINGBO YINZHOU PRECISE COLOR CO.,LTD.
Contact:86-574-88139809 86-574-83033159
Address:Qiming Road,Yinzhou,Ningbo,China
Contact:0792-8228321
Address:10TH Floor No.121 binjiang Road Xunyang District
Zhangjiagang Golden Reach Fine Chemical Co.,LTD.
Contact:+86-512-6585 6968
Address:Changfu Road， Dongsha Chemical Industry Park, Zhangjiagang City, Jiangsu Province, China
Nanjing Spring & Autumn Biological Engineering Co., Ltd.
Contact:86-180510-83338
Address:Suite# 210, No. 1 BuildingNanjing Agricultural Biotechnology High-tech Entrepreneurship Center, No. 4 Tongwei Road, Xuanwu District, Nanjing,China
Doi:10.1039/c39860000872
(1986)Doi:10.1071/CH9851685
(1985)Doi:10.1039/b803043j
(2008)Doi:10.1016/j.tetlet.2008.05.043
(2008)Doi:10.1016/j.tet.2008.05.050
(2008)Doi:10.1016/S0040-4039(00)98247-9
(1985)
