Tetrahedron Letters p. 7469 - 7472 (1996)
Update date:2022-08-03
Topics:
Costello, Colleen A.
Kreuzman, Adam J.
Zmijewski, Milton J.
Phthalyl amidase selectively deprotects phthalimido groups under very mild aqueous conditions in a one-pot reaction to produce phthalic acid and the free amine. The enzyme has been shown to deprotect several primary amines of distinctly different structure, and exhibits chiral selectivity when the substrate contains extensive β-branching. The enzyme has a definite requirement for ortho positioning of the functional groups on a fixed axis of rotation.
View Morewebsite:http://www.apeptides.com/en/
Contact:+86-21-60871011
Address:No. 80 Chuanshan Shuyuan Steet,Pudong,Shanghai
Zhejiang Rongkai Chemical Technology Co.,Ltd.
Contact:+86-578-8185786
Address:Shangjiang Industrial Zone,Suichang
Hubei Danao Pharmaceutical Co.,Ltd.
website:http://www.danaopharm.com
Contact:+86-719-5251167
Address:Fandan Road,Danjiangkou,Hubei
Jining Shengrun Chemical Industry Co., Ltd.
Contact:+86-537-7121666 ,
Address:West Ring Road,Wenshang County Shandong Province
Xi'an North Information Industry Co., Ltd. Weilv Chemical Department
Contact:+86-29-88156413
Address:Jixiang Road 99 Xi'an Shaanxi Province
Doi:10.1016/S0040-4020(01)98848-9
(1981)Doi:10.1016/j.bmc.2004.08.043
(2004)Doi:10.1039/c39810001121
(1981)Doi:10.1002/ardp.19823150115
(1982)Doi:10.1016/j.cclet.2011.06.005
(2011)Doi:10.1016/j.bmcl.2015.06.021
(2015)
