
Tetrahedron Asymmetry p. 2597 - 2610 (1995)
Update date:2022-08-03
Topics:
Valk, Jean-Marc
Claridge, Timothy D. W.
Brown, John M.
Hibbs, David
Hursthouse, Michael B.
A synthesis of the title phosphinamine (PHENAP) is described, following previously established methodology.Resolution via the C,N-palladocycle derived from (R)-N,N-dimethyl-α-methyl-1-naphthylamine led to two crystallographically defined complexes with the (R,S)-form posessing a chelated ligand and the (R,R)-form open with only the phosphine coordinated.Palladium allyl complexes of the ligand were strikingly different from those of the corresponding isoquinoline ligand QUINAP, and the differences could be rationalised by recourse to molecular models, with the additional fused arene ring of PHENAP playing a critical part in defining the coordination sphere through its steric pressure.A brief appraisal of Pd-catalysed allylic alkylation reactions was performed with the new ligand.
View MoreFujian Wanke Pharmaceutical Co., LTD.
Contact:+86-598-5026002
Address:Economic development zone,jiangle county
Nanyang Tianhua pharmaceutical Co.,Ltd.
Contact:+8618639816203
Address:Longsheng Industrial Park
Buffett (China) Holding Co.,Ltd
Contact:4006570891
Address:
Hangzhou jls Flame Retardants Chemical Co.,Ltd
Contact:+86-571-87250387/87250386
Address:MOGANSHAN RODA 1418# SHANGCHENG INDUSTRIAL PARK
Shanghai Rainbow Chemistry Co., Ltd.
Contact:+86-21-64968086-5815/5812
Address:3rd floor, Building 7, 251 Faladi Road, Zhangjiang Hi-Tech Park, Pudong District, Shanghai, P.R. China
Doi:10.1002/jlcr.1164
(2007)Doi:10.1021/om030692a
(2004)Doi:10.1139/v66-302
(1966)Doi:10.1039/C39740000665
(1974)Doi:10.1016/S0040-4039(99)01052-7
(1999)Doi:10.1021/jm0498708
(2004)