Enantioselective Allylic Amination with Chiral (Phosphino-oxazoline)Pd Catalysts

DOI: 10.1016/0957-4166(94)80021-9

Source and publish data:

Tetrahedron Asymmetry p. 573 - 584 (1994)

Update date:2022-08-16

Topics:

Authors:

Matt, Peter von

Loiseleur, Olivier

Koch, Guido

Pfaltz, Andreas

Lefeber, Claudia

et al. et al.

Read Full Text PDF DownLoad Join now for total 90,000,000 free articles

Article abstract of DOI:10.1016/0957-4166(94)80021-9

Chiral (phosphinophenyl-oxazoline)palladium complexes have been studied as enantioselective catalysts for allylic amination using benzylamine or the sodium salts of p-toluenesulfonamide, benzoylhydrazine, and (Boc)2NH as nucleophiles.In the reactions with

Full text of DOI:10.1016/0957-4166(94)80021-9

Products guided by the article

Product name:(-)-(R,E)-N-benzyl-(1,3-diphenyl-2-propenyl)amine

Cas No:121440-75-3

R&D Labs maybe for 121440-75-3

Shanxi Tongji Pharmaceuticals Co., Ltd.

Contact:+86-359-3024784

Address:Xikuang South Road, Ruicheng County , Shanxi
JIN TAN CHENG'EN CHEMICAL CO.,LTD.

Contact:86-519-82116250

Address:NO.102，village Dongfang，conomic development zone
shanghai hekang chemical co.ltd

Contact:021-54173790

Address:328 WuHe Road, Building #A, 2nd Floor, Minhang, Shanghai 201109, China
Fujian Wanke Pharmaceutical Co., LTD.

Contact:+86-598-5026002

Address:Economic development zone,jiangle county
Hangzhou Share Chemical Co., Ltd(expird)

Contact:+86-57187093700

Address:Hang Xing Road

Relevant to this article

Tandem cyclisations involving α-ketenyl alkyl radicals. New syntheses of the natural triquinanes pentalenene and modhephene

Doi:10.1039/b413817c
(2005)
Remote C-H Activation of Quinolines through Copper-Catalyzed Radical Cross-Coupling

Doi:10.1002/asia.201501407
(2016)
Catalytic oxidation of para-substituted phenols with nitrogen dioxide and oxygen

Doi:10.1016/S0040-4039(98)00242-1
(1998)
The Structure and Characterization of 3,4,5-Triiodo-2-Methylthiophene: An Unexpected Iodination Product of 2-Methylthiophene

Doi:10.1007/s10870-019-00770-z
(2019)
Doi:10.1039/jr9590000487
(1959)
Doi:10.1021/ja01163a532
(1950)

Article Doi