Nitrilase-catalysed hydrolysis of cyanomethyl p-tolyl sulfoxide: stereochemistry and mechanism

P Kiełbasiński, M Rachwalski, M Mikołajczyk…

Index: Kielbasinski, Piotr; Rachwalski, Michal; Mikolajczyk, Marian; Rutjes, Floris P.J.T. Tetrahedron Asymmetry, 2008 , vol. 19, # 5 p. 562 - 567

Full Text: HTML

Citation Number: 9

Abstract

Several commercially available nitrilases have been used for the enantioselective hydrolysis of cyanomethyl p-tolyl sulfoxide into the corresponding amide and acid, which are formed in different proportions and with varying stereoselectivities, depending on the nitrilase involved. It was shown that the externally added amide is not transformed into the acid, which can be explained by assuming that both products must be produced in concurrent ...

Related Articles:

Ligand exchange reaction of sulfoxides in organic synthesis: A novel method for generation of magnesium enolates and its application to synthesis of [α]- …

[Satoh; Kitoh; Onda; Takano; Yamakawa Tetrahedron, 1994 , vol. 50, # 17 p. 4957 - 4972]

Ligand exchange reaction of sulfoxides in organic synthesis: A new method for generation of magnesium enolates of α-chloro carboxylic acids and their derivatives

[Satoh, Tsuyoshi; Kitoh, Yasushi; Onda, Ken-ichi; Yamakawa, Koji Tetrahedron Letters, 1993 , vol. 34, # 14 p. 2331 - 2334]

More Articles...