ENANTIOSELECTIVE BACTERIAL BIOTRANSFORMATION ROUTES TO CIS-DIOL METABOLITES OF MONOSUBSTITUTED BENZENES, NAPHTHALENE AND BENZOCYCLOALKENES OF EITHER ABSOLUTE-CONFIGURATION


Autoria(s): Allen, Christopher; Boyd, D.R.; Dalton, H.; Sharma, N.D.; Brannigan, I.; Kerley, N.A.; Sheldrake, G.N.; Taylor, S.C.
Data(s)

1995

Resumo

Enzyme-catalysed kinetic resolution and asymmetric dihydroxylation routes to enantiopure cis-diol metabolites of arenes and benzocycloalkenes of either absolute configuration have been developed using appropriate strains of the bacterium Pseudomonas putida.

Identificador

http://pure.qub.ac.uk/portal/en/publications/enantioselective-bacterial-biotransformation-routes-to-cisdiol-metabolites-of-monosubstituted-benzenes-naphthalene-and-benzocycloalkenes-of-either-absoluteconfiguration(cf219017-a63f-43dc-a9a2-509f11b3b493).html

http://dx.doi.org/10.1039/c39950000117

Idioma(s)

eng

Direitos

info:eu-repo/semantics/restrictedAccess

Fonte

Allen , C , Boyd , D R , Dalton , H , Sharma , N D , Brannigan , I , Kerley , N A , Sheldrake , G N & Taylor , S C 1995 , ' ENANTIOSELECTIVE BACTERIAL BIOTRANSFORMATION ROUTES TO CIS-DIOL METABOLITES OF MONOSUBSTITUTED BENZENES, NAPHTHALENE AND BENZOCYCLOALKENES OF EITHER ABSOLUTE-CONFIGURATION ' Chemical Communications , vol NA , pp. 117-118 . DOI: 10.1039/c39950000117

Tipo

article