Fungal hydroxylation of ethyl benzene and derivatives

Tipo de material: Texto

TextoSeries ; Tetrahedron Letters, 26(52), p.6409-6412, 1985Trabajos contenidos:

Holland, H.L
Carter, I.M
P. Chinna Chenchaiah
Khan, S.H
Munoz, B
Ninniss, R.W
Richards, D

Recursos en línea:

Para ver el documento ingresa a Google con tu cuenta: @cicy.edu.mx

Resumen: The fungus Mortierella isabellina converts ethyl benzene and a number of para- substituted derivatives to the corresponding optically active 1-phenylethanols with enantiomeric excesses between 5 and 40 per cent. Hydrogen removal from the substrate preceeds product formation and is stereochemically independent of it.

Tags from this library: No tags from this library for this title. Log in to add tags.

Average rating: 0.0 (0 votes)

Holdings
Item type	Current library	Collection	Call number	Status	Date due	Barcode
Documentos solicitados	CICY Documento préstamo interbibliotecario	Ref1	B-15269 (Browse shelf(Opens below))	Available

Browsing CICY shelves, Shelving location: Documento préstamo interbibliotecario, Collection: Ref1 Close shelf browser (Hides shelf browser)

Previous	No cover image available	No cover image available	No cover image available	No cover image available	No cover image available	No cover image available	No cover image available	Next
Previous	B-15266 Eucalyptin from Eugenia and myrcia species	B-15267 Leaf sectory structure and volatile compounds of Eugenia copacabanensis kiaersk. (Myrtaceae)	B-15268 Limnology in Mexico	B-15269 Fungal hydroxylation of ethyl benzene and derivatives	B-1527 Roles of G protein subunits in transmembrane signalling	B-15270 Removal of O-and N-benzyl groups by fungal biotransformation	B-15271 Fungal cytochrome P450s catalyzing hydroxylation of substituted toluenes to from their hydroxymethyl derivatives	Next

The fungus Mortierella isabellina converts ethyl benzene and a number of para- substituted derivatives to the corresponding optically active 1-phenylethanols with enantiomeric excesses between 5 and 40 per cent. Hydrogen removal from the substrate preceeds product formation and is stereochemically independent of it.

There are no comments on this title.

to post a comment.