Trends in lipase-catalyzed asymmetric access to enantiomerically pure/enriched compounds

Tipo de material: Texto

TextoSeries ; Tetrahedron, 63(8), p.1721-1754, 2007Trabajos contenidos:

Ghanem, A

Recursos en línea:

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

Resumen: Over the last few years, there has been a dramatic increase in the number of publications in the field of lipase-catalyzed reactions performed in common organic solvents, ionic liquids or even non-conventional solvents. A fairly large percentage of these publications have emerged from organic chemists who have recognized the potential of biocatalysis as a viable and popular technique in organic synthesis. Considerable research has shown that reactions catalyzed by enzymes are more selective and efficiently performed than many of their analogues in the organic chemistry laboratory. This review article focuses on some of the recent developments in the rapidly growing field of lipase-catalyzed asymmetric access to enantiomerically pure/enriched compounds. The literature search is dated back to the last five years and covers some comprehensive examples.

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-12942 (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-1294 Properties and fields of application of the new fabric Tural	B-12940 10-oxo-cylindrocarpidin, ein neues alkaloid aus tabernaemontana amygdalifolia.	B-12941 Homocylindrocarpidine and 17-demethoxy-xylindrocarpidine, 2 new alkaloidas from Tabernaemontana amygdalifolia	B-12942 Trends in lipase-catalyzed asymmetric access to enantiomerically pure/enriched compounds	B-12943 The New Pentacyclic Saponine Ecdysantherin [3/9-Hydroxy-20-methylpregn-5,14- dien- 16-one-(18-20 )-lactone ] from Ecdysanthera rosea Hook. et Am. (Apocynaceae)of Vietnam	B-12944 Stress concentrations in filamentary structures	B-12945 Rice blast fungus transcriptomics	Next

Over the last few years, there has been a dramatic increase in the number of publications in the field of lipase-catalyzed reactions performed in common organic solvents, ionic liquids or even non-conventional solvents. A fairly large percentage of these publications have emerged from organic chemists who have recognized the potential of biocatalysis as a viable and popular technique in organic synthesis. Considerable research has shown that reactions catalyzed by enzymes are more selective and efficiently performed than many of their analogues in the organic chemistry laboratory. This review article focuses on some of the recent developments in the rapidly growing field of lipase-catalyzed asymmetric access to enantiomerically pure/enriched compounds. The literature search is dated back to the last five years and covers some comprehensive examples.

There are no comments on this title.

to post a comment.