๐”– Bobbio Scriptorium
โœฆ   LIBER   โœฆ

Enzymatic Kinetic Resolution of 5-Hydroxy-4-oxa- endo- tricyclo[5.2.1.0 2,6 ]dec-8-en-3-ones: A Useful Approach to D-Ring Synthons for Strigol Analogues with Remarkable Stereoselectivity

โœ Scribed by Thuring, Jan Willem J. F.; Nefkens, Gerard H. L.; Wegman, Margreth A.; Klunder, Antonius J. H.; Zwanenburg, Binne

Book ID
126302432
Publisher
American Chemical Society
Year
1996
Tongue
English
Weight
220 KB
Volume
61
Category
Article
ISSN
0022-3263

No coin nor oath required. For personal study only.

๐Ÿ“œ SIMILAR VOLUMES

ChemInform Abstract: Enzymatic Kinetic R
ChemInform Abstract: Enzymatic Kinetic Resolution of 5-Hydroxy-4-oxa-endo-tricyclo(5.2.1.02, 6)dec-8-en-3-ones: A Useful Approach to D-Ring Synthons for Strigol Analogues with Remarkable Stereoselectivity.
โœ J. W. J. F. THURING; G. H. L. NEFKENS; M. A. WEGMAN; A. J. H. KLUNDER; B. ZWANEN ๐Ÿ“‚ Article ๐Ÿ“… 2010 ๐Ÿ› John Wiley and Sons โš– 36 KB ๐Ÿ‘ 1 views

## Enzymatic Kinetic Resolution of 5-Hydroxy-4-oxa-endotricyclo(5.2.1.02, 6)dec-8-en-3-ones: A Useful Approach to D-Ring Synthons for Strigol Analogues with Remarkable Stereoselectivity. -Racemic tricyclic hydroxy lactones (I) and (V) are resolved employing a lipase-catalyzed acetylation reaction