Mehta, Goverdhan and Reddy, Srinivasa D (1999) Enzymatic resolution of dioxygenated dicyclopentadienes: Enantiopure hydrindanes, hydroisoquinolones, diquinanes and application to a synthesis of (+)-coronafacic acid. In: Tetrahedron Letters, 40 (5). pp. 991-994.
Enzymatic_Resolution_of_Dioxygenated.pdf - Published Version
Restricted to Repository staff only
Download (218Kb) | Request a copy
A 5, 10-dioxygenated-tricyclo[126.96.36.199(2,6)]decane derivative 6 has yielded to efficient enzymatic resolution to provide a range of chiral building blocks, whose absolute configuration has been determined through a total synthesis of naturally occuring (+)-coronafacic acid. (C) 1999 Elsevier Science Ltd. All rights reserved.
|Item Type:||Journal Article|
|Additional Information:||Copyright of this article belongs to Elsevier Science.|
|Department/Centre:||Division of Chemical Sciences > Organic Chemistry|
|Date Deposited:||23 Jun 2011 06:12|
|Last Modified:||23 Jun 2011 06:12|
Actions (login required)