85706-53-2Relevant articles and documents
Enantiospecific access to various C(9),C(10)-disubstituted camphors: Scope and limitations
Martinez, Antonio Garcia,Vilar, Enrique Teso,Fraile, Amelia Garcia,De La Moya Cerero, Santiago,Morillo, Cristina Diaz,Morillo, Rocio Perez
, p. 7348 - 7351 (2004)
The valuable chiral sources C(9),C(10)-disubstituted camphors can be enantiospecifically obtained from the corresponding C(9)-substituted camphors by a general and straightforward synthetic method. This method involves the electrophilic treatment of a key
An enantiospecific route to C,D ring synthons for steroid synthesis
Clase, J. Andrew,Money, Thomas
, p. 1537 - 1544 (2007/10/02)
A simple enantiospecific route to a hydrindenone intermediate for steroid synthesis has been accomplished.The introduction of a wide variety of side-chain units is made possible by stereoselective alkylation of a bicyclic ester 13 derived from (+)-camphor
Ring cleavage of camphor derivatives: formation of chiral synthons for natural products synthesis
Hutchinson, J. H.,Money, T.,Piper, S. E.
, p. 854 - 860 (2007/10/02)
Base-promoted ring cleavage of 9,10- and 8,10-dibromocamphor provides chiral intermediates for natural product synthesis.