1.
Mil Med Res
; 9(1): 41, 2022 07 16.
Article
in English
| MEDLINE
| ID: mdl-35841072
2.
Org Biomol Chem
; 12(22): 3562-6, 2014 Jun 14.
Article
in English
| MEDLINE
| ID: mdl-24676561
ABSTRACT
The first synthetic attempt commencing from an eight-membered ring to approach the [5.3.1] bicyclic core of vinigrol has demonstrated the feasibility of using the conformational bias of the cyclooctane-ring system to realize highly diastereoselective reactions. The synthetic potential of the newly disclosed access to in/out isomerism may stimulate broader interests.