Stereoselective elaboration of the tricyclo[9.3.1.03,8]pentadecane ring system. Atropisomeric control of stereochemistry
作者:Randy W. Jackson、Richard G. Higby、Kenneth J. Shea
DOI:10.1016/s0040-4039(00)61261-3
日期:1992.8
The chemistry of a conformationally locked tricyclo[9.3.1.03,8]pentadecane skeleton, prepared by an atropselective type 2 intramolecular Diels-Alder reaction, is examined. In many cases, the conformation of the tricycle controls the facial selectivity of the addition of nucleophilic and electrophilic reagents to this ring system.