630115-35-4Relevant academic research and scientific papers
An efficient ring-closing metathesis reaction of geminally disubstituted olefins using first generation Grubbs' catalyst: Enantiospecific synthesis of pacifigorgianes
Srikrishna,Dethe, Dattatraya H.
, p. 7817 - 7820 (2003)
An efficient ring closing metathesis reaction with first generation Grubbs' catalyst [PhCH=RuCl2(PCy3)2] involving geminally disubstituted olefins has been discovered. It has been extended to the enantiospecific synthesis of pacifigorgiane sesquiterpenes.
