94807-43-9Relevant academic research and scientific papers
THE REACTION OF VINYLBORONIC ACIDS WITH VINYLMERCURIC ACETATES; A NEW SYNTHESIS OF DIVINYLMERCURIALS
Varma, Rajender S.,Kunda, Sastry A.,Kabalka, George W.
, p. 311 - 316 (1984)
The reaction of vinylboronic acids with vinylmercuric acetates produces symmetrical divinylmercurials in high yield.The reaction can be utilized to prepare functionally substituted mercurials.Attempts to prepare unsymmetrical divinylmercurials resulted in redistribution products yielding symmetrical and unsymmetrical divinylmercury compounds.
SYNTHESES OF FUNCTIONALLY SUBSTITUTED DIVINYLMERCURY COMPOUNDS
Varma, Rajender S.,Kunda, Sastry A.,Kabalka, George W.
, p. 331 - 336 (2007/10/02)
Reductive disproportionation of vinylmercuric chlorides by alkaline sodium stannite produces divinylmercurials in high yields.The reaction conditions are optimized to obtain functionally substituted divinylmercurials in pure form, free from undesirable si
