141375-87-3Relevant articles and documents
Two-step allylic carbon insertion between ketone carbonyl and α carbons giving α-quaternary α-vinyl ketones
He, Jing-Qian,Shibata, Daisuke,Ohno, Chihaya,Okamoto, Sentaro
scheme or table, p. 6724 - 6727 (2009/04/07)
Ketones 1 were converted to α-quaternary α-vinyl ketones 2 by a two-step formal allylic carbon insertion between ketone carbonyl and α carbons, which involves the reaction of 1 with propargyltitanium reagents, derived from propargyl carbonates 3 and a divalent titanium reagent Ti(O-i-Pr)4/2i-PrMgCl, and the following rearrangement of the resulting α-allenyl alcohols 4 with NBS.