134746-37-5Relevant articles and documents
Acid Chlorides as Formal Carbon Dianion Linchpin Reagents in the Aluminum Chloride-Mediated Dieckmann Cyclization of Dicarboxylic Acids
Armaly, Ahlam M.,Bar, Sukanta,Schindler, Corinna S.
supporting information, p. 3962 - 3965 (2017/08/15)
The development of acid chlorides as formal dianion linchpin reagents that enable access to cyclic 2-alkyl- and 2-acyl-1,3-alkanediones from dicarboxylic acids is described herein. Mechanistic experiments relying on 13C-labeling studies confirm the role of acid chlorides as carbon dianion linchpin reagents and have led to a revised reaction mechanism for the aluminum(III)-mediated Dieckmann cyclization of dicarboxylic acids with acid chlorides.
SYNTHESIS OF (+/-)-ANGUSTIONE BY THE REGIOSELECTIVE ALKYLATION OF ENAMINODIKETONES UNDER THE ACTION OF STRONG BASES
Zenyuk, A. A.,Korchuk, A. V.,Ukhova, L. I.,Lis, G. L.
, p. 519 - 524 (2007/10/02)
The synthesis of (+/-)-angustione has been carried out on the basis of a method that we have developed for the regio- and stereoselective alkylation of enaminodiketones of the cyclohexane series.