18691-32-2Relevant articles and documents
One-pot, fast cyclopropanation reaction of indandione with various aldehydes in the presence of cyanogen bromide and trimethylamine
Aalinejad, Michael,Noroozi Pesyan, Nader
, p. 1523 - 1530 (2019/05/10)
A new, fast, and easy one-pot cyclopropanation reaction of aromatic and aliphatic aldehydes with 1H-indene-1,3(2H)-dione and cyanogen bromide (BrCN) was developed for synthesizing 3′-(aryl[alkyl])-dispiro[indan-2,1′-cyclopropane-2′,2′′-indan]-1,1′′,3,3′′-
Selective formation of spiro dihydrofurans and cyclopropanes through unexpected reaction of aldehydes with 1,3-dicarbonyl compounds
Wang, Guan-Wu,Gao, Jie
supporting information; experimental part, p. 2385 - 2388 (2009/10/10)
An efficient methodology for the oxidative addition reaction of various aldehydes with 5,5-dimethylcyclohexane-1,3-dione and 1,3-indandione to selectively afford spiro dihydrofuran and cyclopropane derivatives, promoted by molecular iodine and dimethylami