77094-95-2Relevant articles and documents
Lewis Acid-Catalyzed [3+3] Annulation of Donor-Acceptor Cyclopropanes and Indonyl Alcohols: One Step Synthesis of Substituted Carbazoles with Promising Photophysical Properties
Varshnaya, Rohit Kumar,Banerjee, Prabal
, p. 1614 - 1623 (2019/02/07)
A highly efficient protocol to access carbazole from donor-acceptor cyclopropane and indonyl alcohol via [3+3] annulation in the presence of a Lewis acid has been demonstrated. This method facilitates the post functionalization of the substituted carbazol
Synthesis of Indenopyridine Derivatives via MgI2-Promoted [2+4] Cycloaddition Reaction of In-situ Generated 2-Styrylmalonate from Donor-Acceptor Cyclopropanes and Chalconimines
Verma, Kamal,Banerjee, Prabal
supporting information, p. 3687 - 3692 (2018/10/15)
An unexpected MgI2-promoted [2+4] cycloaddition reaction of in-situ generated 2-styrylmalonate from donor-acceptor cyclopropanes with chalconimines to synthesize highly substituted indenopyridine derivatives under the mild reaction conditions h
(3 + 3)-cyclodimerization of donor-acceptor cyclopropanes. three routes to six-membered rings
Ivanova, Olga A.,Budynina, Ekaterina M.,Chagarovskiy, Alexey O.,Trushkov, Igor V.,Melnikov, Mikhail Ya.
experimental part, p. 8852 - 8868 (2012/01/02)
The ability of donor-acceptor cyclopropanes to (3 + 3)-cyclodimerize is disclosed. It has been found that Lewis acid-induced transformations of 2-(hetero)arylcyclopropane-1,1-dicarboxylates containing electron-abundant aromatic substituents led to the con
