78604-93-0Relevant articles and documents
Cycloaddition of Nitrile Imines with Enamides: An Approach to Functionalized Pyrazolines and Pyrazoles
Tu, Liang,Gao, Limei,Wang, Xiaomeng,Shi, Ruijie,Ma, Rupei,Li, Junfei,Lan, Xiaoshuang,Zheng, Yongsheng,Liu, Jikai
supporting information, p. 559 - 573 (2021/01/09)
An efficient [3 + 2] cycloaddition of in situ generated nitrile imines with enamides has been established. A wide range of functionalized pyrazoline derivatives (53 examples) were obtained in moderate to good yields (up to 96%) under very mild conditions. This protocol features broad substrate scope, good functional group tolerance, and operational simplicity. Practical transformation of the products into useful pyrazoles via a one-pot process and the scalability of this protocol highlight the utility of this synthetic methodology.
AlCl3-promoted reaction of cycloalkanones with hydrazones: a convenient direct synthesis of 4,5,6,7-tetrahydro-1H-indazoles and their analogues
Laroum, Rima,Berrée, Fabienne,Roisnel, Thierry,Dorcet, Vincent,Carboni, Bertrand,Debache, Abdelmadjid
supporting information, (2019/08/07)
The AlCl3-promoted reactions of cycloalkanones with hydrazones are described. This approach represents a mild and operationally simple method to access 2,3-diaryl-4,5,6,7-tetrahydro-1H-indazoles and their analogues in good to moderate yields.
REGIOSELECTIVITY AND SPECIFICITY IN CYCLOADDITION OF DIPHENYLNITRILIMINE
Kitane, Said,Kabula, Tshiamala,Vebrel, Joel,Laude, Bernard
, p. 1217 - 1218 (2007/10/02)
Diphenylnitrilimine cycloaddition reactions on 1,2-dihydronaphtalenes are only regioselective.Use of 1- or 2-tetralones enamines as dipolarophiles allows to attain regiospecificity.