1245646-49-4Relevant articles and documents
Highly Enantioselective Catalytic Addition of Grignard Reagents to N-Heterocyclic Acceptors
Guo, Yafei,Harutyunyan, Syuzanna R.
, p. 12950 - 12954 (2019/08/07)
General methods to prepare chiral N-heterocyclic molecular scaffolds are greatly sought after because of their significance in medicinal chemistry. Described here is the first general catalytic methodology to access a wide variety of chiral 2- and 4-substituted tetrahydro-quinolones, dihydro-4-pyridones, and piperidones with excellent yields and enantioselectivities, utilizing a single catalyst system.
Gold(I)-catalyzed cycloisomerization of the mixed wys-acetals generated from homopropargylic amines; mechanistic implication for the formal alkyne prins reaction
Kim, Cheoljae,Lim, Wontaeck,Rhee, Young Ho
scheme or table, p. 1465 - 1466 (2010/10/19)
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