The influence of catalyst in reaction 36620-11-8

The article 《Catalytic Asymmetric Hydrogenation of Tetrasubstituted Unsaturated Lactams: An Efficient Approach to Enantioenriched 3,4-Disubstituted Piperidines》 also mentions many details about this compound(36620-11-8)Category: quinuclidine, you can pay attention to it, because details determine success or failure

Category: quinuclidine. The fused heterocycle is formed by combining a benzene ring with a single heterocycle, or two or more single heterocycles. Compound: Bis(norbornadiene)rhodium (I) tetrafluoroborate, is researched, Molecular C14H8BF4Rh, CAS is 36620-11-8, about Catalytic Asymmetric Hydrogenation of Tetrasubstituted Unsaturated Lactams: An Efficient Approach to Enantioenriched 3,4-Disubstituted Piperidines. Author is Yin, Congcong; Pan, Yingmin; Zhang, Xumu; Yin, Qin.

An unprecedented Rh-catalyzed enantioselective and diastereoselective hydrogenation of easily accessed α,β-disubstituted unsaturated lactams I (R = Ph, Me, cyclohexyl, thiophen-2-yl, etc.; R1 = Me, ethyl; X = 4-methoxyphenyl, benzyl, methyl) to afford synthetically valuable chiral lactams II with 1,2-consecutive stereocenters was reported. The reaction could be performed on gram scale and the products could be concisely transformed to enantiomerically pure trans-3,4-disubstitituted piperidines [such as (+)-femoxetin, (-)-paroxetine] which are prevalent structural units existed in medicinal agents.

The article 《Catalytic Asymmetric Hydrogenation of Tetrasubstituted Unsaturated Lactams: An Efficient Approach to Enantioenriched 3,4-Disubstituted Piperidines》 also mentions many details about this compound(36620-11-8)Category: quinuclidine, you can pay attention to it, because details determine success or failure

Reference:
Quinuclidine – Wikipedia,
Quinuclidine | C7H13N | ChemSpider