474925-46-7

Upstream product

• 38025-45-5 1-benzyl-4-phenyl-1,2,3,6-tetrahydro-pyridine 
• 474924-68-0 (4-methoxy-phenyl)-(5-nitro-3-phenyl-pent-1-enyl)-carbamic acid tert-butyl ester 
• 474925-60-5 5-nitro-3-phenyl-pentanoic acid methyl ester 
• 1026978-20-0 (S)-5-Nitro-3-phenyl-pentanoic acid 
• 474924-87-3 (S)-4-phenylpiperidin-2-one 
• 100-39-0 benzyl bromide 
• 474924-98-6 (S)-N-benzyl-4-phenyl-2-piperidinone 

Relevant academic research and scientific papers

Asymmetric carbon-carbon bond formations in conjugate additions of lithiated N-Boc allylic and benzylic amines to nitroalkenes: Enantioselective synthesis of substituted piperidines, pyrrolidines, and pyrimidinones

(-)-Sparteine mediated lithiations of N-Boc-allylic and benzylic amines provide configurationally stable intermediates which on conjugate additions to nitroalkenes provide highly enantioenriched enecarbamate products in good yields, and with high diastere

[2]Benzopyrano[3,4-c]pyridines and process therefor

[2]Benzopyrano[3,4-c]pyridine derivatives characterized by having a 2,3,4,4a,6,10b-hexahydro-1H-[2]benzopyrano[3,4-c]pyridine nucleus bearing a substituent at position 6 are disclosed. The nucleus can be optionally further substituted at positions 2,3,4,6 and on the aromatic ring. The derivatives are useful diuretic, anorexic, antidepressant, anticonvulsant and antihypertensive agents. Methods for their preparation and use also are disclosed.