855307-25-4

Upstream product

• 855307-24-3 2-{[(R)-2-(2-tert-butyldiphenylsilyloxy)-1-phenylethylamino]methyl}phenylamine 
• 24424-99-5 di-tert-butyl dicarbonate 
• 855307-23-2 (R)-2-(2-aminobenzylamino)-2-phenylethanol 
• 855307-22-1 (R)-2-(2-nitrobenzylamino)-2-phenylethanol 
• 56613-80-0 D-2-phenylglycinol 
• 552-89-6 2-nitro-benzaldehyde 

Downstream Products

• 855307-28-7 (R)-tert-butyl 2,3,4,5-tetrahydro-4-[(R)-2-hydroxy-1-phenylethyl]-2-methyl-3-oxobenzo[e][1,4]diazepine-1-carboxylate 
• 855307-27-6 tert-butyl 2,3,4,5-tetrahydro-4-[(R)-2-hydroxy-1-phenylethyl]-3-oxobenzo[e][1,4]diazepine-1-carboxylate 
• 855307-32-3 (R)-1,2,4,5-tetrahydro-4-[(R)-2-hydroxy-1-phenylethyl]-2-methyl-3-oxobenzo[e][1,4]diazepin-3-one 
• 855307-33-4 (R)-2-[(R)-2,3-dihydro-2-methyl-1H-benzo[e][1,4]diazepin-4(5H)-yl]-2-phenylethanol 
• 855307-26-5 tert-butyl 2-[{2-bromo-N-[(R)-2-(tert-butyldiphenylsilyloxy)-1-phenylethyl]acetamido}methyl]phenylcarbamate 

Relevant academic research and scientific papers

An efficient asymmetric synthesis of 2-substituted 1,4-benzodiazepin-3-one as a potential molecular scaffold

2-Substituted 1,4-benzodiazepine-2-one compounds (9-12) were obtained by a highly diastereoselective alkylation of a seven-membered ring benzolactam (8) in the presence of (R)-pbenylglydnol as a chiral inductor. The corresponding add derivative (16) affor