140677-52-7

Upstream product

• 140677-49-2 (S)-ethyl 3-amino-2-oxo-2,3,4,5-tetrahydro-1H-pyrrolo<1,2-b><1,2>diazepine-1-acetate 
• 140696-60-2 (S)-2-((benzyloxycarbonyl)amino)-8,8-(ethylenedioxy)-5-oxooctanoic acid 
• 140677-48-1 (S)-ethyl 6-((benzyloxycarbonyl)(hydroxymethyl)amino)-3-((3,3-ethylenedioxy)propyl)-7-oxo-4,5,6,7-tetrahydro-1H-1,2-diazepine-1-acetate 
• 140677-45-8 (S)-2-((benzyloxcarbonyl)amino)-4-(1-phthalimido-2-pyrrolyl)butanoic acid 
• 140677-44-7 (S)-3-(benzyloxycarbonyl)-4-(6,6-(ethylenedioxy)-3-oxohexyl)oxazolidin-5-one 
• 140677-43-6 (S)-ethyl 3-((benzyloxycarbonyl)amino)-2-oxo-2,3,4,5-tetrahydro-1H-pyrrolo<1,2-b><1,2>diazepine-1-acetate 
• 140677-46-9 (S)-2-((benzyloxycarbonyl)amino)-4-(1-amino-2-pyrrolyl)butanoic acid 
• 140677-47-0 (S)-3((benzyloxycarbonyl)amino)-2,3,4,5-tetrahydro-1H-pyrrolo<1,2-b><1,2>diazepin-2-one 
• 140677-51-6 (3S,1'R)-ethyl-3-((1-(ethoxycarbonyl)-3-phenylpropyl)amino)-2-oxo-2,3,4,5-tetrahydro-1H-pyrrolo<1,2-b><1,2>diazepine-1-acetate 
• 23632-67-9 (S)-3-[3-(benzyloxycarbonyl)-5-oxooxazolidin-4-yl]propanoic acid 
• 58456-26-1 (S)-4-<2'-(Chloroformyl)ethyl>-5-oxooxazolidin-3-carbonsaeure-benzylester 

Relevant academic research and scientific papers

Asymmetric Synthesis of Pyrrolodiazepine Derivatives as Potential Antihypertensive Drugs

The asymmetric synthesis of compound 1, with potential angiotensin-converting enzyme inhibitory activity, is reported.From the chiral precursor 5, readily available from L-glutamic acid, two strategies to the key heterocyclic system pyrrolodia