170552-57-5

Upstream product

• 170300-08-0 (1S,3S,2'S)-1-<2'-benzyloxycarbonyl-2'-(benzyloxycarbonyl)amino>ethyl-3-methoxycarbonyl-1,2,3,4-tetrahydro-β-carboline 
• 170300-17-1 (2S,5S,11bS)-2-(benzyloxycarbonyl)amino-5-methoxycarbonyl-3-oxo-2,3,5,6,11,11b-hexahydro-1H-indolizino<8,7-b>indole 
• 170552-54-2 (2S,5S,11bR)-2-(benzyloxycarbonyl)amino-5-methoxycarbonyl-3-oxo-2,3,5,6,11,11b-hexahydro-1H-indolizino<8,7-b>indole 

Downstream Products

• 305322-33-2 (S)-2-[((2S,5S,11bR)-2-Benzyloxycarbonylamino-3-oxo-2,3,5,6,11,11b-hexahydro-1H-indolizino[8,7-b]indole-5-carbonyl)-amino]-3-phenyl-propionic acid methyl ester 
• 305322-47-8 [(2S,5S,11bR)-5-((R)-1-Carbamoyl-2-phenyl-ethylcarbamoyl)-3-oxo-2,3,5,6,11,11b-hexahydro-1H-indolizino[8,7-b]indol-2-yl]-carbamic acid benzyl ester 
• 305322-34-3 (R)-2-[((2S,5S,11bR)-2-Benzyloxycarbonylamino-3-oxo-2,3,5,6,11,11b-hexahydro-1H-indolizino[8,7-b]indole-5-carbonyl)-amino]-3-phenyl-propionic acid methyl ester 

Relevant academic research and scientific papers

2-Amino-3-oxohexahydroindolizinoindole-5-carboxylate Derivatives as New Scaffolds for Mimicking β-Turn Secondary Structures. Molecular Dynamics and Stereoselective Synthesis

Highly constrained 2-amino-3-oxohexahydroindolizinoindole-5-carboxylate derivatives of general formula 1 have been developed as novel β-turn mimetics.Molecular dynamics studies on model structures 2a and 2b have revealed that both indolizinoindole

2(S)-amino-3-oxo-11b(R)-hexahydroindolizino[8,7-b]indole-5(S)-carboxylate as a new type of β-turn dipeptide mimetic

Molecular-modelling studies have shown that 2(S)-amino-3-oxo-11 b(R)-hexahydroindolizino[8,7-b]indole- 5(S)-carboxylate, stereoselectively prepared by Pictet-Spengler reaction between H-Trp-OMe and Z-Asp(H)-OBz and subsequent γ-lactamization, behaves as a