<(2'R,3'S,4'S)-3'-Acetamido-4'-(benzyloxy)-2'-<(1''S,2''R)-1'',2'',3''-tris(benzyloxy)propyl>pyrrolidin-1'-yl>oxoacetic acid

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Chemical Name:<(2'R,3'S,4'S)-3'-Acetamido-4'-(benzyloxy)-2'-<(1''S,2''R)-1'',2'',3''-tris(benzyloxy)propyl>pyrrolidin-1'-yl>oxoacetic acid
CAS No.:131292-87-0
Molecular Formula:C₃₉H₄₂N₂O₈
Molecular Weight:666.771
Hs Code.:

Synonyms:<(2'R,3'S,4'S)-3'-Acetamido-4'-(benzyloxy)-2'-<(1''S,2''R)-1'',2'',3''-tris(benzyloxy)propyl>pyrrolidin-1'-yl>oxoacetic acid

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Chemical Property of <(2'R,3'S,4'S)-3'-Acetamido-4'-(benzyloxy)-2'-<(1''S,2''R)-1'',2'',3''-tris(benzyloxy)propyl>pyrrolidin-1'-yl>oxoacetic acid

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Technology Process of <(2'R,3'S,4'S)-3'-Acetamido-4'-(benzyloxy)-2'-<(1''S,2''R)-1'',2'',3''-tris(benzyloxy)propyl>pyrrolidin-1'-yl>oxoacetic acid

There total 2 articles about <(2'R,3'S,4'S)-3'-Acetamido-4'-(benzyloxy)-2'-<(1''S,2''R)-1'',2'',3''-tris(benzyloxy)propyl>pyrrolidin-1'-yl>oxoacetic acid which guide to synthetic route it. The literature collected by LookChem mainly comes from the sharing of users and the free literature resources found by Internet computing technology. We keep the original model of the professional version of literature to make it easier and faster for users to retrieve and use. At the same time, we analyze and calculate the most feasible synthesis route with the highest yield for your reference as below:

synthetic route:

Reference yield: 75.0%

: 131292-86-9
Methyl <(2'R,3'S,4'S)-3'-Acetamido-4'-(benzyloxy)-2'-<(1''S,2''R)-1'',2'',3''-tris(benzyloxy)propyl>pyrrolidin-1'-yl>oxoacetate

: 131292-87-0
<(2'R,3'S,4'S)-3'-Acetamido-4'-(benzyloxy)-2'-<(1''S,2''R)-1'',2'',3''-tris(benzyloxy)propyl>pyrrolidin-1'-yl>oxoacetic acid

Guidance literature:: With sodium hydroxide; In methanol; for 2h; Ambient temperature;
DOI:10.1002/hlca.19900730522

Reference yield:

: C₃₇H₄₂N₂O₅*BH₃*ClH

: 131292-87-0
<(2'R,3'S,4'S)-3'-Acetamido-4'-(benzyloxy)-2'-<(1''S,2''R)-1'',2'',3''-tris(benzyloxy)propyl>pyrrolidin-1'-yl>oxoacetic acid

Guidance literature:: Multi-step reaction with 2 steps

1: 70 percent / Et₃N / CH₂Cl₂ / Ambient temperature

2: 75 percent / 2M NaOH / methanol / 2 h / Ambient temperature

With sodium hydroxide; triethylamine; In methanol; dichloromethane;
DOI:10.1002/hlca.19900730522