Acetic acid (2S,3S,4S)-4-acetoxy-2-[(1S,2R)-1-benzyloxycarbonylamino-2-(tert-butyl-diphenyl-silanyloxy)-propyl]-3,4-dihydro-2H-pyran-3-yl ester

Base Information

Chemical Name:Acetic acid (2S,3S,4S)-4-acetoxy-2-[(1S,2R)-1-benzyloxycarbonylamino-2-(tert-butyl-diphenyl-silanyloxy)-propyl]-3,4-dihydro-2H-pyran-3-yl ester
CAS No.:131057-60-8
Molecular Formula:C₃₆H₄₃NO₈Si
Molecular Weight:645.825
Hs Code.:

Acetic acid (2S,3S,4S)-4-acetoxy-2-[(1S,2R)-1-benzyloxycarbonylamino-2-(tert-butyl-diphenyl-silanyloxy)-propyl]-3,4-dihydro-2H-pyran-3-yl ester

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Chemical Property of Acetic acid (2S,3S,4S)-4-acetoxy-2-[(1S,2R)-1-benzyloxycarbonylamino-2-(tert-butyl-diphenyl-silanyloxy)-propyl]-3,4-dihydro-2H-pyran-3-yl ester

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Technology Process of Acetic acid (2S,3S,4S)-4-acetoxy-2-[(1S,2R)-1-benzyloxycarbonylamino-2-(tert-butyl-diphenyl-silanyloxy)-propyl]-3,4-dihydro-2H-pyran-3-yl ester

There total 1 articles about Acetic acid (2S,3S,4S)-4-acetoxy-2-[(1S,2R)-1-benzyloxycarbonylamino-2-(tert-butyl-diphenyl-silanyloxy)-propyl]-3,4-dihydro-2H-pyran-3-yl ester 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:

: 108-24-7
acetic anhydride

: 91861-07-3
1-benzoyloxy-2-tert-butyldimethylsilyloxy-4-methoxybuta-1,3-diene

: 131057-58-4
N-carbobenzoxy-O-tert-butyldiphenylsilyl-D-allo-threoninal

: Acetic acid (2S,3R,4S)-4-acetoxy-2-[(1S,2R)-1-benzyloxycarbonylamino-2-(tert-butyl-diphenyl-silanyloxy)-propyl]-3,4-dihydro-2H-pyran-3-yl ester

: 131057-60-8,131102-39-1,134002-79-2
Acetic acid (2S,3S,4S)-4-acetoxy-2-[(1S,2R)-1-benzyloxycarbonylamino-2-(tert-butyl-diphenyl-silanyloxy)-propyl]-3,4-dihydro-2H-pyran-3-yl ester

Guidance literature:: Yield given. Multistep reaction. Yields of byproduct given;
DOI:10.1016/S0040-4020(01)80942-X

Reference yield:

: 131057-60-8,131102-39-1,134002-79-2
Acetic acid (2S,3S,4S)-4-acetoxy-2-[(1S,2R)-1-benzyloxycarbonylamino-2-(tert-butyl-diphenyl-silanyloxy)-propyl]-3,4-dihydro-2H-pyran-3-yl ester

: Acetic acid (2S,3R,4R,5S,6S)-4,5-diacetoxy-2-((1R,2R)-1-benzyloxycarbonylamino-2-hydroxy-propyl)-6-methoxy-tetrahydro-pyran-3-yl ester

Guidance literature:: Multi-step reaction with 3 steps

1: m-chloroperbenzoic acid / 168 h / Ambient temperature

2: triethylamine, DMAP / CH₂Cl₂ / 0.5 h / Ambient temperature

3: H₂ / 10percent Pd/C / methanol / 1 h

With dmap; hydrogen; triethylamine; 3-chloro-benzenecarboperoxoic acid; palladium on activated charcoal; In methanol; dichloromethane;

Reference yield:

: 131057-60-8,131102-39-1,134002-79-2
Acetic acid (2S,3S,4S)-4-acetoxy-2-[(1S,2R)-1-benzyloxycarbonylamino-2-(tert-butyl-diphenyl-silanyloxy)-propyl]-3,4-dihydro-2H-pyran-3-yl ester

: Acetic acid (2S,3R,4R,5S,6S)-4,5-diacetoxy-2-((1R,2R)-2-acetoxy-1-benzyloxycarbonylamino-propyl)-6-methoxy-tetrahydro-pyran-3-yl ester

Guidance literature:: Multi-step reaction with 4 steps

1: m-chloroperbenzoic acid / 168 h / Ambient temperature

2: triethylamine, DMAP / CH₂Cl₂ / 0.5 h / Ambient temperature

3: H₂ / 10percent Pd/C / methanol / 1 h

4: triethylamine, DMAP / CH₂Cl₂ / 0.5 h / Ambient temperature

With dmap; hydrogen; triethylamine; 3-chloro-benzenecarboperoxoic acid; palladium on activated charcoal; In methanol; dichloromethane;