(2S,3S,4S,5S)-1-(tertbutoxycarbonyl)-3,4-bis-(benzyloxy)-2-((benzyloxy)methyl)-5-(3,3-oxobutyl)pyrrolidine

Base Information

Chemical Name:(2S,3S,4S,5S)-1-(tertbutoxycarbonyl)-3,4-bis-(benzyloxy)-2-((benzyloxy)methyl)-5-(3,3-oxobutyl)pyrrolidine
CAS No.:1231217-48-3
Molecular Formula:C₃₅H₄₃NO₆
Molecular Weight:573.73
Hs Code.:

Synonyms:(2S,3S,4S,5S)-1-(tertbutoxycarbonyl)-3,4-bis-(benzyloxy)-2-((benzyloxy)methyl)-5-(3,3-oxobutyl)pyrrolidine

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Chemical Property of (2S,3S,4S,5S)-1-(tertbutoxycarbonyl)-3,4-bis-(benzyloxy)-2-((benzyloxy)methyl)-5-(3,3-oxobutyl)pyrrolidine

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Technology Process of (2S,3S,4S,5S)-1-(tertbutoxycarbonyl)-3,4-bis-(benzyloxy)-2-((benzyloxy)methyl)-5-(3,3-oxobutyl)pyrrolidine

There total 1 articles about (2S,3S,4S,5S)-1-(tertbutoxycarbonyl)-3,4-bis-(benzyloxy)-2-((benzyloxy)methyl)-5-(3,3-oxobutyl)pyrrolidine 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:

: 1231217-57-4
C₃₅H₄₅NO₆

: 1231217-48-3
(2S,3S,4S,5S)-1-(tertbutoxycarbonyl)-3,4-bis-(benzyloxy)-2-((benzyloxy)methyl)-5-(3,3-oxobutyl)pyrrolidine

Guidance literature:: With silica gel; pyridinium chlorochromate; In dichloromethane; at 20 ℃; for 4h;
DOI:10.1055/s-0029-1219540

Reference yield: 87.0%

: 1231217-48-3
(2S,3S,4S,5S)-1-(tertbutoxycarbonyl)-3,4-bis-(benzyloxy)-2-((benzyloxy)methyl)-5-(3,3-oxobutyl)pyrrolidine

: 1231217-53-0
(1S,2S,3S,5S,7aS)-1,2-bis-(benzyloxy)-3-((benzyloxy)methyl)-5-methyl-pyrrolizidine

Guidance literature:: (2S,3S,4S,5S)-1-(tertbutoxycarbonyl)-3,4-bis-(benzyloxy)-2-((benzyloxy)methyl)-5-(3,3-oxobutyl)pyrrolidine; With trifluoroacetic acid; In dichloromethane; at 20 ℃; for 5h;

With sodium tetrahydroborate; In methanol; at 0 ℃; for 0.5h; diastereoselective reaction;
DOI:10.1055/s-0029-1219540