125782-38-9

Upstream product

• 5927-18-4 trimethyl phosphonoacetate 
• 79026-61-2 (R)-3-benzyloxy-2-methylpropanal 
• 88738-78-7 bis-(2,2,2-trifluoroethyl)(methoxycarbonylmethyl)phosphonate 
• 63930-46-1 (S)-3-benzyloxy-2-methylpropan-1-ol 

Downstream Products

• 114762-43-5 (4S,2Z)-5-(benzyloxy)-4-methyl-2-penten-1-ol 
• 125782-36-7 (2S,3R,4R)-5-(benzyloxy)-3-hydroxy-4-methyl-2-(methylamino)pentanoic acid 
• 125782-40-3 (1'R,4R,5R)-5-<2'-(benzyloxy)-1'-methylethyl>-4-(hydroxymethyl)-3-methyl-2-oxazolidinone 
• 125782-39-0 (2S,3R,4R)-5-(benzyloxy)-2,3-epoxy-4-methyl-1-<(N-methylcarbamoyl)oxy>pentane 
• 125782-52-7 (4S,5R)-5-((R)-2-Benzyloxy-1-methyl-ethyl)-2,2,3-trimethyl-oxazolidine-4-carboxylic acid 
• 125782-41-4 (1'R,4S,5R)-5-<2'-(benzyloxy)-1'-methylethyl>-3-methyl-2-oxooxazolidine-4-carboxylic acid 
• 125782-37-8 (2S,3R,4R)-5-<(4'-benzoylbenzyl)oxy>-3-hydroxy-4-methyl-2-(methylamino)pentanoic acid 
• 125782-45-8 (1'R,4R,5R)-5-<2'-<(4''-benzoylbenzyl)oxy>-1'-methylethyl>-4-(hydroxymethyl)-3-methyl-2-oxazolidinone 
• 125782-48-1 (1'R,4S,5R)-5-<2'-<(4''-benzoylbenzyl)oxy>-1'-methylethyl>-3-methyl-2-oxooxazolidine-4-carboxylic acid 
• 125782-56-1 C₄₄H₇₅N₇O₁₀ 
• 125782-57-2 C₄₅H₇₇N₇O₁₀ 
• 125782-53-8 C₄₇H₇₉N₇O₁₀ 
• 125801-24-3 C₄₈H₈₁N₇O₁₀ 
• 125782-59-4 <(2S,3R,4R)-5-(benzyloxy)-3-hydroxy-4-methyl-2-(methylamino)pentanoyl>-L-2-aminobutyryl-sarcosyl-N-methyl-L-leucyl-L-valyl-N-methyl-L-leucyl-L-alanine benzyl ester 

Relevant academic research and scientific papers

Highly stereoselective synthesis of mupirocin H

A highly diastereoselective and efficient convergent synthesis of mupirocin H starting from (+)-(R)-Roche ester was achieved. Grubbs cross metathesis was employed as the key step in the pathway to generate an important E-olefin intermediate. Other process

Synthesis, conformation, and immunosuppressive activity of cyclosporines that contain ε-oxygen (4R)-4-[(E)-butenyl]-4,N-dimethyl-L-threonine analogues in the 1-position

A series of CsA analogues that contain novel ε-oxygen isosteres of (4R)-4-[(E)-butenyl]-4,N-dimethyl-L-threonine (MeBmt) in the 1-position were synthesized. The key steps for the syntheses of enantiomerically pure ε-oxygen MeBmt analogues 4-7 were based o