1412893-38-9

Upstream product

• 19790-60-4 3-Benzyloxypropanal 
• 787552-67-4 (S)-4-benzyl-3-((2S,3R)-5-benzyloxy-3-hydroxy-2-methylpentanoyl)-2-oxazolidinone 
• 135799-65-4 (2R,3R)-5-Benzyloxy-3-(tert-butyl-dimethyl-silanyloxy)-2-methyl-pentan-1-ol 
• 4530-20-5 BOC-glycine 
• 13139-15-6 N-tert-butoxycarbonyl-L-leucine 
• 28334-73-8 (2S)-2-[[2-(tert-butoxycarbonylamino)acetyl]amino]-3-methylbutanoic acid 
• 1412893-46-9 C₂₂H₄₀N₄O₇ 
• 1412893-47-0 C₂₁H₃₈N₄O₇ 
• 4070-48-8 L-Valine methyl ester 
• 1416567-75-3 C₂₉H₄₁NO₅Si 
• 135799-66-5 (2S,3R)-5-(benzyloxy)-3-((tert-butyldimethylsilyl)oxy)-2-methylpentanal 
• 870091-89-7 (-)-(R)-4-benzyl-3-[(2R,3S)-5-(benzyloxy)-3-hydroxy-2-methylpentanoyl]-1,3-oxazolidin-2-one 
• 872369-15-8 (-)-(R)-4-benzyl-3-[(2R,3S)-5-(benzyloxy)-3-(tert-butyldimethylsilyloxy)-2-methylpentanoyl]-1,3-oxazolidin-2-one 
• 872369-16-9 (?)-(2S,3S)-5-(benzyloxy)-3-(tert-butyldimethylsilyloxy)-2-methylpentan-1-ol 

Downstream Products

• 1202022-06-7 (28R,29R)-arenamide A 
• 1412893-35-6 C₃₆H₅₉N₅O₈ 

Relevant academic research and scientific papers

Total syntheses of 28,29-diepi-arenamide A, 29-epi-arenamide A, and 28-epi-arenamide A

This communication describes the synthesis of stereochemical analogs of arenamide A, a 19-membered cytotoxic depsipeptide isolated from the fermentation broth of a marine bacterial strain Salinispora arenicola. The key steps are diastereoselective aldol r