1034401-95-0

Upstream product

• 1034401-93-8 C₂₃H₃₅NO₆ 
• 6456-74-2 Glycine tert-butyl ester 
• 182193-69-7 (S)-1-(p-methoxybenzyloxy)-2-methylpentan-3-one 
• 1034401-91-6 ((2S,3R,4S)-1-hydroxy-2,4-dimethyldecan-3-yl) (S)-2-(benzyloxycarbonylamino)propanoate 
• 1034401-88-1 ((2S,3R,4S)-1-(tert-butyldimethylsilyloxy)-2,4-dimethyldecan-3-yl) (S)-2-(benzyloxycarbonylamino)propanoate 
• 1034401-86-9 (2S,3R,4S)-1-(tert-butyldimethylsilyloxy)-2,4-dimethyldecan-3-ol 
• 1034401-68-7 (2S,3R,4S)-2,4-dimethyldecane-1,3-diol 
• 1453811-62-5 (2R,3R,4S,5S)-6-(4-methoxybenzyloxy)-3,5-dimethyl-1-(triisopropylsilyloxy)hexane-2,4-diol 
• 496035-36-0 (2R,3S,4S)-3-hydroxy-5-(4-methoxybenzyloxy)-2,4-dimethylpentanal 
• 1453811-59-0 (2S,4S,5R)-5-hydroxy-1-(4-methoxybenzyloxy)-2,4-dimethyl-6 (triisopropylsilyloxy) hexan-3-one 

Relevant academic research and scientific papers

Total synthesis of emericellamides A and B

A concise total synthesis of emericellamides A and B, two cyclic depsipeptides exhibiting antibacterial and cytotoxic activities, is reported. A Paterson anti-aldol reaction and a hydroxy directed 1,3-anti reduction were applied for construction of the po

The first total synthesis of emericellamide A

A highly convergent asymmetric total synthesis of emericellamide A, a 19-membered antibacterial depsipeptide isolated from the co-culture of an Emericella sp. (strain CNL-878) and a Salinispora arenicola (strain CNH-665) is described.