870192-76-0

Upstream product

• 845521-50-8 N-[(1,1-dimethylethoxy)carbonyl]-L-valyl-L-threonyl-O-(phenylmethyl)-L-serine (1R,2S)-1-[(1S)-2-hydroxy-1-methylethyl]-2-methylhexadecyl ester 
• 870192-69-1 (S)-3-Benzyloxy-2-benzyloxycarbonylamino-propionic acid (2S,3S,4S)-3,5-dihydroxy-2,4-dimethyl-pentyl ester 
• 870192-72-6 (S)-3-Benzyloxy-2-benzyloxycarbonylamino-propionic acid (1S,2S)-3-(tert-butyl-dimethyl-silanyloxy)-2-methyl-1-((R)-1-methyl-2-oxo-ethyl)-propyl ester 
• 870192-71-5 (S)-3-Benzyloxy-2-benzyloxycarbonylamino-propionic acid (1R,2S)-3-(tert-butyl-dimethyl-silanyloxy)-1-((S)-2-hydroxy-1-methyl-ethyl)-2-methyl-propyl ester 
• 870192-74-8 (S)-2-Amino-3-benzyloxy-propionic acid (1R,2S)-1-[(S)-2-(tert-butyl-dimethyl-silanyloxy)-1-methyl-ethyl]-2-methyl-hexadecyl ester 
• 870192-73-7 (S)-3-Benzyloxy-2-benzyloxycarbonylamino-propionic acid (Z)-(1R,2S)-1-[(S)-2-(tert-butyl-dimethyl-silanyloxy)-1-methyl-ethyl]-2-methyl-hexadec-3-enyl ester 
• 870192-75-9 N-[(1,1-dimethylethoxy)carbonyl]-L-valyl-L-threonyl-O-(phenylmethyl)-L-serine (1R,2S)-1-[(1S)-2-[(1,1-dimethylethyl)dimethylsilyl]oxy-1-methylethyl]-2-methylhexadecyl ester 
• 20806-43-3 Z-Ser(Bzl)-OH 

Downstream Products

• 845521-51-9 (2R,3R,4S)-3-{(S)-2-[(2S,3R)-2-((S)-2-Amino-3-methyl-butyrylamino)-3-hydroxy-butyrylamino]-3-benzyloxy-propionyloxy}-2,4-dimethyl-octadecanoic acid 
• 845521-53-1 (3S,6S,9S,12R,13R)-3-Benzyloxymethyl-6-((R)-1-hydroxy-ethyl)-9-isopropyl-12-methyl-13-((S)-1-methyl-pentadecyl)-1-oxa-4,7,10-triaza-cyclotridecane-2,5,8,11-tetraone 

Relevant academic research and scientific papers

Total synthesis of stevastelins B3 and C3: Structure confirmation of stevastelin B3 and revision of stevastelin C3

The total synthesis of stevastelin B3, stevastelin C3 and 5-deoxy derivative of stevastelin C3, novel 13-membered cyclic depsipeptides, is described. This study unambiguously confirmed the proposed absolute structure of stevastelin B3, and revealed that t

Synthesis of [13]-membered macrocyclic stevastelins via a transesterification reaction as the key step: Total synthesis of stevastelin C3

A new synthesis of stevastelin C3 (3), a [13]-membered ring component of the stevastelin family, whose structure was recently revised, is reported. Initially, a macrolactonization approach was attempted to generate the [13]-membered macrolactone but this