76905-19-6

Upstream product

• 20445-31-2 R-(+)-α-trifluoromethyl-α-methoxy-phenylacetic acid 
• 66997-66-8 (S)-methyl 3-hydroxydecanoate 
• 1353031-50-1 (S)-1-[(R)-4-benzyl-2-thioxothiazolidin-3-yl]-3-hydroxydecan-1-one 
• 124-13-0 Octanal 
• 19526-23-9 3-(S)-hydroxydecanoic acid 
• 1122101-76-1 (S)-3-(((S)-3-[α-L-rhamnopyranosyl]decanoyl)oxy)decanoic acid 
• 39637-99-5 (S)-(+)-2-methoxy-2-trifluoromethyl-2-phenylacetyl chloride 
• 1420535-14-3 (3S)-3-(6-deoxy-α-L-mannopyranosyloxy)decanoic acid 
• 47767-22-6 (S)-3-(((R)-3-[α-L-rhamnopyranosyl]decanoyl)oxy)decanoic acid 
• 111-64-8 n-octanoic acid chloride 
• 66696-94-4 benzyl 3-oxodecanoate 
• 132016-02-5 benzyl (±)-3-hydroxydecanoate 
• 1420535-13-2 (3S)-3-[(2,3,4-tri-O-acetyl-6-deoxy-α-L-mannopyranosyl)oxy]decanoic acid 
• 1420535-12-1 (3R)-3-[(2,3,4-tri-O-acetyl-6-deoxy-α-L-mannopyranosyl)oxy]decanoic acid 

Relevant academic research and scientific papers

Total Synthesis and Stereochemical Assignment of Sunshinamide and Its Anticancer Activity

Total synthesis of cyclodepsipeptide sunshinamide has been achieved for the first time using a convergent approach. The key features of this synthesis comprise Crimmins acetate aldol, Shiina esterification, amide coupling, macrolactamization, and an Isub

Synthesis and Characterization of Four Diastereomers of Monorhamnolipids

Rhamnolipids are amphiphilic glycolipids biosynthesized by bacteria that, due to their low toxicity and biodegradability, are potential replacements for synthetic surfactants. The previously limited access to pure materials at the gram scale has hindered