132402-65-4

Upstream product

• 18598-63-5 L-cysteine methyl ester hydrochloride 
• 132402-58-5 2-allyloxycarbonylamino-3-phenyl-(S)-propioimino ethyl ether 
• 90508-20-6 N-allyloxycarbonyl-(S)-phenylalanate 
• 132402-50-7 (S)-N-(allyloxycarbonyl)phenylalaninamide 
• 1452389-59-1 alloc-L-Phe-L-Cys(Trt)-OMe 
• 128369-71-1 (S)-methyl-(N-allyloxycarbonyl)phenylalaninate 

Downstream Products

• 1452389-54-6 (S)-Phe-(4R)-thiazoline-OH 
• 132402-83-6 (S)-1-((S)-2-{[2-((S)-1-Allyloxycarbonylamino-2-phenyl-ethyl)-thiazole-4-carbonyl]-amino}-3-phenyl-propionyl)-pyrrolidine-2-carboxylic acid tert-butyl ester 
• 132402-80-3 2-<(S)-1-allyloxycarbonylamino-2-phenyl-ethyl>-4-carboxythiazole 
• 132402-73-4 2-<(S)-1-allyloxycarbonylamino-2-phenyl-ethyl>-4-methoxycarbonylthiazole 

Relevant academic research and scientific papers

Total synthesis and stereochemical assignment of baringolin

The thiopeptide antibiotic baringolin has been synthesized, and its structure and stereochemistry have been confirmed. The use of a strategy based on palladium-catalyzed cross-couplings permitted a modular construction of this natural product. Copyright

Synthetic studies towards cyclic peptides. Concise synthesis of thiazoline and thiazole containing amino acids

Concise and efficient syntheses of optically pure thiazoline and thiazole containing amino acids of the constitution (26) and (27), based on simple condensation reactions between cysteine esters and N-protected imino ethers (22) and (25) derived from chir