A new enantioselective synthesis of (4S, 5S)-5-(N-Boc)-amino-6-cyclohexyl-4-hydroxy-hexanoic acid lactone, a hydroxyethylene dipeptide isostere precursor
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Add time:07/18/2019 Source:sciencedirect.com
A new enantioselective synthesis of a valuable hydroxyethylene dipeptide isostere precursor, (4S, 5S)-5-5(N-Boc)-amino-6-cyclohexyl-4-hydroxy-hexanoic acid lactone, has been developed by using coupling reaction of chiral triflates as a key step.
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Prev:Quantitation of 4-cyclohexyl-2-hydroxyl-3-(3-methylsulfanyl-2-{2- [(morpholine-4-carbonyl)amino]-3- phenylpropionylamino}propionylamino)butyric acid isopropyl ester (CP-80, 794), a renin inhibitor, and its hydrolytic cleavage metabolite 2-[(morphine-4-carbonyl)amino]-3-phenylpropionic acid (CP-84,364) in dog and human plasma by high-performance liquid chromatography
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