79432-19-2

Upstream product

• 1145-80-8 N-(benzyloxycarbonyl)-L-serine 
• 16874-17-2 L-phenylalanine tert-butyl ester 
• 25529-31-1 pentafluorophenyl ester of benzyloxycarbonylserine 

Downstream Products

• 79432-20-5 H-Ser-Phe-OBu^t 
• 79432-27-2 Z-Glu(OBu^t)-Gln-Lys(Boc)-Tyr-Ser-Phe-OBu^t 
• 79432-30-7 H-Glu(OBu^t)-Gln-Lys(Boc)-Tyr-Ser-Phe-OBu^t 
• 79432-25-0 Z-Gln-Lys(Boc)-Tyr-Ser-Phe-OBu^t 
• 79432-61-4 H-Glu-Gln-Lys-Tyr-Ser-Phe-OH 
• 79432-23-8 Z-Lys(Boc)-Tyr-Ser-Phe-OBu^t 
• 79432-26-1 H-Gln-Lys(Boc)-Tyr-Ser-Phe-OBu^t 
• 79432-24-9 H-Lys(Boc)-Tyr-Ser-Phe-OBu^t 
• 79432-21-6 Z-Tyr(Bzl)-Ser-Phe-OBu^t 
• 79432-22-7 H-Tyr-Ser-Phe-OBu^t 

Relevant academic research and scientific papers

Chemoselective catalytic conjugate addition of alcohols over amines

A highly chemoselective conjugate addition of alcohols in the presence of amines is described. The cooperative nature of the catalyst enabled chemoselective activation of alcohols over amines, allowing the conjugate addition to soft Lewis basic α,β-unsaturated nitriles. Divergent transformation of the nitrile functionality highlights the utility of the present catalysis. The cooperative nature of a copper catalyst enabled the highly chemoselective activation of alcohols in the presence of amines and thus the conjugate addition of the hydroxy group to soft Lewis basic α,β-unsaturated nitriles. The presented method proceeds under proton-transfer conditions, reverses the innate reactivity of the OH and NH groups, and does not require protecting groups. dppe=1,2-bis(diphenylphosphino) ethane, MeSal=3-methylsalicylate. Copyright

Synthesis of Human Growth Hormone-(27-44)-octadecapeptide and some Smaller Fragment Peptides

Synthesis in solution of human growth hormone-(27-44)-octadecapeptide and a series of smaller fragments was carried out by a stepwise procedure, starting at the carboxy-terminus and utilizing active esters in the acylation reactions.