37813-19-7

Upstream product

• 7635-36-1 Z-Asp(tBu)-OCp 
• 80647-32-1 [(S)-2-((S)-2-{(S)-2-[(2S,3R)-2-((2S,3S)-2-Amino-3-methyl-pentanoylamino)-3-tert-butoxy-butyrylamino]-propionylamino}-3-tert-butoxy-propionylamino)-3-methyl-butyrylamino]-acetic acid phenyl ester; hydrochloride 
• 1676-75-1 N-benzyloxycarbonyl-O-t-butyl-L-serine 
• 3065-23-4 Z-Val-OCp 
• 55878-21-2 glycine phenyl ester hydrobromide 
• 80647-19-4 Z-Val-Gly-OPh 
• 80647-20-7 Z-Ser(tBu)-Val-Gly-OPh 
• 80647-29-6 [(S)-2-((S)-2-Amino-3-tert-butoxy-propionylamino)-3-methyl-butyrylamino]-acetic acid phenyl ester; hydrochloride 
• 80647-21-8 Z-Ala-Ser(tBu)-Val-Gly-OPh 
• 80647-30-9 {(S)-2-[(S)-2-((S)-2-Amino-propionylamino)-3-tert-butoxy-propionylamino]-3-methyl-butyrylamino}-acetic acid phenyl ester; hydrochloride 
• 80647-31-0 ((S)-2-{(S)-2-[(S)-2-((2S,3R)-2-Amino-3-tert-butoxy-butyrylamino)-propionylamino]-3-tert-butoxy-propionylamino}-3-methyl-butyrylamino)-acetic acid phenyl ester; hydrochloride 
• 80647-23-0 Z-Ile-Thr(But)-Ala-Ser(tBu)-Val-Gly-OPh 

Relevant academic research and scientific papers

PEPTIDES-XXXXII. SYNTHESIS OF THE 76-93 FRAGMENT OF A LYSOZYME ANALOGUE

The synthesis of the (76-93) fragment of a lysozyme analogue was achieved using a fragment condensation approach employing the protected subfragments (76-79), (80-86), and (87-93).The utility of Bates'reagent in conjunction with N-hydroxysuccinimide was e