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Acyl Azides and the Use of Protected Hydrazides

FIGURE 7.26 Reaction of diphenyl phosphorazidate (DPPA) with a carboxylate anion to give the acyl azide.90 [Pg.226]

K Hofmann, A Lindenmann, MZ Magee, NH Khan. Studies on polypeptides III. Novel routes to a-amino acid and peptide hydrazides. (protected hydrazides). J Am [Pg.226]

J Honzl, J Rudinger. Amino acids and peptides. XXXIII. Nitrosyl chloride and butyl nitrite as reagents in peptide synthesis by the azide method suppression of amide formation. Coll Czech Chem Comm 26, 2333, 1961. [Pg.226]

M Ohno, CB Anfinsen. Removal of protected peptides by hydrazinolysis after synthesis by solid-phase. J Am Chem Soc 89, 5994, 1967. [Pg.226]

L Kisfaludy, O Nyeki. Racemization during peptide azide coupling. Acta ChimAcad Sci Hung 72, 75, 1972. [Pg.226]


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