Active Esters and the Strategy of Peptide Synthesis
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Publisher
Springer US
Link
http://link.springer.com/content/pdf/10.1007/978-1-4613-4571-8_2.pdf
Reference145 articles.
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2. Anderson, G. W., Zimmerman, J. E., and Callahan, F. M., 1964, The use of Esters of Nhydroxysuccinimide in peptide synthesis, J. Am. Chem. Soc. 86: 1839.
3. Anderson, G. W., Zimmerman, J. E., and Callahan, F. M., 1966, Racemization control in the synthesis of peptides by the mixed carbonic-carboxylic anhydride method, J. Am. Chem. Soc. 88: 1338.
4. Arens, J. F., 1955, The chemistry of acetylenic ethers. XIII. Acetylenic ethers as reagents for the preparation of amides, Rec. Trau. Chim. 74: 769.
5. Barth, A., and Losse, G., 1964, Darstellung N-geschützter Aminosäure-4-(phenylazo)-phenylester und ihre Verwendung als farbige carboxylaktivierte Verbindungen zur Peptidsynthese, Z. Naturforsch. 196: 264.
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