dc.contributor.author | Theodoropoulos, DM | en |
dc.contributor.author | Fruton, JS | en |
dc.date.accessioned | 2014-03-01T01:37:39Z | |
dc.date.available | 2014-03-01T01:37:39Z | |
dc.date.issued | 1962 | en |
dc.identifier.issn | 00062960 | en |
dc.identifier.uri | https://dspace.lib.ntua.gr/xmlui/handle/123456789/21589 | |
dc.relation.uri | http://www.scopus.com/inward/record.url?eid=2-s2.0-33947471972&partnerID=40&md5=c961644e3f67f598a72e3cfd086874eb | en |
dc.subject.other | peptide | en |
dc.subject.other | tryptophan | en |
dc.subject.other | article | en |
dc.subject.other | PEPTIDES | en |
dc.subject.other | TRYPTOPHAN | en |
dc.subject.other | Peptides | en |
dc.subject.other | Tryptophan | en |
dc.title | Synthesis of tryptophan peptides | en |
heal.type | journalArticle | en |
heal.publicationDate | 1962 | en |
heal.abstract | Synthetic methods are described for the synthesis of the p-toluenesulfonates of glycyl-L-tryptophanamide, L-tryptophylglycyl-L-tryptophanamide, and glycyl-L-tryptophylglycyl-L-tryptophanamide. During the course of this work several carbobenzoxy and trityl derivatives of tryptophan peptides were prepared, and the applicability of various coupling methods was examined. Attention is drawn to the possible formation of β-oxyindolylalanine derivatives upon decarbobenzoxylation of protected tryptophan peptides by HBr-acetic acid. © Copyright 1962 by the American Chemical Society. | en |
heal.journalName | Biochemistry | en |
dc.identifier.volume | 1 | en |
dc.identifier.issue | 6 | en |
dc.identifier.spage | 933 | en |
dc.identifier.epage | 937 | en |
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