2.2.2‐Trifluor‐1‐acylamino‐äthyl‐Reste als Schutzgruppen für die Iminogruppe des Histidins bei Peptidsynthesen
- 1 December 1967
- journal article
- research article
- Published by Wiley in European Journal of Inorganic Chemistry
- Vol. 100 (12) , 3841-3849
- https://doi.org/10.1002/cber.19671001205
Abstract
No abstract availableKeywords
This publication has 14 references indexed in Scilit:
- N ‐Acyl‐trihalogenacetaldimine als reaktive Zwischenstufen bei Eliminierungs‐Additions‐Reaktionen, VI. Austausch der Trifluoracetoxygruppe gegen nucleophile Reste bei 2.2.2‐Trifluor‐1‐trifluoracetoxy‐ N ‐acyl‐äthylaminenEuropean Journal of Inorganic Chemistry, 1967
- Adamantyloxycarbonyl, a New Blocking Group. Preparation of 1-Adamantyl Chloroformate1Journal of the American Chemical Society, 1966
- Synthese der Insulinsequenz B 9 — 13European Journal of Organic Chemistry, 1963
- Reactivity of Cyclic Peptides. II. cyclo-L-Tyrosyl-L-histidyl and cyclo-L-Tyrosyltriglycyl-L-histidylglycylJournal of the American Chemical Society, 1962
- On the Trityl Method for Peptide Synthesis1Journal of the American Chemical Society, 1959
- Synthesis of Histidyl PeptidesBulletin of the Chemical Society of Japan, 1958
- A New Synthesis of Histidyl PeptidesNature, 1958
- Carbobenzoxy Derivatives of Histidine, Imidazole and Benzimidazole1Journal of the American Chemical Society, 1957
- The Synthesis of L-Seryl-L-histidyl-L-leucyl-L-valyl- L-glutamic Acid, a Peptide with Strepogenin ActivityJournal of the American Chemical Society, 1956
- Studies on Imidazole Compounds. I. A Synthesis of Imidazoles with Functional Groups in the 2-PositionJournal of the American Chemical Society, 1949