Ester von N‐(9‐Fluorenylmethyloxycarbonyl)aminosäuren mit 4‐Hydroxy‐3‐oxo‐2,5‐diphenyl‐2,3‐dihydrothiophen‐1,1‐dioxid (Fmoc‐Aminosäure‐TDO‐ester) und ihre Verwendung zur Festphasenpeptidsynthese
- 13 May 1988
- journal article
- Published by Wiley in European Journal of Organic Chemistry
- Vol. 1988 (5) , 437-440
- https://doi.org/10.1002/jlac.198819880511
Abstract
No abstract availableKeywords
This publication has 13 references indexed in Scilit:
- Synthesis ofN-2,2,2-(Trichloroethoxycarbonyl)-L-amino Acids andN-(9-Fluorenylmethoxycarbonyl)-L-amino Acids Involving Succinimidoxy Anion as a Leaving Group in Amino Acid ProtectionSynthesis, 1983
- Introduction of 9-fluorenylmethyloxycarbonyl, trichloroethoxycarbonyl, and benzyloxycarbonyl amine protecting groups into O-unprotected hydroxyamino acids using succinimidyl carbonatesCanadian Journal of Chemistry, 1982
- Improved synthesis of 4-alkoxybenzyl alcohol resinThe Journal of Organic Chemistry, 1981
- SOLID‐PHASE PEPTIDE SYNTHESIS USING MILD BASE CLEAVAGE OF NαFLUORENYLMETHYLOXYCARBONYLAMINO ACIDS, EXEMPLIFIED BY A SYNTHESIS OF DIHYDROSOMATOSTATINInternational Journal of Peptide and Protein Research, 1978
- 4,6‐Diphenyl‐thieno[3,4‐d][1,3]dioxol‐2‐on‐5,5‐dioxid, ein neuartiges Aktivierungsmittel für PeptidsynthesenAngewandte Chemie, 1976
- 4,6‐Diphenylthieno [3,4‐d][1,3]dioxol‐2‐one 5,5‐Dioxide, A Novel Activating Agent for Peptide SynthesesAngewandte Chemie International Edition in English, 1976
- Correction. The 9-Fluorenylmethoxycarbonyl Amino-Protecting GroupThe Journal of Organic Chemistry, 1973
- p-Alkoxybenzyl Alcohol Resin and p-Alkoxybenzyloxycarbonylhydrazide Resin for Solid Phase Synthesis of Protected Peptide FragmentsJournal of the American Chemical Society, 1973
- 9-Fluorenylmethoxycarbonyl amino-protecting groupThe Journal of Organic Chemistry, 1972
- 9-Fluorenylmethoxycarbonyl function, a new base-sensitive amino-protecting groupJournal of the American Chemical Society, 1970