Eine bequeme Methode zur Herstellung von 1‐(tert‐Butoxycarbonyl)pyrrolen
- 1 April 1984
- journal article
- zuschrift
- Published by Wiley in Angewandte Chemie
- Vol. 96 (4), 291-292
- https://doi.org/10.1002/ange.19840960410
Abstract
No abstract availableKeywords
This publication has 12 references indexed in Scilit:
- Synthesis and antiviral activity of distamycin A analogs: substitutions on the different pyrrole nitrogens and in the amidine functionJournal of Medicinal Chemistry, 1983
- PROTECTION OF THE TRYPTOPHAN INDOLE RING IN PEPTIDE SYNTHESIS. USE OF A NEW DERIVATIVE, Nin-2,2,2-TRICHLOROETHOXYCARBONYLTRYPTOPHANChemistry Letters, 1983
- 4-Dialkylaminopyridines: super acylation and alkylation catalystsChemical Society Reviews, 1983
- Synthesis and reactions of N-protected 2-lithiated pyrroles and indoles. The tert-butoxycarbonyl substituent as a protecting groupThe Journal of Organic Chemistry, 1981
- N‐Acetylierung substituierter PyrroleEuropean Journal of Inorganic Chemistry, 1980
- 4-Dialkylaminopyridine als hochwirksame AcylierungskatalysatorenAngewandte Chemie, 1978
- Verbesserte Herstellung vont-Butoxycarbonyl-fluorid und dessen Verwendung zur Synthese von 1-Boc-3-for-mylindol, einem neuen Reagenz zur Verknüpfung von Peptid-FragmentenSynthesis, 1975
- 4‐Dimethylamino‐pyridin, ein hochwirksamer AcylierungskatalysatorAngewandte Chemie, 1969
- N,N‐Dimethyl‐4‐pyridinamine, a Very Effective Acylation CatalystAngewandte Chemie-International Edition, 1969
- Structure and Synthesis of Distamycin ANature, 1964