Stereospezifische 1,2‐Wanderungen von Hydroxyl‐, Aryl‐ und Alkyl‐ gruppen bei der Nitrosierung von Aminosäuren in Fluorwasserstoff/Pyridin. Vorläufige mitteilung
- 6 June 1980
- journal article
- research article
- Published by Wiley in Helvetica Chimica Acta
- Vol. 63 (4) , 769-772
- https://doi.org/10.1002/hlca.19800630403
Abstract
No abstract availableThis publication has 5 references indexed in Scilit:
- Synthetic methods and reactions. 63. Pyridinium poly(hydrogen fluoride) (30% pyridine-70% hydrogen fluoride): a convenient reagent for organic fluorination reactionsThe Journal of Organic Chemistry, 1979
- Migration of electronegative substituents. I. Relative migratory aptitude and migration tendency of the carbethoxy group in the dienone-phenol rearrangementJournal of the American Chemical Society, 1974
- Synthetic Methods and Reactions XII1. Preparation of α-Fluorocarboxylic Acids from α-Amino Acids via Diazotization in Polyhydrogen Fluoride/Pyridine Solution.Synthesis, 1974
- Atlas of StereochemistryPublished by Springer Nature ,1974
- Examinations on the neighboring aryl group participation in nitrous acid deaminations of l-phenylalanine and its p-nitro and p-methoxy derivatives. Conversion of l-phenylalanine to naturally occurring s-tropic acidTetrahedron Letters, 1971