Synthetic Methods and Reactions. Part 106. Suppression of anchimerically assisted rearrangement products in the synthesis of α‐fluorocarboxylic acids from α‐amino acids with 48:52 (w/w) hydrogen fluoride/pyridine [1]
- 16 December 1981
- journal article
- research article
- Published by Wiley in Helvetica Chimica Acta
- Vol. 64 (8) , 2528-2530
- https://doi.org/10.1002/hlca.19810640806
Abstract
No abstract availableKeywords
This publication has 4 references indexed in Scilit:
- Stereospezifische 1,2‐Wanderungen von Hydroxyl‐, Aryl‐ und Alkyl‐ gruppen bei der Nitrosierung von Aminosäuren in Fluorwasserstoff/Pyridin. Vorläufige mitteilungHelvetica Chimica Acta, 1980
- 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
- Synthetic Methods and Reactions XII1. Preparation of α-Fluorocarboxylic Acids from α-Amino Acids via Diazotization in Polyhydrogen Fluoride/Pyridine Solution.Synthesis, 1974
- Synthetic Methods and Reactions II1. Hydrofluorination of Alkenes, Cyclopropane and Alkynes with Poly-Hydrogen Fluoride/Pyridine (Trialkylamine)ReagentsSynthesis, 1973