Über die Stereochemie der Hydrogenolyse von N‐Benzyl‐Bindungen I. Die Hydrogenolyse von Derivaten der 2‐Amino‐2‐phenyl‐propionsäure.
- 1 January 1970
- journal article
- Published by Wiley in Helvetica Chimica Acta
- Vol. 53 (6) , 1370-1378
- https://doi.org/10.1002/hlca.19700530616
Abstract
No abstract availableKeywords
This publication has 28 references indexed in Scilit:
- Studies on Optically Active Amino Acids. XIV. Studies on α-Alkyl-α-amino acids. VII. Determination of Absolute Configuration of Optically Active α-Methylphenylglycine Configuration of Optically Active α-Methylphenylglycine and 1-Methyl-1-phenylpropylamine.CHEMICAL & PHARMACEUTICAL BULLETIN, 1967
- The Absolute Configuration of Optically Active IsovalineCHEMICAL & PHARMACEUTICAL BULLETIN, 1964
- The Stereochemistry of Raney Nickel Action. VI. Functional Group Hydrogenolyses in the α-Substituted α-Phenylpropionic Acid SeriesJournal of the American Chemical Society, 1956
- Studies in Stereochemistry. XIII. The 1,2-Diphenyl-1-propanol SystemJournal of the American Chemical Society, 1952
- The Stereochemistry of Raney Nickel Action. III. The Stereochemical Course of Dehydroxylations in the Benzyl Alcohol SeriesJournal of the American Chemical Society, 1952
- The Problem of the Configurations of Hydratropic Acid and Atrolactic Acid. Application of the Method of Melting Point—Composition DiagramsJournal of the American Chemical Society, 1952
- The Mechanism of Halide Reductions with Lithium Aluminum Hydride. II. Reduction of 2-Chloro-2-phenylpropionic Acid1,2Journal of the American Chemical Society, 1952
- Stereochemical Paths of Reductive DesulfurationJournal of the American Chemical Society, 1952
- Gesetzmäßigkeiten bei der hydrierenden Spaltung von N ‐Benzyl‐VerbindungenBerichte der deutschen chemischen Gesellschaft (A and B Series), 1942
- The Common Basis of Intramolecular Rearrangements. V.1 Inversion of Configuration in Semipinacolic Deamination. The Configurational Relationship between (+)-Alanine and (+)-Methylphenylacetic AcidJournal of the American Chemical Society, 1939