-
Online corrected version: (2006–) "
azlactones". doi:10.1351/goldbook.A00559 K. Mukerjee, Arya (1987). "
Azlactones:
Retrospect and Prospect". Heterocycles...
- The
Bergmann azlactone peptide synthesis is a
classic organic synthesis process for the
preparation of dipeptides. In the
presence of a base, peptides...
- The Erlenmeyer–Plöchl
azlactone and
amino acid synthesis,
named after Friedrich Gustav Carl Emil
Erlenmeyer who
partly discovered the reaction, is a series...
-
stilbene is yet
another product of this methodology. Erlenmeyer–Plöchl
azlactone and amino-acid
synthesis Stobbe condensation Pechmann condensation Perkin...
-
Empire Alma mater
University of Göttingen, (1888) Known for
Erlenmeyer azlactone synthesis Invention of
eosin cell
stain Scientific career Institutions...
-
Enyne metathesis Epoxidation Erlenmeyer synthesis,
Azlactone synthesis Erlenmeyer–Plöchl
azlactone and amino-acid
synthesis Eschenmoser fragmentation...
- Jr., was a
German chemist and the
discoverer of the Erlenmeyer-Plöchl
azlactone and
amino acid synthesis. He was the son of
Richard August Carl Emil Erlenmeyer...
- a
nucleophile for the
cyclization forming the
azlactone 4.
Deprotonation and
acylation of the
azlactone forms the key carbon-carbon bond.
Subsequent ring-opening...
-
phenylalanine and
other amino acids, the
reaction proceeding via an
oxazolone or "
azlactone" intermediate.
Justus von
Liebig showed in 1829 that
hippuric acid differed...
-
Richard S.; Breitholle,
Edward G.; Stammer,
Charles H. (March 1980). "
Azlactone oxidation". The
Journal of
Organic Chemistry. 45 (6): 1151–1153. doi:10...
