Results 121 to 130 of about 2,638 (179)
Some of the next articles are maybe not open access.

ChemInform Abstract: SYNTHESIS OF 5,6‐DIHYDRO‐2‐PYRONE AND 2‐PYRONE

Chemischer Informationsdienst, 1974
AbstractVinylessigsäure (I) reagiert mit Formaldehyd (II) in siedendem Eisessig ′in Gegenwart von konz. Schwefelsäure in bescheidenen Ausbeuten zum 5;6‐Dihydro‐2‐pyron (III), das nach Bromierung mit n‐Bromsuccinimid (V) in Tetrachlorkohlenstoff zu (VI) und Dehydrobromierung mit Triäthylamin 2‐Pyron (VII) ergibt.
M. NAKAGAWA   +4 more
openaire   +1 more source

Phenyl derivatives of 2-pyrone

Chemistry of Heterocyclic Compounds, 1971
Several phenyl dichloropentadienyl ketones containing a hydroxy or methoxy group in the benzene ring as well as a number of 2-pyrones based on them were synthesized. The possibility of the conversion of the latter to the corresponding 2-pyridones on heating them with ammonium salts is demonstrated.
Yu. V. Maevskii, S. V. Sokolovskaya
openaire   +1 more source

A Concise Access to 3-Substituted 2-Pyrones.

The Journal of Organic Chemistry, 2010
The development of a modular synthesis of 3-substituted-2-pyrones is described. The attainment of this strategy hinges on a new electrophilic pyrone derivative which can be readily prepared on a multigram scale and which performs very competently in metal-catalyzed cross-coupling reactions with a variety of nucleophiles.
Frébault, F.   +3 more
openaire   +3 more sources

Preparation of 2-pyrone-5- and 2-pyrone-6-carboxylic acid through ?, ?-dichloroacrolein

Bulletin of the Academy of Sciences of the USSR Division of Chemical Science, 1962
We have carried out the synthesis of 2-pyrone-5- and 2-pyrone-6-carboxylic acids usingβ,β-dichloro-acrolein.
L. I. Zakharkin, L. P. Sorokina
openaire   +1 more source

The 2-pyrones of Aniba species

Phytochemistry, 1971
Abstract A re-examination of the trunk wood of Aniba parviflora (Meissn.) Mez (Lauraceae) yielded two new constituents, 6-(4′-hydroxy- trans -styryl)-2-pyrone (IVf) and 6-(3′,4′-dihydroxy- trans -styryl-2-pyrone (IVe). 6- Cis -styryl-2-pyrone (Va) was also isolated.
Rezende, C. M. Andrade da Mata   +4 more
openaire   +2 more sources

PROGRESS IN THE CHEMISTRY OF 2-PYRONES

Russian Chemical Reviews, 1967
CONTENTS I. Introduction 175 II. Methods of synthesis of 2-pyrones 175 III.
N P Shusherina   +3 more
openaire   +1 more source

2-Pyrones possessing antimicrobial and cytotoxic activities

Bioorganic & Medicinal Chemistry, 2004
The 2-pyrone sub-unit is found in a number of natural products possessing broad spectrum biological activity. Such compounds are validated as being capable of binding to specific protein domains and able to exert a remarkable range of biological effects.
Ian J S, Fairlamb   +4 more
openaire   +2 more sources

Pyridine-2-thiones, 2-pyrone phenylhydrazones, and 2-pyridones from 2-pyrones

Journal of the Chemical Society C: Organic, 1971
Various 5-aryloxypyran-2-thiones, 2-pyridones, and 1-amino-2-pyridones have been prepared. The pyran-2-thiones were converted into pyridine-2-thiones and phenylhydrazones. Some derivatives of 6-p-bromophenyl-5-phenoxy-4-phenyl-2-pyrone (Ia) are described.
openaire   +1 more source

Substituted 2‐Pyrones and 5,6‐Dihydropyrones

Journal of Heterocyclic Chemistry, 1985
AbstractA series of substituted 2‐pyrones and 5,6‐dihydropyrones have been synthesized and investigated for their inhibitory activity toward human leukocyte elastase, procine pancreatic elastase and chymotrypsin.
William C. Groutas   +4 more
openaire   +1 more source

Asymmetric Hydrogenation of Substituted 2-Pyrones

The Journal of Organic Chemistry, 1999
Various substituted 2-pyrones have been hydrogenated with high enantioselectivity (up to 97% ee) to the corresponding 5,6-dihydropyrones using cationic ruthenium catalysts containing the (6,6‘-dimethoxybiphenyl-2,2‘diyl)bis[3,5-di(tert-butyl)phenylphosphine] ligand. When substituents at position 3 are absent, 5,6-dihydropyrones are further hydrogenated
Matthias J. Fehr   +3 more
openaire   +1 more source

Home - About - Disclaimer - Privacy