Reactions · Organic Syntheses
CONVERSION OF NITRO TO CARBONYL BY OZONOLYSIS OF NITRONATES: 2,5-HEPTANEDIONE
Oxidation
Overview
Preparation of CONVERSION OF NITRO TO CARBONYL BY OZONOLYSIS OF NITRONATES: 2,5-HEPTANEDIONE. Submitted by John E. McMurry1 and Jack Melton. DOI: 10.15227/orgsyn.056.0036.
Actions
- This entry doesn't have stoichiometric equivalents on file yet — the Reaction Scale Calculator needs at least one participant tagged with an equivalents value.
- Mechanism / source ↗
- View as JSON ↗
Search literature
More Oxidation reactions
- 2-Iodoxy-5-Methylbenzenesulfonic Acid-Catalyzed Selective Oxidation of 4-Bromobenzyl Alcohol to 4-Bromobenzaldehyde or 4-Bromobenzoic Acid with Oxone Oxidation
- A GENERAL SYNTHETIC METHOD FOR THE OXIDATION OF PRIMARY ALCOHOLS TO ALDEHYDES: (S)-(+)-2-METHYLBUTANAL (Butanal, 2-methyl-, (S)-) Oxidation
- Air Oxidation of Primary Alcohols Catalyzed by Copper(I)/TEMPO. Preparation of 2-Amino-5-bromobenzaldehyde Oxidation
- Albright–Goldman oxidation Oxidation
- ALDEHYDES BY OXIDATION OF TERMINAL OLEFINS WITH CHROMYL CHLORIDE: 2,4,4-TRIMETHYLPENTANAL (Pentanal, 2,4,4-trimethyl-) Oxidation
- ALDEHYDES FROM PRIMARY ALCOHOLS BY OXIDATION WITH CHROMIUM TRIOXIDE: HEPTANAL Oxidation