Reactions · Organic Syntheses ↗
Discussion Addendum for: (Oxidation of Nerol to Neral with Iodosobenzene and TEMPO)
Oxidation
Overview
Preparation of Oxidation of Nerol to Neral with Iodosobenzene and TEMPO. Submitted by Francesca Leonelli1a, Roberto Margarita1b, and Giovanni Piancatelli*1c. DOI: 10.15227/orgsyn.089.0311.
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