Viel Glück Toxizität Fünfte dess martin periodinane oxidation mechanism leidenschaftlich deutlich Straße
Dess–Martin periodinane - Wikipedia
PDF) Diethylamine Dess-Martin periodinane: An efficient catalyst-oxidant combination in a sequential, one-pot synthesis of difficult to access 2-amino-3,5-dicarbonitrile-6-sulfanylpyridines at ambient temperature
Dess-Martin Oxidation | Chem-Station Int. Ed.
Dess-Martin Oxidation | TCI EUROPE N.V.
Dess–Martin Periodinane | Sigma-Aldrich
Supplemental Topics
Dess-Martin Periodinane - an overview | ScienceDirect Topics
Dess–Martin periodinane oxidative rearrangement for preparation of α-keto thioesters - Organic & Biomolecular Chemistry (RSC Publishing) DOI:10.1039/C7OB02959D
Dess-Martin Oxidation)
Dess–Martin oxidation - Wikipedia
Aldehydes from oxidation of primary alcohols using the Dess- Martin periodinane reagent 14.2 Preparing Aldehydes and Ketones. - ppt download
DM Tutorial
CHEM 222: Dess-Martin Periodinane Oxidation of Alcohols - YouTube
Dess-Martin Periodinane - an overview | ScienceDirect Topics
Dess−Martin Periodinane Oxidation | SpringerLink
Dess-Martin Oxidation - an overview | ScienceDirect Topics
Table 2 from Iodine(V) reagents in organic synthesis. Part 1. Synthesis of polycyclic heterocycles via Dess-Martin periodinane-mediated cascade cyclization: generality, scope, and mechanism of the reaction. | Semantic Scholar