𝔖 Bobbio Scriptorium
✦   LIBER   ✦

Oxidations of some α-amino acids under mitsunobu reaction conditions

✍ Scribed by Teodozyj Kolasa; Marvin J. Miller

Publisher
Elsevier Science
Year
1988
Tongue
French
Weight
258 KB
Volume
29
Category
Article
ISSN
0040-4039

No coin nor oath required. For personal study only.

📜 SIMILAR VOLUMES

Regiospecific O-alkylation of δ-tetronic
Regiospecific O-alkylation of δ-tetronic acids under mitsunobu-reaction conditions
✍ Joginder S Bajwa; Robert C Anderson 📂 Article 📅 1990 🏛 Elsevier Science 🌐 French ⚖ 195 KB

An improved procedure for regiospecific 0-alkylation of b-tetronic acids with primary and secondary alcohols, based upon Mitsunobu conditions, is presented. The reaction conditions are very mild and compatible with a variety of hydroxyl protecting groups such as MOM, t-BuMezSi, isopropylidine and es

ChemInform Abstract: The Mitsunobu React
ChemInform Abstract: The Mitsunobu Reaction in the Synthesis of α,α-Difluoro-β-amino Acids.
✍ Natalie A. Fokina; Andrei M. Kornilov; Valery P. Kukhar 📂 Article 📅 2010 🏛 John Wiley and Sons ⚖ 31 KB 👁 1 views

## Abstract ChemInform is a weekly Abstracting Service, delivering concise information at a glance that was extracted from about 100 leading journals. To access a ChemInform Abstract of an article which was published elsewhere, please select a “Full Text” option. The original article is trackable v

Ion-molecule reactions of 2-methoxyethan
Ion-molecule reactions of 2-methoxyethanol with some amines, carboxylic acids and amino acids under chemical ionization conditions
✍ Jaana M. H. Pakarinen; Harri Moisio; Sanna Holopainen; Pirjo Vainiotalo 📂 Article 📅 1999 🏛 John Wiley and Sons 🌐 English ⚖ 68 KB 👁 2 views

2-Methoxyethanol chemical ionization of amines, carboxylic acids and amino acids has been found to produce numerous adduct ions. The most intense adduct ions for amines are [M H] and [M 77] , for carboxylic acids [M 27] , [M 59] and [M 77] , and for amino acids [M H] , [M 13] , [M 27] and [M 77] . E