𝔖 Bobbio Scriptorium
✦   LIBER   ✦

The mechanism of hydroxylamine addition to α,β-unsaturated esters

✍ Scribed by Helmet Stamm; Harald Steudle

Publisher
Elsevier Science
Year
1976
Tongue
French
Weight
217 KB
Volume
17
Category
Article
ISSN
0040-4039

No coin nor oath required. For personal study only.

📜 SIMILAR VOLUMES

The mechanism of hydroxylamine addition
The mechanism of hydroxylamine addition to α, β-unsaturated esters
✍ K.R. Fountain; Robert Erwin; Terry Early; Horst Kehl 📂 Article 📅 1975 🏛 Elsevier Science 🌐 French ⚖ 232 KB

The addition of&-nucleophiles to unsaturated substrates has recently drawn both theoretical1 and experimental attention. 2 In this report we present data pertaining to the addition ofd-nucleophiles to Cr,$ -unsaturated esters, in particular ethyl cinnamate. We 'lWe h ave also obtained oils having h

A stereoselective michael addition of α-
A stereoselective michael addition of α-lithiated phosphonates to α,β-unsaturated esters
✍ Masahiko Yamaguchi; Yukiharu Tsukamoto; Akio Hayashi; Toru Minami 📂 Article 📅 1990 🏛 Elsevier Science 🌐 French ⚖ 123 KB

a-Lithiated phosphonates added to a&unsaturated t-butyl esters in 1,Gmanner giving anti-3,4-disubstituted-4-phosphorylbutanoates in high yields. /~~%~ylam%omethyl)phosphonates were prepared from dialkyl phosphite, dibenzylamine, and formaldehyde: See; R. Tyka, Tetrahedron Lett., 1970, 677.

Stereoselective conjugate additions of b
Stereoselective conjugate additions of benzyl sulphoxides to α,β-unsaturated esters
✍ Mike Casey; Ajith C. Manage; Ray S. Gairns 📂 Article 📅 1989 🏛 Elsevier Science 🌐 French ⚖ 281 KB

We recently reported the first examples of conjugate additions of alkyl sulphoxides to unsaturated esters,\* These reactions proceed with good selectivity and provide a promising new method for carrying out