𝔖 Bobbio Scriptorium
✦   LIBER   ✦

Nucleophilic substitution and electron transfer in the ring-opening reactions of β-lactones: A short review

✍ Scribed by Zbigniew Jedlinński


Publisher
Journal of Heterocyclic Chemistry
Year
2001
Tongue
English
Weight
117 KB
Volume
38
Category
Article
ISSN
0022-152X

No coin nor oath required. For personal study only.

✦ Synopsis


Abstract

Nucoleaophilic substitution by activated organic anions and single and two electron transfer in ring opening reactions of 4‐membered β‐lactones are described.


📜 SIMILAR VOLUMES


ChemInform Abstract: Carbon Transfer Rea
✍ K. SINGH; J. SINGH; H. SINGH 📂 Article 📅 2010 🏛 John Wiley and Sons ⚖ 40 KB 👁 2 views

Carbon Transfer Reactions of Functionalized Oxazolidines and Their Open Chain Enamine Tautomers to Enamine Nucleophiles. A Facile Synthesis of Substituted Pyridines and Ring Annulated Derivatives. -Oxazolidines like (II) capable of existing as enamine tautomers and having additional electrophilic a

The influence of some steric and electro
✍ Thomas A. Emokpae; Nkechi V. Atasie 📂 Article 📅 2005 🏛 John Wiley and Sons 🌐 English ⚖ 90 KB 👁 1 views

## Abstract Kinetic studies are reported for the reactions with aniline in benzene of a series of X‐phenyl 2,4,6‐trinitrophenyl ethers [X = H; 2‐, 3‐, 4‐CH~3~; 2,4‐, or 2,6‐(CH~3~)~2~] a–f, and the results compared with those of the corresponding nitro derivatives. In the methyl series, kinetic dat