𝔖 Bobbio Scriptorium
✦   LIBER   ✦

Synthesis, stereochemistry, intramolecular cyclization, and rates of hydrolysis of adenosine 2′,3′-acetals

✍ Scribed by Venkatesalu Bakthavachalam; Lee-Gin Lin; Xavier M. Cherian; Anthony W. Czarnik

Book ID
107725688
Publisher
Elsevier Science
Year
1987
Tongue
English
Weight
919 KB
Volume
170
Category
Article
ISSN
0008-6215

No coin nor oath required. For personal study only.

📜 SIMILAR VOLUMES

Cyclopentane synthesis and annulation: I
Cyclopentane synthesis and annulation: Intramolecular radical cyclization of acetals
✍ Veejendra K. Yadav; Alex G. Fallis 📂 Article 📅 1988 🏛 Elsevier Science 🌐 French ⚖ 232 KB

A general procedure for cyclopentane synthesis based on free-radical cyclization of thioacetals is described. This permits the rapid assembly, by intramolecular annulation, of various ring systems bearing useful functionality for use in total synthesis.

Intramolecular cyclization of ω-haloalky
Intramolecular cyclization of ω-haloalkylsubstituted thiophosphorylacetonitriles: Synthesis and stereochemistry of 3-cyano-2-oxo-1,2-thiaphosphacyclanes
✍ Irene L. Odinets; Natalya M. Vinogradova; Konstantin A. Lyssenko; Michail Yu. An 📂 Article 📅 2002 🏛 John Wiley and Sons 🌐 English ⚖ 295 KB

## Abstract Intramolecular S‐alkylation in a series of ω‐haloalkyl‐substituted thiophosphorylacetonitriles **__5–7__** presents an effective synthetic route to the hitherto unknown 3‐cyano‐2‐oxo‐1,2‐thiaphospholanes **__14__** and thiaphosphinanes **__15__**. The compounds were obtained as a mixtur