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The paternò-büchi reaction as a route to medium-ring ethers and acetals

✍ Scribed by Howard A.J. Carless; John Beanland; Samson Mwesigye-Kibende


Book ID
104233497
Publisher
Elsevier Science
Year
1987
Tongue
French
Weight
202 KB
Volume
28
Category
Article
ISSN
0040-4039

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✦ Synopsis


Photochemical reactions of the vinyloxyketones

(3) give a regioselective intramolecular cycloaddition to afford oxetanes (4); the latter react stereospecifically with methanol to yield medium-ring acetals (51.


📜 SIMILAR VOLUMES


The Paternò-Büchi Reaction of 3-Heteroat
✍ Bach, Thorsten 📂 Article 📅 1997 🏛 John Wiley and Sons 🌐 English ⚖ 764 KB

## Abstract The preparation of 3‐heteroatom‐substituted oxetanes by the Paternò‐Büchi reaction, and their application in synthesis are reviewed. 3‐Oxetanols and 3‐aminooxetanes are the two most important oxetanes in this respect. By tuning the electronic properties of the enol and enamine substrate