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Chemistry of acetylenic ethers. LIX: Alk-1-enyl alk-1-ynyl ethers, thioethers and selenoethers

✍ Scribed by L. Brandsma; J. F. Arens

Publisher
Elsevier Science
Year
2010
Tongue
English
Weight
480 KB
Volume
81
Category
Article
ISSN
0165-0513

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✦ Synopsis

Abstract

The compounds listed in tables I and II have been prepared by the reaction schemes A, B and C.

Acid hydrolysis of vinyloxyethyne produces vinyl acetate. Rearrangement of 3‐hydroxy‐3‐methyl‐1‐vinyloxy‐1‐butyne XIV by acid gives the vinyl ester of 2,2‐dimethylacrylic acid XV.

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