Chemistry of acetylenic ethers XLVI: Addition of thiols to acetylenic ethers

HJ Alkema, JF Arens

Index: Alkema,H.J.; Arens,J.F. Recueil des Travaux Chimiques des Pays-Bas, 1960 , vol. 79, p. 1257 - 1281

Full Text: HTML

Citation Number: 27

Abstract

Many addition-reactions of acetylenic ethers have been studied 1 in the past. In accordance with the expected polarisation of ethoxy- ethyne (I) 2 it was found that nucleophilic reagents always become attached to the acarbon atom, whereas electrophilic reagents interact with the p-carbon atom. The acid-catalysed additions of water, alcohols, etc. also fit into this picture because the catalysing electro- philic hydrogen ion becomes bound to the p-carbon atom.

Related Articles:

Electrotelluration: A new approach to tri-and tetrasubstituted alkenes

[Marino, Joseph P.; Nguyen, Hanh Nho Journal of Organic Chemistry, 2002 , vol. 67, # 18 p. 6291 - 6296]

Electrotelluration: A new approach to tri-and tetrasubstituted alkenes

[Marino, Joseph P.; Nguyen, Hanh Nho Journal of Organic Chemistry, 2002 , vol. 67, # 18 p. 6291 - 6296]

Dithio??und Thionester, 50. α, β??Acetylenische Thioamide, Dithioester und Thionester

[Hartke, Klaus; Gerber, Hans-Dieter; Roesrath, Ulrich Liebigs Annalen der Chemie, 1991 , # 9 p. 903 - 916]

More Articles...