Addition of (pseudo) halogens across the triple bond of 1,4-dichlorobut-2-yne, followed by a 1,4-elimination, provides a very simple preparation of ten novel butadienes. In recent years there has been a great deal of interest in asymmetrically substituted butadienes, both for theoretical reasons an
β¦ LIBER β¦
A new preparation of 3-substituted 2-(p-toluenesulfonyl)-1,3-dienes
β Scribed by Thomas G. Back; Enoch K.Y. Lai; K.Raman Muralidharan
- Book ID
- 104240322
- Publisher
- Elsevier Science
- Year
- 1989
- Tongue
- French
- Weight
- 135 KB
- Volume
- 30
- Category
- Article
- ISSN
- 0040-4039
No coin nor oath required. For personal study only.
β¦ Synopsis
The title compounds were prepared by addition-elimination reactions of 2-(p-toluenesulfonyl)-2,3-butadien-l-01.
The latter was readily obtained from 1,4-dichloro-2-butyne by selenosulfonation, reductive elimination of chlorine and [2,3] sigmatropic rearrangement of the corresponding selenoxide.
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