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Reductive elimination and skeletal rearrangement of β-hydroxy selenide derivatives of bicyclo[4.2.l]nonatriene in a super acid medium

✍ Scribed by Huub M. J. Gillissen; Pieter Schipper; Henk M. Buck


Book ID
104588270
Publisher
Elsevier Science
Year
2010
Tongue
English
Weight
230 KB
Volume
99
Category
Article
ISSN
0165-0513

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✦ Synopsis


Abstract

In sulfur dioxide the β‐hydroxy selenides 1 and 2 produce rearranged selenides 6 and 7 upon addition of fluorosulfonic acid. Reductive elimination and subsequent attack of the selenenyl electrophile on the etheno bridge cause migration of the butadiene moiety.