Title of article
The reaction of selenoaldehydes with 2-methoxyfuran using their generation by retro Diels–Alder reaction
Author/Authors
Zhou، نويسنده , , Aojia and Segi، نويسنده , , Masahito and Nakajima، نويسنده , , Tadashi، نويسنده ,
Issue Information
هفته نامه با شماره پیاپی سال 2003
Pages
4
From page
1179
To page
1182
Abstract
Selenoaldehydes, regenerated by thermal retro Diels–Alder reaction of anthracene cycloadducts under neutral conditions, reacted with 2-methoxyfuran to give methyl penta-2,4-dienoates along with the deposition of elemental selenium. In a similar reaction with 2-methoxyfuran using thioaldehyde, thiirane compound was isolated. This suggests the formation of selenirane intermediates in the above reaction.
Keywords
Diels–Alder reactions , dienoates , selenium and compounds , seleniranes
Journal title
Tetrahedron Letters
Serial Year
2003
Journal title
Tetrahedron Letters
Record number
1660506
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