Title of article
Halogen effect on tandem [4+2] cycloaddition/aromatization sequence of allenyl 2-halo-3-vinylcyclohex-2-enyl ether
Author/Authors
Hatae، نويسنده , , Noriyuki and Suzuki، نويسنده , , Ichiro and Choshi، نويسنده , , Tominari and Hibino، نويسنده , , Satoshi and Okada، نويسنده , , Chiaki and Toyota، نويسنده , , Eiko، نويسنده ,
Issue Information
هفته نامه با شماره پیاپی سال 2014
Pages
3
From page
4146
To page
4148
Abstract
Steric and enthalpic effects of substituents on diene moieties play a crucial role in intramolecular cycloaddition reactions. Allenyl 2-halogenated-3-vinylcyclohex-2-enyl ethers underwent a tandem [4+2] cycloaddition/aromatization reaction to afford the corresponding tetrahydro-3H-naphtho[1,8-bc]furan compound in high yield.
Keywords
8-bc]furan , Switching reaction pathway , Allene , Halogenated diene
Journal title
Tetrahedron Letters
Serial Year
2014
Journal title
Tetrahedron Letters
Record number
1890163
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