Title of article
The cycloaddition of cyclopropenes to enones
Author/Authors
Al Dulayymi، نويسنده , , Juma’a R and Baird، نويسنده , , Mark H. and Hussain، نويسنده , , Helmi H and Alhourani، نويسنده , , Baker J and Alhabashna، نويسنده , , Al-Meqdad Y and Coles، نويسنده , , Simon J and Hursthouse، نويسنده , , Michael B، نويسنده ,
Issue Information
هفته نامه با شماره پیاپی سال 2000
Pages
4
From page
4205
To page
4208
Abstract
A number of 1- and 1,2-disubstituted cyclopropenes undergo [4+2]-cycloaddition to methyl vinyl ketone or acrolein at ambient temperature to produce 2-oxabicyclo[4.1.0]hept-3-enes. When 1-phenyl-2-trimethylsilyl-cyclopropene is treated with 0.4 mol. equiv. of m-chloroperbenzoic acid, the derived ring-opened enone undergoes [4+2]-cycloaddition to the remaining starting material at ambient temperature.
Journal title
Tetrahedron Letters
Serial Year
2000
Journal title
Tetrahedron Letters
Record number
1637810
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