Abstract
The cycloaddition of ynamines uith cyclohexenones occurs in the presence of magnesium bromide at the carbonyl but proceeds by attack on the carbon-carbon double bond without catalyst whereas, in contrast, with cyclopentenones, the reaction takes place at the carbon-carbon double bond with or without magnesium bromide.
Original language | English |
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Pages (from-to) | 725-728 |
Number of pages | 4 |
Journal | Tetrahedron Letters |
Volume | 22 |
Issue number | 8 |
Publication status | Published - 1 Jan 1981 |