Title of article :
Stereoselective intramolecular Diels–Alder reactions of 3-alkenyl(oxy)-2(1H)-pyrazinones
Author/Authors :
De Borggraeve، نويسنده , , Wim M. and Rombouts، نويسنده , , Frederik J.R. and Verbist، نويسنده , , Bie M.P. and Van der Eycken، نويسنده , , Erik V. and Hoornaert، نويسنده , , Georges J.، نويسنده ,
Issue Information :
هفته نامه با شماره پیاپی سال 2002
Pages :
3
From page :
447
To page :
449
Abstract :
Dichloropyrazinones are reacted with alkenolates or a Grignard reagent in order to tether a dienophilic side-chain at the 3-position. The compounds smoothly undergo intramolecular Diels–Alder reaction forming tricyclic ring systems. The reactions proceed completely stereoselective yielding only endo adducts. In the case of the alkenylpyrazinone, the core skeleton of the breviamides is obtained.
Keywords :
cycloaddition , Pyrazinone , Diels–Alder reaction , brevianamide
Journal title :
Tetrahedron Letters
Serial Year :
2002
Journal title :
Tetrahedron Letters
Record number :
1649301
Link To Document :
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