Tetrahedron Letters p. 4653 - 4656 (1992)
Update date:2022-08-10
Topics:
Barlow, Michael G.
Sibous, Lakhdar
Tipping, Anthony E.
The initial dihydropyridines from Diels-Alder addition of dienes to trichloro-1,2,4-triazine, and loss of N2, undergo intramolecular addition with hexa-1,5-diene and cyclo-octa-1,5-diene, also [1,5]H sigmatropic shift with diallyl ether, and [1,5]H shift and partial aromatisation with cyclododeca-1,5,9-triene.
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