Facile Hetero??Diels??Alder Reaction of α, β??Unsaturated Acyl Cyanides and Enol Ethers: Syntheses of 2??Alkoxy??3, 4??dihydro??2H??Pyran??6??carbonitriles
RA John, V Schmid, H Wyler
Index: John, Robert A.; Schmid, Vincent; Wyler, Hugo Helvetica Chimica Acta, 1987 , vol. 70, p. 600 - 606
Full Text: HTML
Citation Number: 20
Abstract
1. Introduction. - The reaction of a,/3 -unsaturated carbonyl compounds with alkyl vinyl ethers, a classical example of a Die1.r-Alder cycloaddition of inverse electron demand [I], makes available various derivatives of 2-alkoxy-3,4-dihydro-2H-pyrans useful in the synthesis of carbohydrates [2], thromboxanes [3], and spiroacetals [4]. When elevated temperature is used for this reaction, the theoretically favoured 'endo ' adducts are not the exclusive products. ...
Related Articles:
Synthesis and characterization of naphth-annelated thiophene analogs
[Clement, J. Arul; Mohanakrishnan, Arasambattu K. Tetrahedron, 2010 , vol. 66, # 13 p. 2340 - 2350]
Synthesis and anti-cancer activity of C-ring-functionalized prodigiosin analogues
[Journal of Medicinal Chemistry, , vol. 50, # 7 p. 1528 - 1536]