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The regioselectivity of [6+4] cycloadditions of dienamines to fulvenes.

✍ Scribed by Lee C. Dunn; K.N. Houk

Book ID
104212228
Publisher
Elsevier Science
Year
1978
Tongue
French
Weight
209 KB
Volume
19
Category
Article
ISSN
0040-4039

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## 1. Introduction. the synthetic application of dienamines I [I] as Diels-Alder dienes is well documented'). The main features of their reactions with dienophiles are high reactivity and the fact that the R,N group controls the regiochemistry of the cycloaddition. For example, the use of electron-