Journal of Organic Chemistry p. 5578 - 5583 (1991)
Update date:2022-09-26
Topics:
Cook, Gregory R.
Stille, John R.
The <3,3> charge-accelerated rearrangement of N-allyl-N-isobutyl enamine substrates to γ,δ-unsaturated imine products and subsequent reduction to the corresponding N-alkyl δ,ε-unsaturated amines is reported.Several routes to the N-allyl-N-isobutyl enamine
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Doi:10.1080/00397919108019763
(1991)Doi:10.1002/ejoc.201101091
(2011)Doi:10.1016/j.bmcl.2016.11.042
(2017)Doi:10.1055/s-0030-1258227
(2010)Doi:10.1016/j.tetlet.2010.11.003
(2011)Doi:10.1016/j.tetlet.2010.11.025
(2011)
