Journal of Organic Chemistry p. 4943 - 4953 (1987)
Update date:2022-08-02
Topics:
Clive, Derrick L.J.
Boivin, Taryn L.B.
Angoh, A. Gaeetan
Enamines react with Michael acceptors 8-10 to produce ketones that, on treatment with lithium acetylides, afford hydroxy acetylenes 3.These compounds then undergo radical cyclization when treated with triphenyltin hydride and AIBN.The products 6 are forme
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Doi:10.1016/S0040-4020(01)88112-6
(1986)Doi:10.1055/s-0028-1083498
(2008)Doi:10.1055/s-0028-1083549
(2008)Doi:10.1039/P29870000193
(1987)Doi:10.1016/j.tetasy.2008.10.006
(2008)Doi:10.1246/bcsj.60.201
(1987)
