Tetrahedron p. 6345 - 6356 (1988)
Update date:2022-07-30
Topics:
Vincens, M.
Fadel, R.
Vidal, M.
Cyclopropene-2 ylalkyl radical, obtained by tributyltin hydride reduction of 2,3-dialkylcyclopropene-2 ylmethylketones follows a very selective evolution according to the substituents in the ring.Ring enlarged products (2,3,5-trialkylfuranes) and olefinic or saturated products resulting from ring cleavage can be isolated.
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Doi:10.1016/0021-9517(86)90268-X
(1986)Doi:10.1016/S0040-4039(00)80814-X
(1988)Doi:10.1016/j.tet.2009.12.017
(2010)Doi:10.1021/om00110a012
(1989)Doi:10.1016/j.bmc.2016.04.025
(2016)Doi:10.1016/0031-9422(90)80035-F
(1990)
