Tetrahedron Letters p. 1469 - 1472 (1986)
Update date:2022-07-29
Topics:
Epling, Gary A.
Florio, Emily
The "Photo-Birch" reduction of o-, m-, and p-xylene, using NaBH4, 1,3-dicyanobenzene, and photolysis, gives 1,4-dienes as products.The regioselectivity of these reactions is greatly different from the normal Birch reduction.
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Doi:10.1002/chem.200390099
(2003)Doi:10.1016/S0040-4039(03)00242-9
(2003)Doi:10.1039/c4ce00103f
(2014)Doi:10.1246/cl.1975.87
(1975)Doi:10.1039/c6ob01273f
(2016)Doi:10.1016/S0040-4020(01)97526-X
(1974)
