Journal of Organic Chemistry p. 3730 - 3732 (1986)
Update date:2022-08-15
Topics:
Oku, Akira
Yamaura, Yasunari
Harada, Toshiro
A hydride abstraction-recombination mechanism in the insertion of the α-C-H bond of alkoxides by norcaranylidene carbenoid is proposed on the basis of the preferential endo stereoselectivity at the carbenic carbon of the insertion products
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Doi:10.1039/jr9600000314
(1960)Doi:10.1016/j.bmcl.2007.11.059
(2008)Doi:10.1021/jo00358a002
(1986)Doi:10.1039/b715973k
(2002)Doi:10.1016/j.ejmech.2007.02.004
(2008)Doi:10.1021/jm7011547
(2008)
