Tetrahedron Letters p. 3727 - 3730 (1990)
Update date:2022-08-03
Topics:
Enholm
Burroff
Jaramillo
A benzyl oxime ether tethered to a terminal alkyne efficiently undergoes a free radical hydrostannylation reaction to afford five- and six-membered rings bearing a protected amine and a vinyl stannane functionally. These products were subsequently protiodestannylated to obtain the unsubstituted exo-methylene compounds.
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Doi:10.1016/S0040-4039(00)89045-0
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(1993)Doi:10.1021/ic50018a002
(1964)Doi:10.1021/ja01529a060
(1959)Doi:10.1055/s-0030-1258453
(2011)Doi:10.1021/acs.orglett.5b00103
(2015)
