Tetrahedron Letters p. 4949 - 4952 (1982)
Update date:2022-08-03
Topics:
Barton, Derek H.R.
Lusinchi, Xavier
Milliet, Pierre
Phenylseleninic anhydride reacts rapidly with indolines at 0 deg C to give, when the β-position is substituted, the corresponding indoles.When the β-position is unsubstituted β-phenylselenoindoles are formed.These are readily reduced by nickel boride to the parent indole.Tetrahydroisoquinoline is dehydrogenated with comparable ease.Phenylseleninic acid is also an efficient agent for these dehydrogenations.
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(1986)Doi:10.1071/CH9851685
(1985)Doi:10.1039/b803043j
(2008)Doi:10.1016/j.tetlet.2008.05.043
(2008)Doi:10.1016/j.tet.2008.05.050
(2008)Doi:10.1016/S0040-4039(00)98247-9
(1985)
