Tetrahedron Letters p. 2437 - 2440 (1983)
Update date:2022-07-31
Topics: Synthesis Regioselectivity Column chromatography Yield Catalyst Solvent Optimization Reagent Stirring Anilines TLC (thin-layer chromatography) NMR (nuclear magnetic resonance) Purification Workup Reaction Time Functional group Byproduct 3-substituted indoles
Wierenga, Wendell
Griffin, John
Warpehoski, Martha A.
Borane-mediated reductive elimination of α-thiomethyl-, α-hydroxy-, or α-alkoxy-, α'-substituted oxindoles affords 3-substituted indoles in high yield.Isatins, available via several routes from oxindoles, also afford indoles.
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(1982)Doi:10.1021/jo00150a018
(1983)Doi:10.1021/ol0266471
(2002)Doi:10.1016/0022-328X(82)80003-X
(1982)Doi:10.1021/jo00152a003
(1983)Doi:10.1016/S0960-894X(02)00085-9
(2002)
