Synthesis p. 411 - 416 (1994)
Update date:2022-08-03
Topics:
Bourlot
Desarbre
Merour
The Baeyer-Villiger rearrangement of substituted 1H-indole-3-carbaldehydes afforded the corresponding substituted 1,2-dihydro-3H-indol-3-ones. The influence of 3-carbonyl and 1-protecting groups has been examined. Reaction has been extended to 1H-indole-2-carbaldehydes and used for synthesis of 1-(phenylsulfonyl)-1H-indol-2-yl trifluoromethanesulfonate.
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Doi:10.1007/BF00697152
()Doi:10.1002/chem.202100390
(2021)Doi:10.1016/S0040-4020(01)85070-5
(1994)Doi:10.1021/ol5003219
(2014)Doi:10.1055/s-0040-1707909
(2020)Doi:10.1002/pola.26987
(2014)
