STEREOCONTROLLED FORMATION OF 1,2-DIHYDROINDOLES

DOI: 10.1016/S0040-4020(01)90054-7

Source and publish data:

Tetrahedron p. 1147 - 1156 (1987)

Update date:2022-09-26

Topics:

Authors:

Veenstra, S.J.

Fortgens, H.P.

Vijn, R.J.

Jong, B.S. de

Speckamp, W.N.

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Article abstract of DOI:10.1016/S0040-4020(01)90054-7

Imines 4 cyclize stereoselectively to dihydroindoles 2 upon use of a Li or Na alkoxide-alcohol combination.Depending on the type of alcohol applied either cis (2C) or trans (2T) spiroindolines 2 are formed.In case of imines 4 derived from electron-rich ar

Full text of DOI:10.1016/S0040-4020(01)90054-7

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