THE FORMATION AND INTRAMOLECULAR ACYLATION OF A 1,2-DIHYDRO-β-CARBOLINE DERIVATIVE; A MODEL SEQUENCE FOR THE TOTAL SYNTHESIS OF FUMITREMORGINS.

DOI: 10.1016/S0040-4039(00)85522-7

Source and publish data:

Tetrahedron Letters p. 521 - 524 (1986)

Update date:2022-08-02

Topics:

Authors:

Harrison, David M.

Sharma, Ram Bilas

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Article abstract of DOI:10.1016/S0040-4039(00)85522-7

The racemic 2-tosyltetrahydro-β-carbolines 4c and 4d each gave the β-carboline 5 on treatment with sodium methoxide; under similar conditions 7c furnished the pentacycle 2c.

Full text of DOI:10.1016/S0040-4039(00)85522-7

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