Studies of the tetrathiafulvalene mediated radical-polar crossover reaction directed toward the total synthesis of alkaloid natural products

DOI: 10.1016/0040-4039(96)00306-1

Source and publish data:

Tetrahedron Letters p. 2511 - 2514 (1996)

Update date:2022-08-03

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Authors:

Kizil, Murat

Lampard, Christopher

Murphy, John A.

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Article abstract of DOI:10.1016/0040-4039(96)00306-1

The carbon skeleton of octahydro-1H-pyrrolo[2,3-d]carbazole (4), a tetracylic sub-unit which is common to a wide range of alkaloid natural products has been prepared by two approaches which exploit the one-pot radical-polar crossover chemistry mediated by

Full text of DOI:10.1016/0040-4039(96)00306-1

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