Studies directed toward the total synthesis of tetronolide 1. An enantioselective synthesis of the octahydronaphthalene unit

DOI: 10.1016/S0040-4039(00)79871-6

Source and publish data:

Tetrahedron Letters p. 4091 - 4094 (1991)

Update date:2022-08-04

Topics:

Authors:

Boeckman Jr., Robert K.

Barta, Thomas E.

Nelson, Scott G.

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Article abstract of DOI:10.1016/S0040-4039(00)79871-6

An efficient enantioselective route to the octahydronaphthalene unit present in tetronolide (1), the stereochemically complex aglycone common to the tetrocarcins, a novel group of antitumor substances, is described. The sequence employs the intramolecular

Full text of DOI:10.1016/S0040-4039(00)79871-6

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