Experiments Directed toward a Total Synthesis of Dynemicin A: A Solution to the Stereochemical Problem

DOI: 10.1021/jo00093a002

Source and publish data:

Journal of Organic Chemistry p. 3752 - 3754 (1994)

Update date:2022-08-05

Topics:

Authors:

Yoon, Taeyoung

Shair, Matthew D.

Danishefsky, Samuel J.

Shulte, Gayle K.

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Article abstract of DOI:10.1021/jo00093a002

The stereochemical issues required for a total synthesis of dynemicin A (1) have been resolved by employing an intramolecular Diels-Alder reaction and a diastereoselective addition of a magnesioacetylide to a quinoline under the influence of methyl chloro

Full text of DOI:10.1021/jo00093a002

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