A model study directed towards a practical enantioselective total synthesis of (-)-morphine

DOI: 10.1055/s-1992-34161

Source and publish data:

Synthesis p. 174 - 178 (1992)

Update date:2022-08-11

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Authors:

Hudlicky

Boros Boros

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Article abstract of DOI:10.1055/s-1992-34161

A tricyclic ring system 10 containing the stereogenic centers of the nonaromatic portion of morphine (1) has been prepared in eight steps from toluene by the combination of microbial oxidation and intramolecular Diels-Alder cycloaddition followed by a Cop

Full text of DOI:10.1055/s-1992-34161

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