Acyclic diastereoselection as a synthetic route to quassinoids: a Claisen rearrangement based strategy for bruceantin
- 1 May 1985
- journal article
- research article
- Published by American Chemical Society (ACS) in Journal of the American Chemical Society
- Vol. 107 (9), 2730-2737
- https://doi.org/10.1021/ja00295a027
Abstract
No abstract availableThis publication has 8 references indexed in Scilit:
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- An approach to the BCDE ring of quasimarinThe Journal of Organic Chemistry, 1982
- Conversion of Quassin into 15β-[(E)-3,4-dimethyl-2-pentenoyloxy]quassin. A D-Ring Analog of BruceantinBulletin of the Chemical Society of Japan, 1981
- Steroide und Sexualhormone. 261. Mitteilung. Quassinoide Bitterstoffe II. Partialsynthetischer Zugang zu Quassin: Überführung von Testosteron in eine Schlüsselverbindung mit angulärer 8β‐MethylgruppeHelvetica Chimica Acta, 1980
- Synthesis of a model for the BCE ring system of bruceantin. A caveat on the cyclohexene .fwdarw. trans diaxial diol conversionThe Journal of Organic Chemistry, 1980