A tandem Horner−Emmons olefination−conjugate addition approach to the synthesis of 1,5-disubstituted-6-azabicyclo[3.2.1]octanes based on the AE ring structure of the norditerpenoid alkaloid methyllycaconitine

David J. Callis; Noel F. Thomas; David P. J. Pearson; Barry V. L. Potter

doi:10.1021/jo9519672

A tandem Horner−Emmons olefination−conjugate addition approach to the synthesis of 1,5-disubstituted-6-azabicyclo[3.2.1]octanes based on the AE ring structure of the norditerpenoid alkaloid methyllycaconitine

David J. Callis, Noel F. Thomas, David P. J. Pearson, Barry V. L. Potter

Department of Pharmacy & Pharmacology

Research output: Contribution to journal › Article › peer-review

25 Citations (Scopus)

Original language	English
Pages (from-to)	4634-4640
Journal	Journal of Organic Chemistry
Volume	61
Issue number	14
DOIs	https://doi.org/10.1021/jo9519672
Publication status	Published - 1 Jan 1996

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10.1021/jo9519672

http://dx.doi.org/10.1021/jo9519672

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Callis, D. J., Thomas, N. F., Pearson, D. P. J., & Potter, B. V. L. (1996). A tandem Horner−Emmons olefination−conjugate addition approach to the synthesis of 1,5-disubstituted-6-azabicyclo[3.2.1]octanes based on the AE ring structure of the norditerpenoid alkaloid methyllycaconitine. Journal of Organic Chemistry, 61(14), 4634-4640. https://doi.org/10.1021/jo9519672

A tandem Horner−Emmons olefination−conjugate addition approach to the synthesis of 1,5-disubstituted-6-azabicyclo[3.2.1]octanes based on the AE ring structure of the norditerpenoid alkaloid methyllycaconitine. / Callis, David J.; Thomas, Noel F.; Pearson, David P. J.; Potter, Barry V. L.

In: Journal of Organic Chemistry, Vol. 61, No. 14, 01.01.1996, p. 4634-4640.

Research output: Contribution to journal › Article › peer-review

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