Issue 13, 1997

Bicyclo[3.3.1]nonanes as synthetic intermediates. Part 21.1 Enantiodivergent synthesis of the cis,cis 2,6-disubstituted piperidin-3-ol chiral building block for alkaloid synthesis

Abstract

Enantiodivergent synthesis of the enantio-pure cis,cis 3-protected 2,6-disubstituted piperidin-3-ol 1 has been achieved via a biochemical method, and the absolute stereochemistry of (+)-1 has been established by its conversion into the known piperidine (-)-17. The utility of 1 as a chiral building block for alkaloid synthesis is demonstrated by the total synthesis of (-)-cassine and (+)-spectaline.

Article information

Article type
Paper

J. Chem. Soc., Perkin Trans. 1, 1997, 2005-2014

Bicyclo[3.3.1]nonanes as synthetic intermediates. Part 21.1 Enantiodivergent synthesis of the cis,cis 2,6-disubstituted piperidin-3-ol chiral building block for alkaloid synthesis

T. Momose, N. Toyooka and M. Jin, J. Chem. Soc., Perkin Trans. 1, 1997, 2005 DOI: 10.1039/A608490G

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