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The synthesis and stereochemistry of odorine

Journal Article


Abstract


  • The stereochemistry of naturally occurring odorine has been established as (+)-(E, 2S, 2′R)-2-methyl- N-[l′-(l″-oxo-3″-phenylprop-2″-enyl)pyrrolidin-2′-yl]butanamide by synthesis of (-)-odorine and (+)-dihydroodorine from L-proline. © 1980, CSIRO. All rights reserved.

Publication Date


  • 1980

Citation


  • Babidge, P. J., Massy-Westropp, R. A., Pyne, S. G., Shiengthong, D., Ungphakon, A., & Veerachat, G. (1980). The synthesis and stereochemistry of odorine. Australian Journal of Chemistry, 33(8), 1841-1815. doi:10.1071/CH9801841

Scopus Eid


  • 2-s2.0-84970557873

Web Of Science Accession Number


Start Page


  • 1841

End Page


  • 1815

Volume


  • 33

Issue


  • 8

Abstract


  • The stereochemistry of naturally occurring odorine has been established as (+)-(E, 2S, 2′R)-2-methyl- N-[l′-(l″-oxo-3″-phenylprop-2″-enyl)pyrrolidin-2′-yl]butanamide by synthesis of (-)-odorine and (+)-dihydroodorine from L-proline. © 1980, CSIRO. All rights reserved.

Publication Date


  • 1980

Citation


  • Babidge, P. J., Massy-Westropp, R. A., Pyne, S. G., Shiengthong, D., Ungphakon, A., & Veerachat, G. (1980). The synthesis and stereochemistry of odorine. Australian Journal of Chemistry, 33(8), 1841-1815. doi:10.1071/CH9801841

Scopus Eid


  • 2-s2.0-84970557873

Web Of Science Accession Number


Start Page


  • 1841

End Page


  • 1815

Volume


  • 33

Issue


  • 8