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Boron-mediated stereoselective syntheses of ?,?-disubstituted allenamides

Journal Article


Abstract

  • Propargylic boranes generated by lithiation of optically active N-propargyloxazolidinones undergo reaction with a range of aldehydes to produce γ,γ-disubstituted allenamides with good diastereoselectivity. © 2005 American Chemical Society.

Publication Date

  • 2005

Citation

  • Hyland, C. J. T., & Hegedus, L. S. (2005). Boron-mediated stereoselective syntheses of ?,?-disubstituted allenamides. Journal of Organic Chemistry, 70(21), 8628-8630. doi:10.1021/jo051385c

Scopus Eid

  • 2-s2.0-26844453978

Start Page

  • 8628

End Page

  • 8630

Volume

  • 70

Issue

  • 21

Abstract

  • Propargylic boranes generated by lithiation of optically active N-propargyloxazolidinones undergo reaction with a range of aldehydes to produce γ,γ-disubstituted allenamides with good diastereoselectivity. © 2005 American Chemical Society.

Publication Date

  • 2005

Citation

  • Hyland, C. J. T., & Hegedus, L. S. (2005). Boron-mediated stereoselective syntheses of ?,?-disubstituted allenamides. Journal of Organic Chemistry, 70(21), 8628-8630. doi:10.1021/jo051385c

Scopus Eid

  • 2-s2.0-26844453978

Start Page

  • 8628

End Page

  • 8630

Volume

  • 70

Issue

  • 21