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Synthesis of (+)-(S)-(E)-¿-Hydroxy-¿,ß-enoates from a Camphor-derived ¿-Sulfinyl Acetate Ester

Journal Article


Abstract


  • The synthesis of (+)-(S)-(E)-γ-hydroxy-α,β-enoates 4 in moderate enantiomeric purities (36-54%) from the reaction of the camphor-derived α-sulfinyl acetate ester 3 with aldehydes is described.

Publication Date


  • 1996

Citation


  • Dixon, C. E., Hellmund, K., & Pyne, S. G. (1996). Synthesis of (+)-(S)-(E)-¿-Hydroxy-¿,ß-enoates from a Camphor-derived ¿-Sulfinyl Acetate Ester. Journal of Chemical Research - Part S, (8), 372-373.

Scopus Eid


  • 2-s2.0-2742514642

Web Of Science Accession Number


Start Page


  • 372

End Page


  • 373

Issue


  • 8

Abstract


  • The synthesis of (+)-(S)-(E)-γ-hydroxy-α,β-enoates 4 in moderate enantiomeric purities (36-54%) from the reaction of the camphor-derived α-sulfinyl acetate ester 3 with aldehydes is described.

Publication Date


  • 1996

Citation


  • Dixon, C. E., Hellmund, K., & Pyne, S. G. (1996). Synthesis of (+)-(S)-(E)-¿-Hydroxy-¿,ß-enoates from a Camphor-derived ¿-Sulfinyl Acetate Ester. Journal of Chemical Research - Part S, (8), 372-373.

Scopus Eid


  • 2-s2.0-2742514642

Web Of Science Accession Number


Start Page


  • 372

End Page


  • 373

Issue


  • 8