Effect of a remote substituent on regioselectivity in oxymercuration of unsymmetrically substituted norbornenes

Peter Mayo, Marc Poirier, Jan Rainey, William Tam

Producción científica: Contribución a una revistaArtículorevisión exhaustiva

11 Citas (Scopus)

Resumen

The effect of a remote substituent on the regioselectivity in the oxymercuration of unsymmetrical substituted norbornenes has been investigated. Moderate to high levels of regioselectivity were observed with both exo- and endo-substituents at C-2 of norbornenes.

Idioma originalEnglish
Páginas (desde-hasta)7727-7730
Número de páginas4
PublicaciónTetrahedron Letters
Volumen40
N.º44
DOI
EstadoPublished - oct. 29 1999
Publicado de forma externa

Nota bibliográfica

Funding Information:
We thank the Natural Science and Engineering Research Council (NSERC) of Canada and the University of Guelph for the generous financial support of our program. Peter Mayo thanks NSERC for a PGS A Scholarship. Ms. Valerie Robinson is thanked for NMR experiments and discussion of NMR data.

ASJC Scopus Subject Areas

  • Biochemistry
  • Drug Discovery
  • Organic Chemistry

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