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 original | English |
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Páginas (desde-hasta) | 7727-7730 |
Número de páginas | 4 |
Publicación | Tetrahedron Letters |
Volumen | 40 |
N.º | 44 |
DOI | |
Estado | Published - oct. 29 1999 |
Publicado de forma externa | Sí |
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