Abstract
Additions of nucleophiles to the carbonyls of several enantiomerically pure bicyclo[m.1.0]alkan-2-ones were found to be highly diastereoselective.
| Original language | English (US) |
|---|---|
| Pages (from-to) | 4565-4568 |
| Number of pages | 4 |
| Journal | Tetrahedron Letters |
| Volume | 31 |
| Issue number | 32 |
| DOIs | |
| State | Published - 1990 |
ASJC Scopus subject areas
- Biochemistry
- Drug Discovery
- Organic Chemistry
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Mash, E. A., Kaczynski, M. A., & Dolata, D. P. (1990). Diastereoselective manipulations of conformationally restricted enantiomerically pure bicyclo[m.1.0]alkanes. 1. Nucleophilic additions to the carbonyl carbons of bicyclo[m.1.0]alkan-2-ones. Tetrahedron Letters, 31(32), 4565-4568. https://doi.org/10.1016/S0040-4039(00)97677-9