Abstract
The iodocarbocyclization of allylmalonate using (-)-8-phenylmenthol as a chiral auxiliary proceeded with high diastereoselectivity to give the iodomethylcyclopropane dicarboxylic ester in good yield.
| Original language | English |
|---|---|
| Pages (from-to) | 691-692 |
| Number of pages | 2 |
| Journal | Tetrahedron: Asymmetry |
| Volume | 6 |
| Issue number | 3 |
| DOIs | |
| Publication status | Published - 1995 Mar |
ASJC Scopus subject areas
- Catalysis
- Physical and Theoretical Chemistry
- Organic Chemistry
- Inorganic Chemistry
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Inoue, T., Kitagawa, O., Ochiai, O., & Taguchi, T. (1995). Diastereoselective iodocarbocyclization reaction of 8-phenylmenthyl allylmalonate: An efficient preparation of a synthetic intermediate of cyclopropane amino acids. Tetrahedron: Asymmetry, 6(3), 691-692. https://doi.org/10.1016/0957-4166(95)00063-U