Abstract
Reformatsky-type additions, under various metal-mediated activation, of ethyl bromodifluoroacetate toward a series of unactivated lactones and various sugar lactones proceeded with medium to good yields and in a completely diastereoselective manner.
Original language | English |
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Article number | G26505ST |
Pages (from-to) | 2627-2630 |
Number of pages | 4 |
Journal | Synlett |
Issue number | 17 |
DOIs | |
Publication status | Published - 17 Oct 2005 |
Externally published | Yes |
Keywords
- Addition reactions
- Carbohydrates
- Fluorine
- Lactones
- Stereoselectivity