Abstract
Kinetic resolution provided a highly enantioselective method to access a range of 3-aryl-3,4-dihydro-2H-1,4-benzoxazines using n-butyllithium and the chiral ligand sparteine. The enantioenrichment remained high on removing the tert-butoxycarbonyl (Boc) protecting group. The intermediate organolithium undergoes ring opening to an enamine. The kinetic resolution was extended to give enantiomerically enriched substituted 1,2,3,4-tetrahydroquinoxalines and was applied to the synthesis of an analogue of the antibiotic levofloxacin that was screened for its activity against the human pathogen Streptococcus pneumoniae.
| Original language | English |
|---|---|
| Pages (from-to) | 355-368 |
| Number of pages | 14 |
| Journal | Synthesis (Germany) |
| Volume | 54 |
| Issue number | 2 |
| Early online date | 26 Oct 2021 |
| DOIs | |
| Publication status | Published - 2022 |
Bibliographical note
Publisher Copyright:© 2021. Thieme. All rights reserved.
Keywords
- antibiotics
- elimination
- enantioselectivity
- heterocycles
- kinetic resolution
- lithiation
- ring opening
ASJC Scopus subject areas
- Catalysis
- Organic Chemistry
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