Dipolar cycloaddition / Nitrile oxides / CฯชO bond cleavage / Nitro alkenes An enantioselective synthesis of N-protected amino diols has Subsequent diastereo-and regioselective cycloaddition reactions to highly substituted 4,5-isoxazolines 5a-e, 8a, b been accomplished by employing a diastereoselect
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ChemInform Abstract: Diastereo- and Enantioselective Synthesis of N-Protected 2-Amino 1,4-Diols by an Oxa Michael Addition/1,3-Dipolar Cycloaddition Protocol.
โ Scribed by D. ENDERS; A. HAERTWIG; J. RUNSINK
- Publisher
- John Wiley and Sons
- Year
- 2010
- Weight
- 34 KB
- Volume
- 30
- Category
- Article
- ISSN
- 0931-7597
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