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Volumn 62, Issue 21, 1997, Pages 7430-7434

An efficient route to β-D-isoxazolidinyl nucleosides via diastereoselective Michael addition of hydroxylamine to unsaturated esters

Author keywords

[No Author keywords available]

Indexed keywords

BETA ISOXAZOLIDINYL NUCLEOSIDE; HYDROXYLAMINE; NUCLEOSIDE DERIVATIVE; PURINE NUCLEOSIDE; PYRIMIDINE NUCLEOSIDE; UNCLASSIFIED DRUG;

EID: 0030734550     PISSN: 00223263     EISSN: None     Source Type: Journal    
DOI: 10.1021/jo9710588     Document Type: Article
Times cited : (61)

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    • Submitted for publication
    • Compound 3 was produced in low ee by using the dipolar cycloaddition of various chiral synthons to vinylthymme. A method for the oxidative conversion of the optically active isoxazolidines to isoxazoline derivatives such as 3 has, however, been developed: Pan, L.; Gi, H.; Zhao, K. J. Org. Chem. Submitted for publication.
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    • 12a Broadly separated chemical shifts were also observed in the methylene groups of the cis isoxazolidines such as 16, 19, and 24.
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