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Volumn 61, Issue 22, 1996, Pages 7963-7966

Highly efficient and enantioselective synthesis of carbocyclic nucleoside analogs using selective early transition metal catalysis

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EID: 0039094109     PISSN: 00223263     EISSN: None     Source Type: Journal    
DOI: 10.1021/jo961241l     Document Type: Article
Times cited : (59)

References (36)
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    • 2 with the same enantioselectivity as chloride complex 2a; however, the use of azide complex 2b avoids the production of minor amounts of a chloride addition side product observed when catalyst 2a is used: Leighton, J. L.; Jacobsen, E. N. J. Org. Chem. 1996, 61, 389.
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    • For the conversion of 15 to carbovir, see ref 7e
    • For the conversion of 15 to carbovir, see ref 7e.


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