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Volumn 4, Issue 2, 2002, Pages 301-303

Highly diastereoselective reformatsky-type reaction promoted by tin iodide Ate complex

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ARTICLE;

EID: 0141663487     PISSN: 15237060     EISSN: None     Source Type: Journal    
DOI: 10.1021/ol0171214     Document Type: Article
Times cited : (24)

References (29)
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    • 1H NMR in comparison with the stereochemically defined authentic samples.
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    • For example, see: (a) Davis, A. G. Organotin Chemistry; VCH: New York, 1997; pp 18. (b) Harrison, P. G. Chemistry of Tin; Blackie; London, 1989; p 71. (c) Holecek, J.; Nádvorník, M.; Handlír, K.; Lycka, A. J. Organomet. Chem. 1983, 241, 177. (d) Nádvorník, M.; Holecek, J.; Handlír, K.; Lycka, A. J. Organomet. Chem. 1984, 275, 43.
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    • note
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    • 2e although no homocoupling products of haloketones or aldehydes have been obtained
    • 2e although no homocoupling products of haloketones or aldehydes have been obtained.


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