Abstract
Racemicendo-5-acetyl-1,2,3,4-tetrachloro-7,7-dimethoxynorborn-2-ene was stereoselectively reduced by sodium borohydride to give only theS,S orR,R diastereomers. The crystal structure of the product displays no unusual features.
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Bott, S.G., Marchand, A.P., Bolin, J. et al. Highly stereoselective sodium borohydride promoted reduction ofendo-5-acetyl-1,2,3,4-tetrachloro-7,7-dimethoxynorborn-2-ene. J Chem Crystallogr 25, 657–660 (1995). https://doi.org/10.1007/BF01665972
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DOI: https://doi.org/10.1007/BF01665972