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Bach T, Bergmann H, Grosch B, et al. Highly enantioselective intra- and intermolecular [2 + 2] photocycloaddition reactions of 2-quinolones mediated by a chiral lactam host: host-guest interactions, product configuration, and the origin of the stereoselectivity in solution. J Am Chem Soc. 2002;124(27):7982-90doi: 10.1021/ja0122288.
Bach, T., Bergmann, H., Grosch, B., & Harms, K. (2002). Highly enantioselective intra- and intermolecular [2 + 2] photocycloaddition reactions of 2-quinolones mediated by a chiral lactam host: host-guest interactions, product configuration, and the origin of the stereoselectivity in solution. Journal of the American Chemical Society, 124(27), 7982-90. https://doi.org/10.1021/ja0122288
Bach, Thorsten, et al. "Highly enantioselective intra- and intermolecular [2 + 2] photocycloaddition reactions of 2-quinolones mediated by a chiral lactam host: host-guest interactions, product configuration, and the origin of the stereoselectivity in solution." Journal of the American Chemical Society vol. 124,27 (2002): 7982-90. doi: https://doi.org/10.1021/ja0122288
Bach T, Bergmann H, Grosch B, Harms K. Highly enantioselective intra- and intermolecular [2 + 2] photocycloaddition reactions of 2-quinolones mediated by a chiral lactam host: host-guest interactions, product configuration, and the origin of the stereoselectivity in solution. J Am Chem Soc. 2002 Jul 10;124(27):7982-90. doi: 10.1021/ja0122288. PMID: 12095342.
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