A Useful Method for the Selective Reduction of Isoxazoline Nuclei in the Presence of Double Bonds by the Use of Lindlar Catalyst

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Natural Product Synthesis Through Pericyclic Reaction Desmoni, G.;Tacconi, G.;Baro, A.;Pollini, G. P.
Acc. Chem. Res. v.17 Kozikowski, A. P.
Advances in Cycloaddition v.1 Curran, D. P.;Curran, D. P.(ed.)
Acta Chem. Scand. Ser. B v.32 Torssell, K. B. G.;Zeuthen, O.
Synthesis Wollenberg, R. H.;Goldstein, J. E.
Tetrahedron Lett. v.23 Kozikowski, A. P.;Adamczyk, M.
Tetrahedron Lett. v.24 Martin, S. F.;Dupre, B.
J. Am. Chem. Soc. v.104 Curran, D. P.
J. Am. Chem. Soc. v.105 Curran, D. P.
Acta Chem. Scand. Ser. B v.36 Anderson, S. H.;Das, B. D.;Jorgenson, R. D.;Kjeldsen, G.;Knudsen, J. S.;Sharma, S. C.;Torssell. K. B. G.
J. Basic Sci. Sungshin v.11 Kim, S. O.;Sa, W. H.;Lee, E. K.
Ph. D. Thesis, University of Pittsburgh Jung, S. H.
Synthesis Lee, G. A.
J. Org. Chem. v.43 Mancuso, A. J.;Huang, S.-L.;Swern, D.

ChemInform Abstract: A Useful Method for the Selective Reduction of Isoxazoline Nuclei in the Presence of Double Bonds by the Use of Lindlar Catalyst. vol.27, pp.30, 1996, https://doi.org/10.1002/chin.199630082
Stereocontrolled formation of highly substituted cis-decalins via INOC annulation. An access to the branimycin core vol.63, pp.26, 2007, https://doi.org/10.1016/j.tet.2007.02.126
Total Synthesis of Branimycin: An Evolutionary Approach vol.18, pp.31, 1996, https://doi.org/10.1002/chem.201200257