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6
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0000623741
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Total synthesis of (+)-ryanodol was accomplished by Deslongchamps et al. (a)
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Total synthesis of (+)-ryanodol was accomplished by Deslongchamps et al. (a) A. Bélanger, D.J.F. Berney, H.-J. Borschberg, R. Brousseau, A. Doutheau, R. Durand, H. Katayama, R. Lapalme, D.M. Leturc, C.-C. Liao, F.N. MacLachlan, J.-P. Maffrand, F. Marazza, R. Martino, C. Moreau, L. Saint-Laurent, R. Saintonge, P. Soucy, L. Ruest, and P. Deslongchamps Can. J. Chem. 57 1979 3348
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Bélanger, A.1
Berney, D.J.F.2
Borschberg, H.-J.3
Brousseau, R.4
Doutheau, A.5
Durand, R.6
Katayama, H.7
Lapalme, R.8
Leturc, D.M.9
Liao, C.-C.10
Maclachlan, F.N.11
Maffrand, J.-P.12
Marazza, F.13
Martino, R.14
Moreau, C.15
Saint-Laurent, L.16
Saintonge, R.17
Soucy, P.18
Ruest, L.19
Deslongchamps, P.20
more..
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7
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references cited therein
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P. Deslongchamps, A. Bélanger, D.J.F. Berney, H.-J. Borschberg, R. Brousseau, A. Doutheau, R. Durand, H. Katayama, R. Lapalme, D.M. Leturc, C.-C. Liao, F.N. MacLachlan, J.-P. Maffrand, F. Marazza, R. Martino, C. Moreau, L. Ruest, L. Saint-Laurent, R. Saintonge, and P. Soucy Can. J. Chem. 68 1990 186 and references cited therein
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Deslongchamps, P.1
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Brousseau, R.5
Doutheau, A.6
Durand, R.7
Katayama, H.8
Lapalme, R.9
Leturc, D.M.10
Liao, C.-C.11
Maclachlan, F.N.12
Maffrand, J.-P.13
Marazza, F.14
Martino, R.15
Moreau, C.16
Ruest, L.17
Saint-Laurent, L.18
Saintonge, R.19
Soucy, P.20
more..
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8
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58149514666
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For synthetic studies of ryanodol from our laboratory, see: (a)
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For synthetic studies of ryanodol from our laboratory, see: (a) K. Hagiwara, M. Himuro, M. Hirama, and M. Inoue Tetrahedron Lett. 50 2009 1035
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Synthesis of enantiopure intermediates, see
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Synthesis of enantiopure intermediates, see M. Iwatsu, D. Urabe, and M. Inoue Heterocycles 82 2010 491
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Iwatsu, M.1
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84899580834
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We recently achieved the total synthesis of ryanodol.
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We recently achieved the total synthesis of ryanodol. M. Nagatomo, M. Koshimizu, K. Masuda, T. Tabuchi, D. Urabe, and M. Inoue J. Am. Chem. Soc. 136 2014 5916
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Symmetry-driven synthesis of the natural products from our laboratory. Merrilactone A: (a)
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Symmetry-driven synthesis of the natural products from our laboratory. Merrilactone A: (a) M. Inoue, T. Sato, and M. Hirama J. Am. Chem. Soc. 125 2003 10772
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Upon treatment with a bulky and anionic nucleophile, the 1,2-diketone moiety of 2 was prone to undergo reduction into the corresponding α-hydroxy ketone, presumably through the single electron transfer (SET) mechanism. The SET process appeared to be involved in other decomposition pathways. For related examples, see: (a)
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Upon treatment with a bulky and anionic nucleophile, the 1,2-diketone moiety of 2 was prone to undergo reduction into the corresponding α-hydroxy ketone, presumably through the single electron transfer (SET) mechanism. The SET process appeared to be involved in other decomposition pathways. For related examples, see: (a) G.B. Bennett, W.J. Houlihan, and R.B. Mason J. Organomet. Chem. 99 1975 185
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