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In: Zhu J., and Beinaymé H. (Eds). Multicomponent Reactions (2005), Wiley-VCH, Weinheim
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Multi-step reactions relying upon the formation and conversion of initial reaction products to subsequent compounds have been called tandem reactions, cascade reactions, and, more recently, domino reactions. Tietze L.F., Brasche G., and Gericke K.M. (Eds), Wiley-VCH, Weinheim
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Multi-step reactions relying upon the formation and conversion of initial reaction products to subsequent compounds have been called tandem reactions, cascade reactions, and, more recently, domino reactions. In: Tietze L.F., Brasche G., and Gericke K.M. (Eds). Domino Reactions in Organic Synthesis (2006), Wiley-VCH, Weinheim
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Komatsu N. In: Suzuki H., and Matano Y. (Eds). Organobismuth Chemistry (2001), Elsevier, New York, NY 371-440
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Komatsu, N.1
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7
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67650522838
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3 is listed as 3334 mg/kg (oral, rat) and 2250 mg/kg (oral, mouse) in the MSDS provided by Sigma-Aldrich Chemical, St. Louis, MO.
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3 is listed as 3334 mg/kg (oral, rat) and 2250 mg/kg (oral, mouse) in the MSDS provided by Sigma-Aldrich Chemical, St. Louis, MO.
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9
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38849162952
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in ref. 1:. Zhu J., and Beinaymé H. (Eds), Wiley-VCH, Weinheim
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Jacques T., Markó I.E., and Pospíšil J. in ref. 1:. In: Zhu J., and Beinaymé H. (Eds). Multicomponent Reactions (2005), Wiley-VCH, Weinheim 398-452
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Jacques, T.1
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Pospíšil, J.3
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10
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67650513248
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Markó developed and has extensively examined the ISMS reaction. For representative examples, see
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Markó developed and has extensively examined the ISMS reaction. For representative examples, see:
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12
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0030914643
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25
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67650519013
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Recent reviews of synthetic methods toward a number of natural products containing cyclic ethers
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Recent reviews of synthetic methods toward a number of natural products containing cyclic ethers:
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28
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67650537990
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For a variety of methods for the synthesis of dihydropyran ring systems, see
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For a variety of methods for the synthesis of dihydropyran ring systems, see:
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40
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67650543806
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For recent examples of dihydropyran preparations involving intramolecular reactions of alkynes, see
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For recent examples of dihydropyran preparations involving intramolecular reactions of alkynes, see:
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43
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67650516712
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Prins reactions have also been used extensively in the formation of tetrahydropyrans
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Prins reactions have also been used extensively in the formation of tetrahydropyrans:
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49
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33846045231
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Panek et al. used a 2,6-disubstituted dihydropyran in their synthesis of leucascandrolide A:
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Panek et al. used a 2,6-disubstituted dihydropyran in their synthesis of leucascandrolide A:. Su Q., Dakin L.A., and Panek J.S. J. Org. Chem. 72 (2007) 2-24
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67650540711
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note
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GFS Chemical Corporation.
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53
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0141765923
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and refs. therein
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Dobbs, A.P.1
Guesne, S.J.J.2
Martinovic, S.3
Coles, S.J.4
Hursthouse, M.B.5
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54
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0000478068
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3-mediated Mukaiyama aldol reactions were first reported in 1988:
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3-mediated Mukaiyama aldol reactions were first reported in 1988:. Ohki H., Wada M., and Akiba K. Tetrahedron Lett. 29 (1988) 4719-4721
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Tetrahedron Lett.
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Le Roux C., Ciliberti L., Laurent-Robert H., Laporterie A., and Dubac J. Synlett (1998) 1249-1251
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57
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37549012873
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3-mediated vinylogous Mukaiyama aldol reaction, see:
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3-mediated vinylogous Mukaiyama aldol reaction, see:. Ollevier T., Bouchard J.-E., and Desyroy V. J. Org. Chem. 73 (2008) 331-334
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Vignaux, P.5
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60
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67650528723
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note
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See the supporting information for qualititative NOE spectra.
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67
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27144472960
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Mazières, S.1
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74
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12344333733
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3 was found to be a poor catalyst for methanesulfonylation of arenes. The authors noted a synergistic effect involving ligand exchange reactions:
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3 was found to be a poor catalyst for methanesulfonylation of arenes. The authors noted a synergistic effect involving ligand exchange reactions:. Peyronneau M., Boisdon M.-T., Roques N., Mazières S., and Le Roux C. Eur. J. Org. Chem. (2004) 4636-4640
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Peyronneau, M.1
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Le Roux, C.5
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75
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33749998087
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3 is involved as more than just a progenitor of TfOH:
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3 is involved as more than just a progenitor of TfOH:. Ollevier T., Nadeau E., and Guay-Bégin A.-A. Tetrahedron Lett. 47 (2006) 8351-8354
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76
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In cases where Brønsted and Lewis acids are present, a number of interactions are possible, including Brønsted acid assisted Lewis acid catalysts (BLA), etc. See:
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In cases where Brønsted and Lewis acids are present, a number of interactions are possible, including Brønsted acid assisted Lewis acid catalysts (BLA), etc. See:. Yamamoto H., and Futatsugi K. Angew. Chem., Int. Ed. 44 (2005) 1924-1942
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