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D'Ambrosio, M.1
Guerriero, A.2
Debitus, C.3
Pietra, F.4
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2
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0011738567
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note
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Subsequent samples of the sponge did not contain leucascandrolide A, strongly suggesting the microbial origin of this natural product.
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3
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0034722988
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(a) Hornberger, K. R.; Hamblett, C. L.; Leighton, J. L. J. Am. Chem. Soc. 2000, 122, 12894.
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Hornberger, K.R.1
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5
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(c) Crimmins, M. T.; Carroll, C. A.; King, B. W. Org. Lett. 2000, 2, 597.
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Crimmins, M.T.1
Carroll, C.A.2
King, B.W.3
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9
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0001767306
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For formation of 1.3-dioxanes via Lewis acid or Bronsted acid-catalyzed macrotransacetalization, see: Still, W. C.; Li, G. J. Am. Chem. Soc. 1993, 115, 3804. (b) Wender, P. A.; Brabander, J. D.; Harran, P. G.; Jimenez, J. M.; Koehler, M. F. T.; Lippa, B.; Park, C. M.; Shiozaki, M. J. Am. Chem. Soc. 1998, 120, 4534.
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Still, W.C.1
Li, G.2
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10
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0032513707
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For formation of 1.3-dioxanes via Lewis acid or Bronsted acid-catalyzed macrotransacetalization, see: Still, W. C.; Li, G. J. Am. Chem. Soc. 1993, 115, 3804. (b) Wender, P. A.; Brabander, J. D.; Harran, P. G.; Jimenez, J. M.; Koehler, M. F. T.; Lippa, B.; Park, C. M.; Shiozaki, M. J. Am. Chem. Soc. 1998, 120, 4534.
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Wender, P.A.1
Brabander, J.D.2
Harran, P.G.3
Jimenez, J.M.4
Koehler, M.F.T.5
Lippa, B.6
Park, C.M.7
Shiozaki, M.8
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11
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0027180369
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For cyanation of alkynyl zincs, see: Klement, I.; Lennick, K.; Tucker, C. E.; Knochel, P. Tetrahedron Lett. 1993, 34, 4623. For cyanation of lithium enolates, see: Kahne, D.; Collum, D. B. Tetrahedron Lett. 1981, 22, 5011.
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Klement, I.1
Lennick, K.2
Tucker, C.E.3
Knochel, P.4
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12
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0000814872
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For cyanation of alkynyl zincs, see: Klement, I.; Lennick, K.; Tucker, C. E.; Knochel, P. Tetrahedron Lett. 1993, 34, 4623. For cyanation of lithium enolates, see: Kahne, D.; Collum, D. B. Tetrahedron Lett. 1981, 22, 5011.
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Kahne, D.1
Collum, D.B.2
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13
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18444417883
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and reference cited therein
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(a) Doyle, M. P. Chem. Rev. 1986, 86, 919 and reference cited therein.
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Doyle, M.P.1
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14
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0023005472
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(b) Connell, R. D.; Scavo, F.; Helquist, P.; Åkermark, B. Tetrahedron Lett, 1986, 27, 5559.
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Connell, R.D.1
Scavo, F.2
Helquist, P.3
Åkermark, B.4
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16
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0011706538
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For details, see the Supporting Information
-
For details, see the Supporting Information.
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17
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0011742376
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note
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8
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18
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0011766181
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note
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7.
-
-
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19
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0011765301
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note
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17 epimeric triol 19 to the oxidative cleavage conditions resulted only in formation of the corresponding hydroxy aldehyde 20.
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20
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0000192963
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(a) Oikawa, Y.; Yoshioka, T.; Yonemitsu, O. Tetrahedron Lett. 1982, 23, 885.
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Oikawa, Y.1
Yoshioka, T.2
Yonemitsu, O.3
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