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1
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0026783681
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(a) Leet, J. E.; Schroeder, D. R.; Hofstead, S. J.; Golik, J.; Colson, K. L.; Huang, S.; Klohr, S. E.; Doyle, T. W.; Matson, J. A. J. Am. Chem. Soc. 1992, 114, 7946.
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Klohr, S.E.7
Doyle, T.W.8
Matson, J.A.9
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2
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0027381453
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(b) Leet, J. E.; Schroeder, D. R.; Langley, D. R.; Colson, K. L.; Huang, S.; Klohr, S. E.; Lee, M. S.; Golik, J.; Hofstead, S. J.; Doyle, T. W.; Matson, J. A. J. Am. Chem. Soc. 1993, 115, 8432.
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Leet, J.E.1
Schroeder, D.R.2
Langley, D.R.3
Colson, K.L.4
Huang, S.5
Klohr, S.E.6
Lee, M.S.7
Golik, J.8
Hofstead, S.J.9
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3
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Kawata, S.1
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4
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(a) Myers, A. G.; Goldberg, S. D. Angew. Chem., Int. Ed. 2000, 39, 2732.
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Myers, A.G.1
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(c) Myers, A. G.; Hurd, A. R.; Hogan, P. C. J. Am. Chem. Soc. 2002, 124, 4583.
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Myers, A.G.1
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7
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(a) Zhou, P.; Chen, B.-C.; Davis, F. A. Tetrahedron 2004, 60, 8003.
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Zhou, P.1
Chen, B.-C.2
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34247888167
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Ph.D. Thesis, Harvard University, Cambridge, MA
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(b) Hogan, P. C. Ph.D. Thesis, Harvard University, Cambridge, MA, 2004.
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Hogan, P.C.1
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15
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0041350417
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For examples of stereoselective (cis) palladium-mediated coupling reactions of 1,1-dihaloolefins, see: Shi, J.-C, Zeng, X, Negishi, E.-I. Org. Lett. 2003, 5, 1825 and pertinent references therein
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For examples of stereoselective (cis) palladium-mediated coupling reactions of 1,1-dihaloolefins, see: Shi, J.-C.; Zeng, X.; Negishi, E.-I. Org. Lett. 2003, 5, 1825 and pertinent references therein.
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16
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0037078348
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Shiina, I.; Kubota, M.; Ibuka, R. Tetrahedron Lett. 2002, 43, 7535.
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Shiina, I.1
Kubota, M.2
Ibuka, R.3
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Sato, I.; Akahori, Y.; Iida, K.-i.; Hirama, M. Tetrahedron Lett. 1996, 37, 5135.
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Sato, I.1
Akahori, Y.2
Iida, K.-I.3
Hirama, M.4
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19
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34247851506
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Intermediates 10-13, 15, 16, and synthetic 1 were unstable in neat form. For this reason, these compounds (when stored) were maintained in dilute solution. Yields were determined using an internal standard (see Supporting Information).
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Intermediates 10-13, 15, 16, and synthetic 1 were unstable in neat form. For this reason, these compounds (when stored) were maintained in dilute solution. Yields were determined using an internal standard (see Supporting Information).
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20
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49249151283
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Rossiter, B. E.; Verhoeven, T. R.; Sharpless, K. B. Tetrahedron Lett. 1979, 20, 4733.
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Rossiter, B.E.1
Verhoeven, T.R.2
Sharpless, K.B.3
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22
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34247856496
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14 was prepared from the commercial tartrate salt of Tylosin (three steps)
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Thioglycoside 14 was prepared from the commercial tartrate salt of Tylosin (three steps). See Supporting Information for details.
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See Supporting Information for details
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Thioglycoside1
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23
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0035793681
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Lear, M. J.; Yoshimura, F.; Hirama, M. Angew. Chem., Int. Ed. 2001, 40, 946.
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Lear, M.J.1
Yoshimura, F.2
Hirama, M.3
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24
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0026670459
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The relative and absolute stereochemistries of the kedarose, mycarose, and β-azatyrosine residues of kedarcidin chromophore have been rigorously standards. See refs lb, 2, and: Leet, J. E.; Golik, J.; Hofstead, S. J.; Matson, J. A.; Lee, A. Y.; Clardy, J. Tetrahedron Lett. 1992, 33, 6107.
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The relative and absolute stereochemistries of the kedarose, mycarose, and β-azatyrosine residues of kedarcidin chromophore have been rigorously standards. See refs lb, 2, and: Leet, J. E.; Golik, J.; Hofstead, S. J.; Matson, J. A.; Lee, A. Y.; Clardy, J. Tetrahedron Lett. 1992, 33, 6107.
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25
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0037090388
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(a) Comin, M. J.; Leitofuter, J.; Rodríguez, J. B. Tetrahedron 2002, 58, 3129.
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(2002)
Tetrahedron
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Comin, M.J.1
Leitofuter, J.2
Rodríguez, J.B.3
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26
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(b) Bickley, J. F.; Roberts, S. M.; Santoro, M. G.; Snape, T. J. Tetrahedron 2004, 60, 2569.
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(2004)
Tetrahedron
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Bickley, J.F.1
Roberts, S.M.2
Santoro, M.G.3
Snape, T.J.4
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