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Li, T.10
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and references cited therein
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For a comprehensive review on the chemistry and biology of the sarcodictyins, see: (a) Nicolaou, K. C.; Pfefferkorn, J.; Xu, J.; Winssinger, N.; Ohshima, T.; Kim, S.; Hosokawa, S.; Vourloumis, D.; van Delft, F.; Li, T. Chem. Pharm. Bull. 1999, 47, 1199. See also: (b) Nicolaou, K. C.; Winssinger, N.; Vorloumis, D.; Ohshima, T.; Kim, S.; Pfefferkorn, J.; Xu, J. Y.; Li, T. J. Am. Chem. Soc. 1998, 120, 10814; (c) Britton, R.; de Silva, E. D.; Bigg, C. M.; McHardy, L. M.; Roberge, M.; Andersen, R. J. J. Am. Chem. Soc. 2001, 123, 8632 and references cited therein.
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For reviews, see: (a) Grubbs, R. H.; Chang, S. Tetrahedron 1998, 54, 4413; (b) Armstrong, S. K. J. Chem. Soc., Perkin Trans. 1 1998, 371; (c) Maier, M. E. Angew. Chem., Int. Ed. 2000, 39, 2073; (d) Fürstner, A. Angew. Chem., Int. Ed. 2000, 39, 3012.
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For reviews, see: (a) Grubbs, R. H.; Chang, S. Tetrahedron 1998, 54, 4413; (b) Armstrong, S. K. J. Chem. Soc., Perkin Trans. 1 1998, 371; (c) Maier, M. E. Angew. Chem., Int. Ed. 2000, 39, 2073; (d) Fürstner, A. Angew. Chem., Int. Ed. 2000, 39, 3012.
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Armstrong, S.K.1
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For reviews, see: (a) Grubbs, R. H.; Chang, S. Tetrahedron 1998, 54, 4413; (b) Armstrong, S. K. J. Chem. Soc., Perkin Trans. 1 1998, 371; (c) Maier, M. E. Angew. Chem., Int. Ed. 2000, 39, 2073; (d) Fürstner, A. Angew. Chem., Int. Ed. 2000, 39, 3012.
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Maier, M.E.1
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0032580376
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For reviews, see: (a) Grubbs, R. H.; Chang, S. Tetrahedron 1998, 54, 4413; (b) Armstrong, S. K. J. Chem. Soc., Perkin Trans. 1 1998, 371; (c) Maier, M. E. Angew. Chem., Int. Ed. 2000, 39, 2073; (d) Fürstner, A. Angew. Chem., Int. Ed. 2000, 39, 3012.
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Fürstner, A.1
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34
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0013017337
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13C NMR, IR) completely in accord with their assigned structures. Details will be provided in a subsequent full paper.
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13C NMR, IR) completely in accord with their assigned structures. Details will be provided in a subsequent full paper.
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-
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35
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0035813926
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Application of the RCM reaction to ten-membered carbocycles is still very rare, see: (a) Nevalainen, M.; Koskinen, A. M. P. Angew. Chem., Int. Ed. 2001, 40, 4060; J. Org. Chem. 2002, 67, 1554; (b) Ref. 5h.
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Angew. Chem., Int. Ed.
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Nevalainen, M.1
Koskinen, A.M.P.2
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36
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0037040699
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Application of the RCM reaction to ten-membered carbocycles is still very rare, see: (a) Nevalainen, M.; Koskinen, A. M. P. Angew. Chem., Int. Ed. 2001, 40, 4060; J. Org. Chem. 2002, 67, 1554; (b) Ref. 5h.
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37
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0035813926
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Ref. 5h
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Application of the RCM reaction to ten-membered carbocycles is still very rare, see: (a) Nevalainen, M.; Koskinen, A. M. P. Angew. Chem., Int. Ed. 2001, 40, 4060; J. Org. Chem. 2002, 67, 1554; (b) Ref. 5h.
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38
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0037134804
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The use of 'second generation' metathesis catalysts results in the selective formation of the thermodynamically favored stereoisomeric products in RCM reactions furnishing medium-sized rings, see: (a) Fürstner, A.; Radkowski, K.; Wirtz, C.; Goddard, R.; Lehmann, C. W.; Mynott, R. J. Am. Chem. Soc. 2002, 124, 7061; (b) Murga, J.; Falomir, E.; Garcìa-Fortanet, J.; Carda, M.; Marco, J. A. Org. Lett. 2002, 4, 3447.
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Radkowski, K.2
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Goddard, R.4
Lehmann, C.W.5
Mynott, R.6
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39
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0037015429
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The use of 'second generation' metathesis catalysts results in the selective formation of the thermodynamically favored stereoisomeric products in RCM reactions furnishing medium-sized rings, see: (a) Fürstner, A.; Radkowski, K.; Wirtz, C.; Goddard, R.; Lehmann, C. W.; Mynott, R. J. Am. Chem. Soc. 2002, 124, 7061; (b) Murga, J.; Falomir, E.; Garcìa-Fortanet, J.; Carda, M.; Marco, J. A. Org. Lett. 2002, 4, 3447.
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Murga, J.1
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Carda, M.4
Marco, J.A.5
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For discussions on the role of allylic oxygen substituents in the RCM reaction, see: (a) White, J. D.; Hrnciar, P. J. Org. Chem. 2000, 65, 9129; (b) Paquette, L. A.; Efremov, I. J. Am. Chem. Soc. 2001, 123, 4492; (c) Maishal, T. K.; Sinha-Mahapatra, D. K.; Paranjape, K.; Sarkar, A. Tetrahedron Lett. 2002, 43, 2263.
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Hrnciar, P.2
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43
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For discussions on the role of allylic oxygen substituents in the RCM reaction, see: (a) White, J. D.; Hrnciar, P. J. Org. Chem. 2000, 65, 9129; (b) Paquette, L. A.; Efremov, I. J. Am. Chem. Soc. 2001, 123, 4492; (c) Maishal, T. K.; Sinha-Mahapatra, D. K.; Paranjape, K.; Sarkar, A. Tetrahedron Lett. 2002, 43, 2263.
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Paquette, L.A.1
Efremov, I.2
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44
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0037128527
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for discussions on the role of allylic oxygen substituents in the RCM reaction, see: (a) White, J. D.; Hrnciar, P. J. Org. Chem. 2000, 65, 9129; (b) Paquette, L. A.; Efremov, I. J. Am. Chem. Soc. 2001, 123, 4492; (c) Maishal, T. K.; Sinha-Mahapatra, D. K.; Paranjape, K.; Sarkar, A. Tetrahedron Lett. 2002, 43, 2263.
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Maishal, T.K.1
Sinha-Mahapatra, D.K.2
Paranjape, K.3
Sarkar, A.4
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