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1
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0141742509
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For recent reviews on this family of natural products, see: a
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For recent reviews on this family of natural products, see: (a) Hoffman, H.; Lindel, T. Synthesis 2003, 12, 1753.
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Hoffman, H.1
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O'Malley, D. P.; Yamaguchi, J.; Young, I. S.; Seiple, I. B.; Baran, P. S. Angew. Chem., Int. Ed. 2008, 47, 3581.
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O'Malley, D.P.1
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Young, I.S.3
Seiple, I.B.4
Baran, P.S.5
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4
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35048820403
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For recent advances toward oroidin alkaloids not cited in ref 1 see: a
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For recent advances toward oroidin alkaloids not cited in ref 1 see: (a) Sivappa, R.; Hernandez, N. M.; He, Y.; Lovely, C. J. Org. Lett. 2007, 9, 3861-3864.
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(b) Lanman, B. A.; Overman, L. E.; Paulini, R.; White, N. S. J. Am. Chem. Soc. 2007, 129, 12896.
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Lanman, B.A.1
Overman, L.E.2
Paulini, R.3
White, N.S.4
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6
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34247515502
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(c) O'Malley, D. P.; Li, K.; Maue, M.; Zografos, A. L.; Baran, P. S. J. Am. Chem. Soc. 2007, 129, 4762.
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(2007)
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O'Malley, D.P.1
Li, K.2
Maue, M.3
Zografos, A.L.4
Baran, P.S.5
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7
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33746288746
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(d) Tan, X.; Chen, C. Angew. Chem., Int. Ed. 2006, 45, 4345.
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Tan, X.1
Chen, C.2
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8
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(e) Wang, S.; Dilley, A. S.; Poullennec, K. G.; Romo, D. Tetrahedron 2006, 62, 7155.
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(2006)
Tetrahedron
, vol.62
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Wang, S.1
Dilley, A.S.2
Poullennec, K.G.3
Romo, D.4
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9
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13444252897
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(f) Garrido-Hernandez, H.; Nakadai, M.; Vimolratana, M.; Li, Q.; Doundoulakis, T.; Harran, P. G. Angew. Chem., Int. Ed. 2005, 44, 765.
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Garrido-Hernandez, H.1
Nakadai, M.2
Vimolratana, M.3
Li, Q.4
Doundoulakis, T.5
Harran, P.G.6
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10
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34249278061
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(a) Buchanan, M. S.; Carroll, R.; Quinn, R. J. Tetrahedron Lett. 2007, 48, 4573.
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Buchanan, M.S.1
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(b) Buchanan, M. S.; Carroll, R.; Addepalli, R.; Avery, V. M.; Hooper, J. N. A.; Quinn, R. J. J. Org. Chem. 2007, 72, 2309.
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(c) Grube, A.; Köck, M. Angew. Chem., Int. Ed. 2007, 46, 2320.
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Grube, A.1
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(d) Kobayashi, H.; Kitamura, K.; Nagai, K.; Nakao, Y.; Fusetani, N.; van Soest, R. W. M.; Matsunaga, S. Tetrahedron Lett. 2007, 48, 2127.
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Kobayashi, H.1
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van Soest, R.W.M.6
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and references cited therein
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(c) Keese, R. Angew. Chem., Int. Ed. 1992, 31, 344, and references cited therein.
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23
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0001324068
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To the best of our knowledge Mori was the first to report the synthesis of this system, see
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To the best of our knowledge Mori was the first to report the synthesis of this system, see: Mori, M.; Saitoh, F.; Uesaka, N.; Okamura, K.; Date, T. J. Org. Chem. 1994, 59, 4993.
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J. Org. Chem
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Date, T.5
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24
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34548640751
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Köck, M.; Grube, A.; Seiple, I. B.; Baran, P. S. Angew. Chem., Int. Ed. 2007, 46, 6586.
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Köck, M.1
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41249086158
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Wang, S.; Romo, D. Angew. Chem., Int. Ed. 2008, 47, 1284.
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Angew. Chem., Int. Ed
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Wang, S.1
Romo, D.2
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27
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33744984312
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(a) Dransfield, P. J.; Dilley, A. S.; Wang. S.; Romo, D. Tetrahedron 2006, 62, 5223.
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Dransfield, P.J.1
Dilley, A.S.2
Wang, S.3
Romo, D.4
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29
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61349181687
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Full details of the extensive studies leading to optimization of this ring cleavage/epimerjzation of β-lactam 7 to deliver ester 8 will be described in a separate report
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Full details of the extensive studies leading to optimization of this ring cleavage/epimerjzation of β-lactam 7 to deliver ester 8 will be described in a separate report.
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30
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61349115368
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4 enabled complete conversion to the desired alcohol.
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4 enabled complete conversion to the desired alcohol.
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31
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34249278061
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Buchanan, M. S.; Carroll, A. R.; Quinn, R. J. Tetrahedron Lett. 2007, 48, 4573.
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(2007)
Tetrahedron Lett
, vol.48
, pp. 4573
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Buchanan, M.S.1
Carroll, A.R.2
Quinn, R.J.3
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32
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0037863192
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For a related example of over-oxidation during PMB removal, see
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For a related example of over-oxidation during PMB removal, see: Ohfune, Y.; Demura, T.; Iwama, S.; Matsuda, H.; Namba, K.; Shimamoto, K.; Shinada, T. Tetrahedron Lett. 2003, 44, 5431.
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(2003)
Tetrahedron Lett
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, pp. 5431
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Ohfune, Y.1
Demura, T.2
Iwama, S.3
Matsuda, H.4
Namba, K.5
Shimamoto, K.6
Shinada, T.7
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33
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61349113206
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While our work was in progress, Baran and co-workers also reported the facility of this cyclization in the course of their studies leading to axinellamine see ref 2
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While our work was in progress, Baran and co-workers also reported the facility of this cyclization in the course of their studies leading to axinellamine (see ref 2).
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