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0010372191
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2. For a partial compilation of other oxazole-containing natural products, see: Wipf, P.; Venkatraman, S. Synlett 1997, 1.
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Wipf, P.1
Venkatraman, S.2
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3
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0028866791
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3. Hennoxazole A: Wipf, P.; Lim, S. J. Am. Chem, Soc. 1995, 117, 558; Wipf, P.; Lim, S. Chimia 1996, 50, 157. Muscoride A: Wipf, P.; Venkatraman, S. J. Org. Chem. 1996, 61, 6517.
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Hennoxazole, A.1
Wipf, P.2
Lim, S.3
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4
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0001620021
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3. Hennoxazole A: Wipf, P.; Lim, S. J. Am. Chem, Soc. 1995, 117, 558; Wipf, P.; Lim, S. Chimia 1996, 50, 157. Muscoride A: Wipf, P.; Venkatraman, S. J. Org. Chem. 1996, 61, 6517.
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Wipf, P.1
Lim, S.2
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5
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0029847930
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3. Hennoxazole A: Wipf, P.; Lim, S. J. Am. Chem, Soc. 1995, 117, 558; Wipf, P.; Lim, S. Chimia 1996, 50, 157. Muscoride A: Wipf, P.; Venkatraman, S. J. Org. Chem. 1996, 61, 6517.
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Muscoride, A.1
Wipf, P.2
Venkatraman, S.3
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6
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0001470186
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4. To date, there have been three publications concerning synthetic approaches to diazonamide A: (a) Moody, C. J.; Doyle, K. J.; Elliott, M. C.; Mowlem, T. J. Pure Appl. Chem. 1994, 66, 2107.
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Doyle, K.J.2
Elliott, M.C.3
Mowlem, T.J.4
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7
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0002070317
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(b) Konopelski, J. P.; Hottenroth, J. M.; Oltra, H. M.; Veliz, E. A.; Yang, Z.-C. Synlett 1996, 609.
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Konopelski, J.P.1
Hottenroth, J.M.2
Oltra, H.M.3
Veliz, E.A.4
Yang, Z.-C.5
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33748670798
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(c) Moody, C. J.; Doyle, K. J.; Elliott, M. C.; Mowlem, T. J. J. Chem. Soc. Perkin Trans. 1 1997, 16, 2413.
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Moody, C.J.1
Doyle, K.J.2
Elliott, M.C.3
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0000980557
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5. Oikawa, Y.; Yoshida, T.; Mohri, K.; Yonemitsu, O. Heterocycles 1979, 12, 1457.
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0000121118
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6. Somei, M.; Yamada, F.; Kunimoto, M.; Kaneko, C. Heterocycles 1984, 22, 797.
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Somei, M.1
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0020455349
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and references cited therein
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7. Takuma, S.; Hamada, Y.; Shioiri, T. Chem. Pharm. Bull. 1982, 30, 3147, and references cited therein.
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Takuma, S.1
Hamada, Y.2
Shioiri, T.3
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13
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0010730490
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We thank Dr. S. Lim for preliminary studies on the preparation of oxazole 7
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9. We thank Dr. S. Lim for preliminary studies on the preparation of oxazole 7.
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14
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0010690295
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-
equation presented
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10. Wollett, G. H.; Davis, F. M.; Jones, C. N.; Neill, M. J. Am. Chem. Soc. 1937, 59, 861. (equation presented)
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Wollett, G.H.1
Davis, F.M.2
Jones, C.N.3
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17
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0000340061
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(c) Farina, V.; Kapadia, S.; Krishnan, B.; Wang, C.; Liebeskind, L. S. J. Org. Chem. 1994, 59, 5905.
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Farina, V.1
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Liebeskind, L.S.5
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18
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84985200990
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12. Maccarone, E.; Mamo, A.; Perrini, G.; Torre, M. J. Heterocyclic Chem. 1981, 18, 395.
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Maccarone, E.1
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19
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0030995738
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13. For recent reviews, see: (a) Shibasaki, M.; Boden, C. D. J.; Kojima, A. Tetrahedron 1997, 53, 7371.
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(1997)
Tetrahedron
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Shibasaki, M.1
Boden, C.D.J.2
Kojima, A.3
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20
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-
33748647785
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(b) de Meijere, A.; Meyer, F. E. Angew. Chem., Int. Ed. Engl. 1994, 33, 2379. For a related benzofuranone cyclization, see: Anacardio, R.; Arcadi, A.; D'Anniballe, G.; Marinelli, F. Synthesis 1995, 831.
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Angew. Chem., Int. Ed. Engl.
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De Meijere, A.1
Meyer, F.E.2
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21
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0029146751
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(b) de Meijere, A.; Meyer, F. E. Angew. Chem., Int. Ed. Engl. 1994, 33, 2379. For a related benzofuranone cyclization, see: Anacardio, R.; Arcadi, A.; D'Anniballe, G.; Marinelli, F. Synthesis 1995, 831.
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(1995)
Synthesis
, pp. 831
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Anacardio, R.1
Arcadi, A.2
D'Anniballe, G.3
Marinelli, F.4
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22
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0010647216
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Enantiomeric excess was determined by chiral HPLC of the O-MTPA-ester or the free alcohol derivative of 12 on a Chiralcel OD column
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14. Enantiomeric excess was determined by chiral HPLC of the O-MTPA-ester or the free alcohol derivative of 12 on a Chiralcel OD column.
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23
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0011404010
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15. Takaya, H.; Mashima, K.; Koyano, K.; Yagi, M.; Kumobayashi, H.; Taketani, T.; Akutagawa, S.; Noyori, R. J. Org. Chem. 1986, 51, 629.
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Kumobayashi, H.5
Taketani, T.6
Akutagawa, S.7
Noyori, R.8
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25
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0001518473
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17. Hayashi, T.; Mise, T.; Fukushima, M.; Kagotani, M.; Nagashima, N.; Hamada, Y.; Matsumoto, A.; Kawakami, S.; Konishi, M.; Yamamoto, K.; Kumada, M. Bull. Chem. Soc. Jpn. 1980, 53, 1138.
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Hayashi, T.1
Mise, T.2
Fukushima, M.3
Kagotani, M.4
Nagashima, N.5
Hamada, Y.6
Matsumoto, A.7
Kawakami, S.8
Konishi, M.9
Yamamoto, K.10
Kumada, M.11
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26
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33845280789
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18. Hayashi, T.; Matsumoto, Y.; Ito, Y. J. Am. Chem. Soc. 1988, 110, 5579.
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Hayashi, T.1
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Ito, Y.3
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27
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0030972808
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We thank Prof. Shibasaki for a sample of (S)-BINAs
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19. Kojima, A.; Boden, C. D. J.; Shibasaki, M. Tetrahedron Lett. 1997, 38, 3459. We thank Prof. Shibasaki for a sample of (S)-BINAs.
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Tetrahedron Lett.
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Kojima, A.1
Boden, C.D.J.2
Shibasaki, M.3
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28
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0010646691
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-
13C NMR, IR and HRMS
-
13C NMR, IR and HRMS.
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29
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0010647587
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4: (equation presented)
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4: (equation presented)
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