메뉴 건너뛰기




Volumn 59, Issue 35, 2003, Pages 6899-6904

Study towards bioactive pyrone derivatives from the marine red alga Phacelocarpus labillardieri

Author keywords

Alkynes; Macrocycles; Marine natural products; Metathesis; Pyrone

Indexed keywords

CYCLOPHANE; PHOSPHOLIPASE A2; PYRONE DERIVATIVE;

EID: 0041657514     PISSN: 00404020     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0040-4020(03)00815-9     Document Type: Article
Times cited : (36)

References (64)
  • 7
    • 0037455149 scopus 로고    scopus 로고
    • For representative examples see: (a) Fürstner A., Leitner A. Angew. Chem., Int. Ed. 42:2003;308-311 (b) Fürstner A., Krause H., Thiel O.R. Tetrahedron. 58:2002;6373-6380 (c) Fürstner A., Gastner T. Org. Lett. 2:2000;2467-2470 (d) Fürstner A., Thiel O.R. J. Org. Chem. 65:2000;1738-1742 (e) Fürstner A., Grabowski J., Lehmann C.W. J. Org. Chem. 64:1999;8275-8280 (f) Fürstner A., Weintritt H. J. Am. Chem. Soc. 120:1998;2817-2825 (g) Fürstner A., Weintritt H., Hupperts A. J. Org. Chem. 60:1995;6637-6641 (h) Fürstner A., Hupperts A. J. Am. Chem. Soc. 117:1995;4468-4475.
    • (2003) Angew. Chem., Int. Ed. , vol.42 , pp. 308-311
    • Fürstner, A.1    Leitner, A.2
  • 8
    • 0037025916 scopus 로고    scopus 로고
    • For representative examples see: (a) Fürstner A., Leitner A. Angew. Chem., Int. Ed. 42:2003;308-311 (b) Fürstner A., Krause H., Thiel O.R. Tetrahedron. 58:2002;6373-6380 (c) Fürstner A., Gastner T. Org. Lett. 2:2000;2467-2470 (d) Fürstner A., Thiel O.R. J. Org. Chem. 65:2000;1738-1742 (e) Fürstner A., Grabowski J., Lehmann C.W. J. Org. Chem. 64:1999;8275-8280 (f) Fürstner A., Weintritt H. J. Am. Chem. Soc. 120:1998;2817-2825 (g) Fürstner A., Weintritt H., Hupperts A. J. Org. Chem. 60:1995;6637-6641 (h) Fürstner A., Hupperts A. J. Am. Chem. Soc. 117:1995;4468-4475.
    • (2002) Tetrahedron , vol.58 , pp. 6373-6380
    • Fürstner, A.1    Krause, H.2    Thiel, O.R.3
  • 9
    • 0034632402 scopus 로고    scopus 로고
    • For representative examples see: (a) Fürstner A., Leitner A. Angew. Chem., Int. Ed. 42:2003;308-311 (b) Fürstner A., Krause H., Thiel O.R. Tetrahedron. 58:2002;6373-6380 (c) Fürstner A., Gastner T. Org. Lett. 2:2000;2467-2470 (d) Fürstner A., Thiel O.R. J. Org. Chem. 65:2000;1738-1742 (e) Fürstner A., Grabowski J., Lehmann C.W. J. Org. Chem. 64:1999;8275-8280 (f) Fürstner A., Weintritt H. J. Am. Chem. Soc. 120:1998;2817-2825 (g) Fürstner A., Weintritt H., Hupperts A. J. Org. Chem. 60:1995;6637-6641 (h) Fürstner A., Hupperts A. J. Am. Chem. Soc. 117:1995;4468-4475.
    • (2000) Org. Lett. , vol.2 , pp. 2467-2470
    • Fürstner, A.1    Gastner, T.2
  • 10
    • 0038644039 scopus 로고    scopus 로고
    • For representative examples see: (a) Fürstner A., Leitner A. Angew. Chem., Int. Ed. 42:2003;308-311 (b) Fürstner A., Krause H., Thiel O.R. Tetrahedron. 58:2002;6373-6380 (c) Fürstner A., Gastner T. Org. Lett. 2:2000;2467-2470 (d) Fürstner A., Thiel O.R. J. Org. Chem. 65:2000;1738-1742 (e) Fürstner A., Grabowski J., Lehmann C.W. J. Org. Chem. 64:1999;8275-8280 (f) Fürstner A., Weintritt H. J. Am. Chem. Soc. 120:1998;2817-2825 (g) Fürstner A., Weintritt H., Hupperts A. J. Org. Chem. 60:1995;6637-6641 (h) Fürstner A., Hupperts A. J. Am. Chem. Soc. 117:1995;4468-4475.
    • (2000) J. Org. Chem. , vol.65 , pp. 1738-1742
    • Fürstner, A.1    Thiel, O.R.2
  • 11
    • 0038590297 scopus 로고    scopus 로고
    • For representative examples see: (a) Fürstner A., Leitner A. Angew. Chem., Int. Ed. 42:2003;308-311 (b) Fürstner A., Krause H., Thiel O.R. Tetrahedron. 58:2002;6373-6380 (c) Fürstner A., Gastner T. Org. Lett. 2:2000;2467-2470 (d) Fürstner A., Thiel O.R. J. Org. Chem. 65:2000;1738-1742 (e) Fürstner A., Grabowski J., Lehmann C.W. J. Org. Chem. 64:1999;8275-8280 (f) Fürstner A., Weintritt H. J. Am. Chem. Soc. 120:1998;2817-2825 (g) Fürstner A., Weintritt H., Hupperts A. J. Org. Chem. 60:1995;6637-6641 (h) Fürstner A., Hupperts A. J. Am. Chem. Soc. 117:1995;4468-4475.
    • (1999) J. Org. Chem. , vol.64 , pp. 8275-8280
    • Fürstner, A.1    Grabowski, J.2    Lehmann, C.W.3
  • 12
    • 0037644400 scopus 로고    scopus 로고
    • For representative examples see: (a) Fürstner A., Leitner A. Angew. Chem., Int. Ed. 42:2003;308-311 (b) Fürstner A., Krause H., Thiel O.R. Tetrahedron. 58:2002;6373-6380 (c) Fürstner A., Gastner T. Org. Lett. 2:2000;2467-2470 (d) Fürstner A., Thiel O.R. J. Org. Chem. 65:2000;1738-1742 (e) Fürstner A., Grabowski J., Lehmann C.W. J. Org. Chem. 64:1999;8275-8280 (f) Fürstner A., Weintritt H. J. Am. Chem. Soc. 120:1998;2817-2825 (g) Fürstner A., Weintritt H., Hupperts A. J. Org. Chem. 60:1995;6637-6641 (h) Fürstner A., Hupperts A. J. Am. Chem. Soc. 117:1995;4468-4475.
    • (1998) J. Am. Chem. Soc. , vol.120 , pp. 2817-2825
    • Fürstner, A.1    Weintritt, H.2
  • 13
    • 0028829479 scopus 로고
    • For representative examples see: (a) Fürstner A., Leitner A. Angew. Chem., Int. Ed. 42:2003;308-311 (b) Fürstner A., Krause H., Thiel O.R. Tetrahedron. 58:2002;6373-6380 (c) Fürstner A., Gastner T. Org. Lett. 2:2000;2467-2470 (d) Fürstner A., Thiel O.R. J. Org. Chem. 65:2000;1738-1742 (e) Fürstner A., Grabowski J., Lehmann C.W. J. Org. Chem. 64:1999;8275-8280 (f) Fürstner A., Weintritt H. J. Am. Chem. Soc. 120:1998;2817-2825 (g) Fürstner A., Weintritt H., Hupperts A. J. Org. Chem. 60:1995;6637-6641 (h) Fürstner A., Hupperts A. J. Am. Chem. Soc. 117:1995;4468-4475.
    • (1995) J. Org. Chem. , vol.60 , pp. 6637-6641
    • Fürstner, A.1    Weintritt, H.2    Hupperts, A.3
  • 14
    • 0000307431 scopus 로고
    • For representative examples see: (a) Fürstner A., Leitner A. Angew. Chem., Int. Ed. 42:2003;308-311 (b) Fürstner A., Krause H., Thiel O.R. Tetrahedron. 58:2002;6373-6380 (c) Fürstner A., Gastner T. Org. Lett. 2:2000;2467-2470 (d) Fürstner A., Thiel O.R. J. Org. Chem. 65:2000;1738-1742 (e) Fürstner A., Grabowski J., Lehmann C.W. J. Org. Chem. 64:1999;8275-8280 (f) Fürstner A., Weintritt H. J. Am. Chem. Soc. 120:1998;2817-2825 (g) Fürstner A., Weintritt H., Hupperts A. J. Org. Chem. 60:1995;6637-6641 (h) Fürstner A., Hupperts A. J. Am. Chem. Soc. 117:1995;4468-4475.
    • (1995) J. Am. Chem. Soc. , vol.117 , pp. 4468-4475
    • Fürstner, A.1    Hupperts, A.2
  • 18
    • 0042880263 scopus 로고    scopus 로고
    • For another synthesis of a pyrone embedded into a meta-cyclophane structure from our laboratory see:
    • For another synthesis of a pyrone embedded into a meta-cyclophane structure from our laboratory see: Fürstner A., Krause H. J. Org. Chem. 64:1999;8281-8286.
    • (1999) J. Org. Chem. , vol.64 , pp. 8281-8286
    • Fürstner, A.1    Krause, H.2
  • 19
    • 0034746687 scopus 로고    scopus 로고
    • For general reviews on metathesis see: (a) Trnka T.M., Grubbs R.H. Acc. Chem. Res. 34:2001;18-29 (b) Fürstner A. Angew. Chem., Int. Ed. 39:2000;3012-3043.
    • (2001) Acc. Chem. Res. , vol.34 , pp. 18-29
    • Trnka, T.M.1    Grubbs, R.H.2
  • 20
    • 0034746687 scopus 로고    scopus 로고
    • For general reviews on metathesis see: (a) Trnka T.M., Grubbs R.H. Acc. Chem. Res. 34:2001;18-29 (b) Fürstner A. Angew. Chem., Int. Ed. 39:2000;3012-3043.
    • (2000) Angew. Chem., Int. Ed. , vol.39 , pp. 3012-3043
    • Fürstner, A.1
  • 41
    • 0001803523 scopus 로고
    • The first indication of this striking chemoselectivity is found in an early publication of Schrock showing that tungsten alkylidyne complexes will metathezise 3-heptyne in the presence of admixed cis-2-pentene, cf.
    • The first indication of this striking chemoselectivity is found in an early publication of Schrock showing that tungsten alkylidyne complexes will metathezise 3-heptyne in the presence of admixed cis-2-pentene, cf.: Sancho J., Schrock R.R. J. Mol. Catal. 15:1982;75-79.
    • (1982) J. Mol. Catal. , vol.15 , pp. 75-79
    • Sancho, J.1    Schrock, R.R.2
  • 42
    • 0035905420 scopus 로고    scopus 로고
    • For more elaborate examples see the total syntheses of epothilone C, various prostaglandin derivatives, and the butenolide dehydrohomoancepsenolide: (a) Fürstner A., Mathes C., Lehmann C.W. Chem. Eur. J. 7:2001;5299-5317 (b) Fürstner A., Mathes C., Grela K. Chem. Commun. 2001;1057-1059 (c) Fürstner A., Grela K., Mathes C., Lehmann C.W. J. Am. Chem. Soc. 122:2000;11799-11805 (d) Fürstner A., Grela K. Angew. Chem., Int. Ed. 39:2000;1234-1236 (e) Fürstner A., Dierkes T. Org. Lett. 2:2000;2463-2465 (f) Fürstner A., Mathes C. Org. Lett. 3:2001;221-223.
    • (2001) Chem. Eur. J. , vol.7 , pp. 5299-5317
    • Fürstner, A.1    Mathes, C.2    Lehmann, C.W.3
  • 43
    • 0035927899 scopus 로고    scopus 로고
    • For more elaborate examples see the total syntheses of epothilone C, various prostaglandin derivatives, and the butenolide dehydrohomoancepsenolide: (a) Fürstner A., Mathes C., Lehmann C.W. Chem. Eur. J. 7:2001;5299-5317 (b) Fürstner A., Mathes C., Grela K. Chem. Commun. 2001;1057-1059 (c) Fürstner A., Grela K., Mathes C., Lehmann C.W. J. Am. Chem. Soc. 122:2000;11799-11805 (d) Fürstner A., Grela K. Angew. Chem., Int. Ed. 39:2000;1234-1236 (e) Fürstner A., Dierkes T. Org. Lett. 2:2000;2463-2465 (f) Fürstner A., Mathes C. Org. Lett. 3:2001;221-223.
    • (2001) Chem. Commun. , pp. 1057-1059
    • Fürstner, A.1    Mathes, C.2    Grela, K.3
  • 44
    • 0034614071 scopus 로고    scopus 로고
    • For more elaborate examples see the total syntheses of epothilone C, various prostaglandin derivatives, and the butenolide dehydrohomoancepsenolide: (a) Fürstner A., Mathes C., Lehmann C.W. Chem. Eur. J. 7:2001;5299-5317 (b) Fürstner A., Mathes C., Grela K. Chem. Commun. 2001;1057-1059 (c) Fürstner A., Grela K., Mathes C., Lehmann C.W. J. Am. Chem. Soc. 122:2000;11799-11805 (d) Fürstner A., Grela K. Angew. Chem., Int. Ed. 39:2000;1234-1236 (e) Fürstner A., Dierkes T. Org. Lett. 2:2000;2463-2465 (f) Fürstner A., Mathes C. Org. Lett. 3:2001;221-223.
    • (2000) J. Am. Chem. Soc. , vol.122 , pp. 11799-11805
    • Fürstner, A.1    Grela, K.2    Mathes, C.3    Lehmann, C.W.4
  • 45
    • 0038584256 scopus 로고    scopus 로고
    • For more elaborate examples see the total syntheses of epothilone C, various prostaglandin derivatives, and the butenolide dehydrohomoancepsenolide: (a) Fürstner A., Mathes C., Lehmann C.W. Chem. Eur. J. 7:2001;5299-5317 (b) Fürstner A., Mathes C., Grela K. Chem. Commun. 2001;1057-1059 (c) Fürstner A., Grela K., Mathes C., Lehmann C.W. J. Am. Chem. Soc. 122:2000;11799-11805 (d) Fürstner A., Grela K. Angew. Chem., Int. Ed. 39:2000;1234-1236 (e) Fürstner A., Dierkes T. Org. Lett. 2:2000;2463-2465 (f) Fürstner A., Mathes C. Org. Lett. 3:2001;221-223.
    • (2000) Angew. Chem., Int. Ed. , vol.39 , pp. 1234-1236
    • Fürstner, A.1    Grela, K.2
  • 46
    • 0034632359 scopus 로고    scopus 로고
    • For more elaborate examples see the total syntheses of epothilone C, various prostaglandin derivatives, and the butenolide dehydrohomoancepsenolide: (a) Fürstner A., Mathes C., Lehmann C.W. Chem. Eur. J. 7:2001;5299-5317 (b) Fürstner A., Mathes C., Grela K. Chem. Commun. 2001;1057-1059 (c) Fürstner A., Grela K., Mathes C., Lehmann C.W. J. Am. Chem. Soc. 122:2000;11799-11805 (d) Fürstner A., Grela K. Angew. Chem., Int. Ed. 39:2000;1234-1236 (e) Fürstner A., Dierkes T. Org. Lett. 2:2000;2463-2465 (f) Fürstner A., Mathes C. Org. Lett. 3:2001;221-223.
    • (2000) Org. Lett. , vol.2 , pp. 2463-2465
    • Fürstner, A.1    Dierkes, T.2
  • 47
    • 0000406859 scopus 로고    scopus 로고
    • For more elaborate examples see the total syntheses of epothilone C, various prostaglandin derivatives, and the butenolide dehydrohomoancepsenolide: (a) Fürstner A., Mathes C., Lehmann C.W. Chem. Eur. J. 7:2001;5299-5317 (b) Fürstner A., Mathes C., Grela K. Chem. Commun. 2001;1057-1059 (c) Fürstner A., Grela K., Mathes C., Lehmann C.W. J. Am. Chem. Soc. 122:2000;11799-11805 (d) Fürstner A., Grela K. Angew. Chem., Int. Ed. 39:2000;1234-1236 (e) Fürstner A., Dierkes T. Org. Lett. 2:2000;2463-2465 (f) Fürstner A., Mathes C. Org. Lett. 3:2001;221-223.
    • (2001) Org. Lett. , vol.3 , pp. 221-223
    • Fürstner, A.1    Mathes, C.2
  • 51
    • 0037162657 scopus 로고    scopus 로고
    • For leading applications see: (a) Hagiwara H., Kobayashi K., Miya S., Hoshi T., Suzuki T., Ando M., Okamoto T., Kobayashi M., Yamamoto I., Ohtsubo S., Kato M., Uda H. J. Org. Chem. 67:2002;5969-5976 (b) Oikawa H., Kobayashi T., Katayama K., Suzuki Y., Ichihara A. J. Org. Chem. 63:1998;8748-8756 (c) Smith A.B., Kinsho T., Sunazuka T., Omura S. Tetrahedron Lett. 37:1996;6461-6464 (d) Fehr M.J., Consiglio G., Scalone M., Schmid R. J. Org. Chem. 64:1999;5768-5776 (e) Ishibashi Y., Ohba S., Nishiyama S., Yamamura S. Tetrahedron Lett. 37:1996;2997-3000 (f) Cervello J., Marquet J., Moreno-Mañas M. Tetrahedron. 46:1990;2035-2046 (g) Cervello J., Marquet J., Moreno-Mañas M. J. Chem. Soc., Chem. Commun. 1987;644-645 (h) Oppolzer W., Moretti R., Bernardinelli G. Tetrahedron Lett. 27:1986;4713-4716. and literature cited therin.
    • (2002) J. Org. Chem. , vol.67 , pp. 5969-5976
    • Hagiwara, H.1    Kobayashi, K.2    Miya, S.3    Hoshi, T.4    Suzuki, T.5    Ando, M.6    Okamoto, T.7    Kobayashi, M.8    Yamamoto, I.9    Ohtsubo, S.10    Kato, M.11    Uda, H.12
  • 52
    • 0031765407 scopus 로고    scopus 로고
    • For leading applications see: (a) Hagiwara H., Kobayashi K., Miya S., Hoshi T., Suzuki T., Ando M., Okamoto T., Kobayashi M., Yamamoto I., Ohtsubo S., Kato M., Uda H. J. Org. Chem. 67:2002;5969-5976 (b) Oikawa H., Kobayashi T., Katayama K., Suzuki Y., Ichihara A. J. Org. Chem. 63:1998;8748-8756 (c) Smith A.B., Kinsho T., Sunazuka T., Omura S. Tetrahedron Lett. 37:1996;6461-6464 (d) Fehr M.J., Consiglio G., Scalone M., Schmid R. J. Org. Chem. 64:1999;5768-5776 (e) Ishibashi Y., Ohba S., Nishiyama S., Yamamura S. Tetrahedron Lett. 37:1996;2997-3000 (f) Cervello J., Marquet J., Moreno-Mañas M. Tetrahedron. 46:1990;2035-2046 (g) Cervello J., Marquet J., Moreno-Mañas M. J. Chem. Soc., Chem. Commun. 1987;644-645 (h) Oppolzer W., Moretti R., Bernardinelli G. Tetrahedron Lett. 27:1986;4713-4716. and literature cited therin.
    • (1998) J. Org. Chem. , vol.63 , pp. 8748-8756
    • Oikawa, H.1    Kobayashi, T.2    Katayama, K.3    Suzuki, Y.4    Ichihara, A.5
  • 53
    • 0030565604 scopus 로고    scopus 로고
    • For leading applications see: (a) Hagiwara H., Kobayashi K., Miya S., Hoshi T., Suzuki T., Ando M., Okamoto T., Kobayashi M., Yamamoto I., Ohtsubo S., Kato M., Uda H. J. Org. Chem. 67:2002;5969-5976 (b) Oikawa H., Kobayashi T., Katayama K., Suzuki Y., Ichihara A. J. Org. Chem. 63:1998;8748-8756 (c) Smith A.B., Kinsho T., Sunazuka T., Omura S. Tetrahedron Lett. 37:1996;6461-6464 (d) Fehr M.J., Consiglio G., Scalone M., Schmid R. J. Org. Chem. 64:1999;5768-5776 (e) Ishibashi Y., Ohba S., Nishiyama S., Yamamura S. Tetrahedron Lett. 37:1996;2997-3000 (f) Cervello J., Marquet J., Moreno-Mañas M. Tetrahedron. 46:1990;2035-2046 (g) Cervello J., Marquet J., Moreno-Mañas M. J. Chem. Soc., Chem. Commun. 1987;644-645 (h) Oppolzer W., Moretti R., Bernardinelli G. Tetrahedron Lett. 27:1986;4713-4716. and literature cited therin.
    • (1996) Tetrahedron Lett. , vol.37 , pp. 6461-6464
    • Smith, A.B.1    Kinsho, T.2    Sunazuka, T.3    Omura, S.4
  • 54
    • 0033529737 scopus 로고    scopus 로고
    • For leading applications see: (a) Hagiwara H., Kobayashi K., Miya S., Hoshi T., Suzuki T., Ando M., Okamoto T., Kobayashi M., Yamamoto I., Ohtsubo S., Kato M., Uda H. J. Org. Chem. 67:2002;5969-5976 (b) Oikawa H., Kobayashi T., Katayama K., Suzuki Y., Ichihara A. J. Org. Chem. 63:1998;8748-8756 (c) Smith A.B., Kinsho T., Sunazuka T., Omura S. Tetrahedron Lett. 37:1996;6461-6464 (d) Fehr M.J., Consiglio G., Scalone M., Schmid R. J. Org. Chem. 64:1999;5768-5776 (e) Ishibashi Y., Ohba S., Nishiyama S., Yamamura S. Tetrahedron Lett. 37:1996;2997-3000 (f) Cervello J., Marquet J., Moreno-Mañas M. Tetrahedron. 46:1990;2035-2046 (g) Cervello J., Marquet J., Moreno-Mañas M. J. Chem. Soc., Chem. Commun. 1987;644-645 (h) Oppolzer W., Moretti R., Bernardinelli G. Tetrahedron Lett. 27:1986;4713-4716. and literature cited therin.
    • (1999) J. Org. Chem. , vol.64 , pp. 5768-5776
    • Fehr, M.J.1    Consiglio, G.2    Scalone, M.3    Schmid, R.4
  • 55
    • 0029876114 scopus 로고    scopus 로고
    • For leading applications see: (a) Hagiwara H., Kobayashi K., Miya S., Hoshi T., Suzuki T., Ando M., Okamoto T., Kobayashi M., Yamamoto I., Ohtsubo S., Kato M., Uda H. J. Org. Chem. 67:2002;5969-5976 (b) Oikawa H., Kobayashi T., Katayama K., Suzuki Y., Ichihara A. J. Org. Chem. 63:1998;8748-8756 (c) Smith A.B., Kinsho T., Sunazuka T., Omura S. Tetrahedron Lett. 37:1996;6461-6464 (d) Fehr M.J., Consiglio G., Scalone M., Schmid R. J. Org. Chem. 64:1999;5768-5776 (e) Ishibashi Y., Ohba S., Nishiyama S., Yamamura S. Tetrahedron Lett. 37:1996;2997-3000 (f) Cervello J., Marquet J., Moreno-Mañas M. Tetrahedron. 46:1990;2035-2046 (g) Cervello J., Marquet J., Moreno-Mañas M. J. Chem. Soc., Chem. Commun. 1987;644-645 (h) Oppolzer W., Moretti R., Bernardinelli G. Tetrahedron Lett. 27:1986;4713-4716. and literature cited therin.
    • (1996) Tetrahedron Lett. , vol.37 , pp. 2997-3000
    • Ishibashi, Y.1    Ohba, S.2    Nishiyama, S.3    Yamamura, S.4
  • 56
    • 30444433269 scopus 로고
    • For leading applications see: (a) Hagiwara H., Kobayashi K., Miya S., Hoshi T., Suzuki T., Ando M., Okamoto T., Kobayashi M., Yamamoto I., Ohtsubo S., Kato M., Uda H. J. Org. Chem. 67:2002;5969-5976 (b) Oikawa H., Kobayashi T., Katayama K., Suzuki Y., Ichihara A. J. Org. Chem. 63:1998;8748-8756 (c) Smith A.B., Kinsho T., Sunazuka T., Omura S. Tetrahedron Lett. 37:1996;6461-6464 (d) Fehr M.J., Consiglio G., Scalone M., Schmid R. J. Org. Chem. 64:1999;5768-5776 (e) Ishibashi Y., Ohba S., Nishiyama S., Yamamura S. Tetrahedron Lett. 37:1996;2997-3000 (f) Cervello J., Marquet J., Moreno-Mañas M. Tetrahedron. 46:1990;2035-2046 (g) Cervello J., Marquet J., Moreno-Mañas M. J. Chem. Soc., Chem. Commun. 1987;644-645 (h) Oppolzer W., Moretti R., Bernardinelli G. Tetrahedron Lett. 27:1986;4713-4716. and literature cited therin.
    • (1990) Tetrahedron , vol.46 , pp. 2035-2046
    • Cervello, J.1    Marquet, J.2    Moreno-Mañas, M.3
  • 57
    • 37049074877 scopus 로고
    • For leading applications see: (a) Hagiwara H., Kobayashi K., Miya S., Hoshi T., Suzuki T., Ando M., Okamoto T., Kobayashi M., Yamamoto I., Ohtsubo S., Kato M., Uda H. J. Org. Chem. 67:2002;5969-5976 (b) Oikawa H., Kobayashi T., Katayama K., Suzuki Y., Ichihara A. J. Org. Chem. 63:1998;8748-8756 (c) Smith A.B., Kinsho T., Sunazuka T., Omura S. Tetrahedron Lett. 37:1996;6461-6464 (d) Fehr M.J., Consiglio G., Scalone M., Schmid R. J. Org. Chem. 64:1999;5768-5776 (e) Ishibashi Y., Ohba S., Nishiyama S., Yamamura S. Tetrahedron Lett. 37:1996;2997-3000 (f) Cervello J., Marquet J., Moreno-Mañas M. Tetrahedron. 46:1990;2035-2046 (g) Cervello J., Marquet J., Moreno-Mañas M. J. Chem. Soc., Chem. Commun. 1987;644-645 (h) Oppolzer W., Moretti R., Bernardinelli G. Tetrahedron Lett. 27:1986;4713-4716. and literature cited therin.
    • (1987) J. Chem. Soc., Chem. Commun. , pp. 644-645
    • Cervello, J.1    Marquet, J.2    Moreno-Mañas, M.3
  • 58
    • 0000369244 scopus 로고
    • For leading applications see: (a) Hagiwara H., Kobayashi K., Miya S., Hoshi T., Suzuki T., Ando M., Okamoto T., Kobayashi M., Yamamoto I., Ohtsubo S., Kato M., Uda H. J. Org. Chem. 67:2002;5969-5976 (b) Oikawa H., Kobayashi T., Katayama K., Suzuki Y., Ichihara A. J. Org. Chem. 63:1998;8748-8756 (c) Smith A.B., Kinsho T., Sunazuka T., Omura S. Tetrahedron Lett. 37:1996;6461-6464 (d) Fehr M.J., Consiglio G., Scalone M., Schmid R. J. Org. Chem. 64:1999;5768-5776 (e) Ishibashi Y., Ohba S., Nishiyama S., Yamamura S. Tetrahedron Lett. 37:1996;2997-3000 (f) Cervello J., Marquet J., Moreno-Mañas M. Tetrahedron. 46:1990;2035-2046 (g) Cervello J., Marquet J., Moreno-Mañas M. J. Chem. Soc., Chem. Commun. 1987;644-645 (h) Oppolzer W., Moretti R., Bernardinelli G. Tetrahedron Lett. 27:1986;4713-4716. and literature cited therin.
    • (1986) Tetrahedron Lett. , vol.27 , pp. 4713-4716
    • Oppolzer, W.1    Moretti, R.2    Bernardinelli, G.3
  • 59
    • 0028864552 scopus 로고
    • (a) Lygo B. Tetrahedron. 51:1995;12859-12868
    • (1995) Tetrahedron , vol.51 , pp. 12859-12868
    • Lygo, B.1


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.