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Volumn 15, Issue 1, 2004, Pages 81-89

Formal total synthesis of (-)-salicylihalamides A and B

Author keywords

[No Author keywords available]

Indexed keywords

AMIDE; EPOXIDE; SALICYLIHALAMIDE A; SALICYLIHALAMIDE B; UNCLASSIFIED DRUG;

EID: 0348048813     PISSN: 09574166     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.tetasy.2003.10.038     Document Type: Article
Times cited : (52)

References (31)
  • 2
    • 0034605899 scopus 로고    scopus 로고
    • Total syntheses: (a) Wu Y., Esser L., De Brabander J.K. Angew. Chem. 39(23):2000;4308 (b) Labrecque D., Charron S., Rej R., Blais C., Lamothe S. Tetrahedron Lett. 42:2001;2645 (c) Snider B.B., Song F. Org. Lett. 3:2001;1817 (d) Smith A.B., Zheng J. Synlett. 2001;1019 Furstner A., Dierkes T., Thiel O.R., Blanda G. Chem. Eur. J. 7(24):2001;5286 (f) Wu Y., Liao X., Wang R., Xie S.S., De Brabander J.K. J. Am. Chem. Soc. 124:2002;3245.
    • (2000) Angew. Chem. , vol.39 , Issue.23 , pp. 4308
    • Wu, Y.1    Esser, L.2    De Brabander, J.K.3
  • 3
    • 0035795049 scopus 로고    scopus 로고
    • Total syntheses: (a) Wu Y., Esser L., De Brabander J.K. Angew. Chem. 39(23):2000;4308 (b) Labrecque D., Charron S., Rej R., Blais C., Lamothe S. Tetrahedron Lett. 42:2001;2645 (c) Snider B.B., Song F. Org. Lett. 3:2001;1817 (d) Smith A.B., Zheng J. Synlett. 2001;1019 Furstner A., Dierkes T., Thiel O.R., Blanda G. Chem. Eur. J. 7(24):2001;5286 (f) Wu Y., Liao X., Wang R., Xie S.S., De Brabander J.K. J. Am. Chem. Soc. 124:2002;3245.
    • (2001) Tetrahedron Lett. , vol.42 , pp. 2645
    • Labrecque, D.1    Charron, S.2    Rej, R.3    Blais, C.4    Lamothe, S.5
  • 4
    • 0035859315 scopus 로고    scopus 로고
    • Total syntheses: (a) Wu Y., Esser L., De Brabander J.K. Angew. Chem. 39(23):2000;4308 (b) Labrecque D., Charron S., Rej R., Blais C., Lamothe S. Tetrahedron Lett. 42:2001;2645 (c) Snider B.B., Song F. Org. Lett. 3:2001;1817 (d) Smith A.B., Zheng J. Synlett. 2001;1019 Furstner A., Dierkes T., Thiel O.R., Blanda G. Chem. Eur. J. 7(24):2001;5286 (f) Wu Y., Liao X., Wang R., Xie S.S., De Brabander J.K. J. Am. Chem. Soc. 124:2002;3245.
    • (2001) Org. Lett. , vol.3 , pp. 1817
    • Snider, B.B.1    Song, F.2
  • 5
    • 0034966895 scopus 로고    scopus 로고
    • Total syntheses: (a) Wu Y., Esser L., De Brabander J.K. Angew. Chem. 39(23):2000;4308 (b) Labrecque D., Charron S., Rej R., Blais C., Lamothe S. Tetrahedron Lett. 42:2001;2645 (c) Snider B.B., Song F. Org. Lett. 3:2001;1817 (d) Smith A.B., Zheng J. Synlett. 2001;1019 Furstner A., Dierkes T., Thiel O.R., Blanda G. Chem. Eur. J. 7(24):2001;5286 (f) Wu Y., Liao X., Wang R., Xie S.S., De Brabander J.K. J. Am. Chem. Soc. 124:2002;3245.
    • (2001) Synlett , pp. 1019
    • Smith, A.B.1    Zheng, J.2
  • 6
    • 0035905656 scopus 로고    scopus 로고
    • Total syntheses: (a) Wu Y., Esser L., De Brabander J.K. Angew. Chem. 39(23):2000;4308 (b) Labrecque D., Charron S., Rej R., Blais C., Lamothe S. Tetrahedron Lett. 42:2001;2645 (c) Snider B.B., Song F. Org. Lett. 3:2001;1817 (d) Smith A.B., Zheng J. Synlett. 2001;1019 Furstner A., Dierkes T., Thiel O.R., Blanda G. Chem. Eur. J. 7(24):2001;5286 (f) Wu Y., Liao X., Wang R., Xie S.S., De Brabander J.K. J. Am. Chem. Soc. 124:2002;3245.
    • (2001) Chem. Eur. J. , vol.7 , Issue.24 , pp. 5286
    • Furstner, A.1    Dierkes, T.2    Thiel, O.R.3    Blanda, G.4
  • 7
    • 0037012401 scopus 로고    scopus 로고
    • Total syntheses: (a) Wu Y., Esser L., De Brabander J.K. Angew. Chem. 39(23):2000;4308 (b) Labrecque D., Charron S., Rej R., Blais C., Lamothe S. Tetrahedron Lett. 42:2001;2645 (c) Snider B.B., Song F. Org. Lett. 3:2001;1817 (d) Smith A.B., Zheng J. Synlett. 2001;1019 Furstner A., Dierkes T., Thiel O.R., Blanda G. Chem. Eur. J. 7(24):2001;5286 (f) Wu Y., Liao X., Wang R., Xie S.S., De Brabander J.K. J. Am. Chem. Soc. 124:2002;3245.
    • (2002) J. Am. Chem. Soc. , vol.124 , pp. 3245
    • Wu, Y.1    Liao, X.2    Wang, R.3    Xie, S.S.4    De Brabander, J.K.5
  • 8
    • 0035819597 scopus 로고    scopus 로고
    • Partial syntheses and model studies: (a) George G.I., Ahn Y.M., Blackman B., Farokhi F., Flaherty P.T., Mossman C.J., Roy S., Yang K.L. Chem. Commun. 2001;255 (b) Wu Y., Seguil O.R., De Brabander J.K. Org. Lett. 2:2000;4241 (c) Bhattacharjee A., De Brabander J.K. Tetrahedron Lett. 41:2000;8069 (d) Feutrill J.T., Holloway G.A., Hilli F., Hugel H.M., Rizzacasa M.A. Tetrahedron Lett. 41:2000;8569 (e) Furstner A., Oliver R., Blanda G. Org. Lett. 2:2000;3731 (f) Scheufler F., Maier M.E. Synlett. 2001;1221 (g) Bauer M., Maier M.E. Org. Lett. 4:2002;2205.
    • (2001) Chem. Commun. , pp. 255
    • George, G.I.1    Ahn, Y.M.2    Blackman, B.3    Farokhi, F.4    Flaherty, P.T.5    Mossman, C.J.6    Roy, S.7    Yang, K.L.8
  • 9
    • 0034727948 scopus 로고    scopus 로고
    • Partial syntheses and model studies: (a) George G.I., Ahn Y.M., Blackman B., Farokhi F., Flaherty P.T., Mossman C.J., Roy S., Yang K.L. Chem. Commun. 2001;255 (b) Wu Y., Seguil O.R., De Brabander J.K. Org. Lett. 2:2000;4241 (c) Bhattacharjee A., De Brabander J.K. Tetrahedron Lett. 41:2000;8069 (d) Feutrill J.T., Holloway G.A., Hilli F., Hugel H.M., Rizzacasa M.A. Tetrahedron Lett. 41:2000;8569 (e) Furstner A., Oliver R., Blanda G. Org. Lett. 2:2000;3731 (f) Scheufler F., Maier M.E. Synlett. 2001;1221 (g) Bauer M., Maier M.E. Org. Lett. 4:2002;2205.
    • (2000) Org. Lett. , vol.2 , pp. 4241
    • Wu, Y.1    Seguil, O.R.2    De Brabander, J.K.3
  • 10
    • 0034649130 scopus 로고    scopus 로고
    • Partial syntheses and model studies: (a) George G.I., Ahn Y.M., Blackman B., Farokhi F., Flaherty P.T., Mossman C.J., Roy S., Yang K.L. Chem. Commun. 2001;255 (b) Wu Y., Seguil O.R., De Brabander J.K. Org. Lett. 2:2000;4241 (c) Bhattacharjee A., De Brabander J.K. Tetrahedron Lett. 41:2000;8069 (d) Feutrill J.T., Holloway G.A., Hilli F., Hugel H.M., Rizzacasa M.A. Tetrahedron Lett. 41:2000;8569 (e) Furstner A., Oliver R., Blanda G. Org. Lett. 2:2000;3731 (f) Scheufler F., Maier M.E. Synlett. 2001;1221 (g) Bauer M., Maier M.E. Org. Lett. 4:2002;2205.
    • (2000) Tetrahedron Lett. , vol.41 , pp. 8069
    • Bhattacharjee, A.1    De Brabander, J.K.2
  • 11
    • 0034727314 scopus 로고    scopus 로고
    • Partial syntheses and model studies: (a) George G.I., Ahn Y.M., Blackman B., Farokhi F., Flaherty P.T., Mossman C.J., Roy S., Yang K.L. Chem. Commun. 2001;255 (b) Wu Y., Seguil O.R., De Brabander J.K. Org. Lett. 2:2000;4241 (c) Bhattacharjee A., De Brabander J.K. Tetrahedron Lett. 41:2000;8069 (d) Feutrill J.T., Holloway G.A., Hilli F., Hugel H.M., Rizzacasa M.A. Tetrahedron Lett. 41:2000;8569 (e) Furstner A., Oliver R., Blanda G. Org. Lett. 2:2000;3731 (f) Scheufler F., Maier M.E. Synlett. 2001;1221 (g) Bauer M., Maier M.E. Org. Lett. 4:2002;2205.
    • (2000) Tetrahedron Lett. , vol.41 , pp. 8569
    • Feutrill, J.T.1    Holloway, G.A.2    Hilli, F.3    Hugel, H.M.4    Rizzacasa, M.A.5
  • 12
    • 0034676533 scopus 로고    scopus 로고
    • Partial syntheses and model studies: (a) George G.I., Ahn Y.M., Blackman B., Farokhi F., Flaherty P.T., Mossman C.J., Roy S., Yang K.L. Chem. Commun. 2001;255 (b) Wu Y., Seguil O.R., De Brabander J.K. Org. Lett. 2:2000;4241 (c) Bhattacharjee A., De Brabander J.K. Tetrahedron Lett. 41:2000;8069 (d) Feutrill J.T., Holloway G.A., Hilli F., Hugel H.M., Rizzacasa M.A. Tetrahedron Lett. 41:2000;8569 (e) Furstner A., Oliver R., Blanda G. Org. Lett. 2:2000;3731 (f) Scheufler F., Maier M.E. Synlett. 2001;1221 (g) Bauer M., Maier M.E. Org. Lett. 4:2002;2205.
    • (2000) Org. Lett. , vol.2 , pp. 3731
    • Furstner, A.1    Oliver, R.2    Blanda, G.3
  • 13
    • 0034910864 scopus 로고    scopus 로고
    • Partial syntheses and model studies: (a) George G.I., Ahn Y.M., Blackman B., Farokhi F., Flaherty P.T., Mossman C.J., Roy S., Yang K.L. Chem. Commun. 2001;255 (b) Wu Y., Seguil O.R., De Brabander J.K. Org. Lett. 2:2000;4241 (c) Bhattacharjee A., De Brabander J.K. Tetrahedron Lett. 41:2000;8069 (d) Feutrill J.T., Holloway G.A., Hilli F., Hugel H.M., Rizzacasa M.A. Tetrahedron Lett. 41:2000;8569 (e) Furstner A., Oliver R., Blanda G. Org. Lett. 2:2000;3731 (f) Scheufler F., Maier M.E. Synlett. 2001;1221 (g) Bauer M., Maier M.E. Org. Lett. 4:2002;2205.
    • (2001) Synlett , pp. 1221
    • Scheufler, F.1    Maier, M.E.2
  • 14
    • 0037182735 scopus 로고    scopus 로고
    • Partial syntheses and model studies: (a) George G.I., Ahn Y.M., Blackman B., Farokhi F., Flaherty P.T., Mossman C.J., Roy S., Yang K.L. Chem. Commun. 2001;255 (b) Wu Y., Seguil O.R., De Brabander J.K. Org. Lett. 2:2000;4241 (c) Bhattacharjee A., De Brabander J.K. Tetrahedron Lett. 41:2000;8069 (d) Feutrill J.T., Holloway G.A., Hilli F., Hugel H.M., Rizzacasa M.A. Tetrahedron Lett. 41:2000;8569 (e) Furstner A., Oliver R., Blanda G. Org. Lett. 2:2000;3731 (f) Scheufler F., Maier M.E. Synlett. 2001;1221 (g) Bauer M., Maier M.E. Org. Lett. 4:2002;2205.
    • (2002) Org. Lett. , vol.4 , pp. 2205
    • Bauer, M.1    Maier, M.E.2
  • 20
    • 0035898772 scopus 로고    scopus 로고
    • Similar alcohol with opposite center at C3 position was prepared earlier by our group using (S) epoxide as given in
    • Similar alcohol with opposite center at C3 position was prepared earlier by our group using (S) epoxide as given in Yadav J.S., Bandyopadhyay A., Kunwar A.C. Tetrahedron Lett. 42:2001;4907.
    • (2001) Tetrahedron Lett. , vol.42 , pp. 4907
    • Yadav, J.S.1    Bandyopadhyay, A.2    Kunwar, A.C.3
  • 26
    • 85030920616 scopus 로고
    • The compound was prepared from anisole as given in Vogel's Text Book of Practical Organic Chemistry. p 1117
    • The compound was prepared from anisole as given in Vogel's Text Book of Practical Organic Chemistry. 5th ed. 1989;. p 1117.
    • (1989) 5th Ed.


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