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Volumn 47, Issue 38, 2008, Pages 7182-7225

The continuing saga of the marine polyether biotoxins

Author keywords

Biotoxins; Maitotoxin; Natural products; Polyethers; Total synthesis

Indexed keywords

BIOCHEMISTRY; ETHERS; MECHANISMS; ORGANIC COMPOUNDS; POLYETHERS; POLYMERS; RAW MATERIALS; SODIUM;

EID: 53249152133     PISSN: 14337851     EISSN: None     Source Type: Journal    
DOI: 10.1002/anie.200801696     Document Type: Review
Times cited : (171)

References (283)
  • 2
    • 84889385554 scopus 로고    scopus 로고
    • Phycotoxins: Chemistry and Biochemistry (Ed.: L. M. Botana); Blackwell Publishing, Ames, 2007, p. 345.
    • b) Phycotoxins: Chemistry and Biochemistry (Ed.: L. M. Botana); Blackwell Publishing, Ames, 2007, p. 345.
  • 12
  • 43
    • 53249091711 scopus 로고    scopus 로고
    • The following distances [A] were obtained from the crystal structure of brevetoxin B: A-C 4.832, B-D 4.722, C-E 5.651, D-F 5.876, E-G 4.821, F-H 4.816, G-I 6.052, H-J 4.777, I-K 4.796.
    • The following distances [A] were obtained from the crystal structure of brevetoxin B: A-C 4.832, B-D 4.722, C-E 5.651, D-F 5.876, E-G 4.821, F-H 4.816, G-I 6.052, H-J 4.777, I-K 4.796.
  • 47
    • 0000563379 scopus 로고
    • For previous reviews on the chemistry and synthesis of polyether natural products, see: a
    • For previous reviews on the chemistry and synthesis of polyether natural products, see: a) E. Alvarez, M.-L. Candenas, R. Perez, J. L. Ravelo, J. D. Martin, Chem. Rev. 1995, 95, 1953;
    • (1995) Chem. Rev , vol.95 , pp. 1953
    • Alvarez, E.1    Candenas, M.-L.2    Perez, R.3    Ravelo, J.L.4    Martin, J.D.5
  • 50
    • 30744459350 scopus 로고    scopus 로고
    • d) T. Nakata, Chem. Rev. 2005, 105, 4314;
    • (2005) Chem. Rev , vol.105 , pp. 4314
    • Nakata, T.1
  • 51
    • 30744476469 scopus 로고    scopus 로고
    • e) M. Inoue, Chem. Rev. 2005, 105, 4379;
    • (2005) Chem. Rev , vol.105 , pp. 4379
    • Inoue, M.1
  • 57
    • 53249105134 scopus 로고    scopus 로고
    • Recently Gallimore and Spencer have expanded on Nakanishi Is biosynthetic hypothesis: A. R. Gallimore, J. B. Spencer, Angew. Chem. 2006, 118, 4514;
    • Recently Gallimore and Spencer have expanded on Nakanishi Is biosynthetic hypothesis: A. R. Gallimore, J. B. Spencer, Angew. Chem. 2006, 118, 4514;
  • 59
    • 53249105135 scopus 로고
    • NIH application GM31398-01 submission date: February 24
    • a) NIH application GM31398-01 (submission date: February 24, 1982);
    • (1982)
  • 66
    • 0012815040 scopus 로고    scopus 로고
    • Substrates are easily accessed through a Sharpless asymmetric epoxidation: a T. Katsuki, K. B. Sharpless, J. Am. Chem. Soc. 1980, 102, 5974;
    • Substrates are easily accessed through a Sharpless asymmetric epoxidation: a) T. Katsuki, K. B. Sharpless, J. Am. Chem. Soc. 1980, 102, 5974;
  • 99
    • 22744453115 scopus 로고    scopus 로고
    • for a review of olefin metathesis, see: c
    • for a review of olefin metathesis, see: c) K. C. Nicolaou, P. G. Bulger, D. Sarlah, Angew. Chem. 2005, 117, 4564;
    • (2005) Angew. Chem , vol.117 , pp. 4564
    • Nicolaou, K.C.1    Bulger, P.G.2    Sarlah, D.3
  • 101
    • 33747612878 scopus 로고    scopus 로고
    • For a review summarizing the applications of olefin metathesis in the synthesis of fused polyethers, see: J. S. Clark, Chem. Commun. 2006, 3571
    • For a review summarizing the applications of olefin metathesis in the synthesis of fused polyethers, see: J. S. Clark, Chem. Commun. 2006, 3571.
  • 126
    • 53249122670 scopus 로고    scopus 로고
    • for a review on the Suzuki reaction with alkyl boron species, see: b S. R. Chemler, D. Trauner, S. J. Danishefsky, Angew. Chem. 2001, 113, 4676;
    • for a review on the Suzuki reaction with alkyl boron species, see: b) S. R. Chemler, D. Trauner, S. J. Danishefsky, Angew. Chem. 2001, 113, 4676;
  • 129
    • 0032580462 scopus 로고    scopus 로고
    • for an earlier study from the same group on the use of Se,O-acetals for the same reaction, see: M. Sasaki, M. Inoue, T. Noguchi, A. Takeichi, K. Tachibana, Tetrahedron Lett. 1998, 39, 2783.
    • for an earlier study from the same group on the use of Se,O-acetals for the same reaction, see: M. Sasaki, M. Inoue, T. Noguchi, A. Takeichi, K. Tachibana, Tetrahedron Lett. 1998, 39, 2783.
  • 134
    • 2142715741 scopus 로고    scopus 로고
    • 2-promoted reactions, see: a G. A. Molander, C. R. Harris, Chem. Rev. 1996, 96, 307;
    • 2-promoted reactions, see: a) G. A. Molander, C. R. Harris, Chem. Rev. 1996, 96, 307;
  • 186
    • 0028880055 scopus 로고    scopus 로고
    • K. C. Nicolaou, C.-K. Hwang, M. E. Duggan, D. A. Nugiel, Y. Abe, K. BalReddy, ## S. A. DeFrees, D. R. Reddy, R. A. Awartani, S. R. Conley, F. P. J. T. Rutjes, E. A. Theodorakis, J. Am. Chem. Soc. 1995, 117, 10227;
    • h) K. C. Nicolaou, C.-K. Hwang, M. E. Duggan, D. A. Nugiel, Y. Abe, K. BalReddy, ## S. A. DeFrees, D. R. Reddy, R. A. Awartani, S. R. Conley, F. P. J. T. Rutjes, E. A. Theodorakis, J. Am. Chem. Soc. 1995, 117, 10227;
  • 193
    • 53249134247 scopus 로고    scopus 로고
    • G. D. Van Duyne in Marine Toxins: Origin, Structure, and Molecular Pharmacology (Eds: S. Hall, G. Strichartz), American Chemical Society, Washington, DC, 1990, pp. 144-160.
    • G. D. Van Duyne in Marine Toxins: Origin, Structure, and Molecular Pharmacology (Eds: S. Hall, G. Strichartz), American Chemical Society, Washington, DC, 1990, pp. 144-160.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.