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Volumn 76, Issue 11, 2011, Pages 4221-4259

Natural products synthesis: Enabling tools to penetrate nature's secrets of bioqenesis and biomechanism

Author keywords

[No Author keywords available]

Indexed keywords

CHEMICAL SYNTHESIS; COMPLEX MOLECULES; ENABLING TOOLS; NATURAL PRODUCTS; NATURALLY OCCURRING; SECONDARY METABOLITES; SELECTED EXAMPLES; SYNTHETIC TECHNOLOGY; TOTAL SYNTHESIS;

EID: 79958763837     PISSN: 00223263     EISSN: 15206904     Source Type: Journal    
DOI: 10.1021/Jo2003693     Document Type: Review
Times cited : (26)

References (392)
  • 26
    • 0000250093 scopus 로고
    • For reviews on the chemistry of bicyclomycin, see: (a) Williams, R M.; Durham, C. A Chem. Rev. 1988, 88, 511-540.
    • (1988) Chem. Rev. , vol.88 , pp. 511-540
    • Williams, R.M.1    Durham, C.A.2
  • 27
    • 79958749254 scopus 로고
    • Stereoselective synthetic and mechanistic chemistry of bicyclomycin
    • Atta-ur-Rahman, Ed.; Elsevier: Amsterdam
    • (b) Williams, R. M. Stereoselective Synthetic and Mechanistic Chemistry of Bicyclomycin. In Studies in Natural Products Chemistry; Atta-ur-Rahman, Ed.; Elsevier: Amsterdam, 1993; Vol. 12.
    • (1993) Studies in Natural Products Chemistry , vol.12
    • Williams, R.M.1
  • 85
    • 79958718179 scopus 로고    scopus 로고
    • Finefield, J. M.; Greshock, T. J.; Sherman, D. H.; Tsukamoto, S.; Williams, R. M. Unpublished results
    • Finefield, J. M.; Greshock, T. J.; Sherman, D. H.; Tsukamoto, S.; Williams, R. M. Unpublished results.
  • 90
    • 79958693694 scopus 로고    scopus 로고
    • Phil Baran and co-workers were the first to corroborate the absolute configuration of the (+)-stephacidin Aproduced by Aspergillus ochraceus through their elegant total synthesis of both antipodes; see ref 27
    • Phil Baran and co-workers were the first to corroborate the absolute configuration of the (+)-stephacidin Aproduced by Aspergillus ochraceus through their elegant total synthesis of both antipodes; see ref 27.
  • 97
    • 0030729616 scopus 로고    scopus 로고
    • Errata
    • J. Am. Chem. Soc. 1997, 119, 9588 (Errata)
    • (1997) J. Am. Chem. Soc. , vol.119 , pp. 9588
  • 101
    • 79958741339 scopus 로고    scopus 로고
    • Ph.D. Thesis, ETH
    • Arigoni and Kellenberger studied the biosynthesis of β-methylproline in bottromycin and found this to be derived from S-proline and S-adenosyl methionine; see: Kellenberger, J. L. Ph.D. Thesis, ETH, 1997.
    • (1997)
    • Kellenberger, J.L.1
  • 107
    • 0000644470 scopus 로고    scopus 로고
    • Biosynthesis of prenylated alkaloids derived from tryptophan
    • Leeper, F., Vederas, J. C., Eds.; Springer-Verlag: Berlin
    • For some reviews on the synthesis and biosynthesis of the prenylated indole alkaloids, see: (a) Williams, R. M.; Sanz-Cervera, J. F.; Stocking, E. Biosynthesis of Prenylated Alkaloids Derived from Tryptophan. In Topics in Current Chemistry, Volume on Biosynthesis - Terpenes and Alkaloids; Leeper, F., Vederas, J. C., Eds.; Springer-Verlag: Berlin, 2000; Vol. 209, pp 97-173.
    • (2000) Topics in Current Chemistry, Volume on Biosynthesis - Terpenes and Alkaloids , vol.209 , pp. 97-173
    • Williams, R.M.1    Sanz-Cervera, J.F.2    Stocking, E.3
  • 111
    • 84885511949 scopus 로고    scopus 로고
    • Biomimetic synthesis of alkaloids derived from tryptophan: Dioxopiperazine alkaloids
    • Poupon, E., Nay, B., Eds.; Wiley-VCH: Weinheim, in press
    • (e) Welch., T.; Williams, R. M. Biomimetic Synthesis of Alkaloids Derived from Tryptophan: Dioxopiperazine Alkaloids. In Biomimetic Organic Synthesis; Poupon, E., Nay, B., Eds.; Wiley-VCH: Weinheim, 2011; in press,
    • (2011) Biomimetic Organic Synthesis
    • Williams, R.M.1
  • 123
    • 0029937757 scopus 로고    scopus 로고
    • Sharpless-based methodology has been applied to the synthesis of these amino alcohols; see: Chang, H.-T.; Sharpless, K. B. Tetrahedron Lett. 1996, 37, 3219-3222.
    • (1996) Tetrahedron Lett. , vol.37 , pp. 3219-3222
    • Chang, H.-T.1    Sharpless, K.B.2
  • 128
    • 0002618911 scopus 로고
    • Hassner, A., Ed.; JAI Press: Greenwich
    • (c) Williams, R. M. Advances in Asymmetric Synthesis; Hassner, A., Ed.; JAI Press: Greenwich, 1995; Vol. 1, pp 45-94.
    • (1995) Advances in Asymmetric Synthesis , vol.1 , pp. 45-94
    • Williams, R.M.1
  • 192
    • 34547178270 scopus 로고    scopus 로고
    • For a review, see
    • (i) Trost, B. M.; Stiles, D. T. Org. Lett. 2007, 9, 2763-2766. For a review, see:
    • (2007) Org. Lett. , vol.9 , pp. 2763-2766
    • Trost, B.M.1    Stiles, D.T.2
  • 194
    • 79958703344 scopus 로고    scopus 로고
    • Ph.D. dissertation, Colorado State University
    • See ref 62; see also: Sebahar, P. Ph.D. dissertation, Colorado State University, 2003.
    • (2003)
    • Sebahar, P.1
  • 200
    • 79958718920 scopus 로고    scopus 로고
    • For synthetic approaches to palau'amine and congeners, see references cited in ref 92a
    • For synthetic approaches to palau'amine and congeners, see references cited in ref 92a.
  • 226
    • 79958752254 scopus 로고    scopus 로고
    • Paclitaxel, the generic name for Taxol, is a registered trademark of Bristol-Myers Squibb. Because of the greater familiarity with the word Taxol, this will be used throughout this article, and the trademark symbol has been deleted for the sake of clarity and brevity. For reviews, see
    • Paclitaxel, the generic name for Taxol, is a registered trademark of Bristol-Myers Squibb. Because of the greater familiarity with the word Taxol, this will be used throughout this article, and the trademark symbol has been deleted for the sake of clarity and brevity. For reviews, see:
  • 233
    • 0002553350 scopus 로고
    • Biosynthesis of taxol
    • Suffness, M., Ed.; CRC Press: Boca Raton, FL
    • (g) Floss, H. G.; Mocek, U. Biosynthesis of Taxol. In Taxol: Science and Applications; Suffness, M., Ed.; CRC Press: Boca Raton, FL, 1995.
    • (1995) Taxol: Science and Applications
    • Floss, H.G.1    Mocek, U.2
  • 244
    • 0028353983 scopus 로고
    • (i) J. Am. Chem. Soc. 1994, 116, 1599-1600.
    • (1994) J. Am. Chem. Soc. , vol.116 , pp. 1599-1600
  • 257
    • 79958748501 scopus 로고
    • Bioactive metabolites of the endophytic fungi of pacific yew
    • American Chemical Society: Washington, DC, Chapter 6
    • (f) Stierle, A.; Stierle, D.; Strobel, G.; Bignami, G.; Grothaus, P. Bioactive Metabolites of the Endophytic Fungi of Pacific Yew, Taxus brevifolia. Taxane Anticancer Agents; American Chemical Society: Washington, DC, 1995; Chapter 6, pp 82-97.
    • (1995) Taxus Brevifolia. Taxane Anticancer Agents , pp. 82-97
    • Stierle, A.1    Stierle, D.2    Strobel, G.3    Bignami, G.4    Grothaus, P.5
  • 272
    • 79958759479 scopus 로고    scopus 로고
    • Ph.D. dissertation, Elucidating the Biosynthetic Pathway to Taxol, Colorado State University
    • (b) Rubenstein, S. M. Ph.D. dissertation, Elucidating the Biosynthetic Pathway to Taxol, Colorado State University, 1996.
    • (1996)
    • Rubenstein, S.M.1
  • 275
    • 0141583800 scopus 로고    scopus 로고
    • Researchers probe steps of taxol biosynthesis
    • (b) Borman, S. Researchers Probe Steps of Taxol Biosynthesis. Chem. Eng. News 1996, No. July 1, 27-29.
    • (1996) Chem. Eng. News , Issue.JULY 1 , pp. 27-29
    • Borman, S.1
  • 291
    • 79958754112 scopus 로고    scopus 로고
    • Unpublished results
    • Croteau, R. Unpublished results.
    • Croteau, R.1
  • 316
    • 0001676690 scopus 로고    scopus 로고
    • (a) For a comprehensive review on DNA cross-linking agents, see: Rajski, S. R.; Williams, R. M. Chem. Rev. 1998, 98, 2723-2796.
    • (1998) Chem. Rev. , vol.98 , pp. 2723-2796
    • Rajski, S.R.1    Williams, R.M.2


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.