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Volumn 12, Issue 15, 2010, Pages 3324-3327

Synthesis of antimicrobial natural products targeting FtsZ: (+)-totarol and related totarane diterpenes

Author keywords

[No Author keywords available]

Indexed keywords

ANTIINFECTIVE AGENT; BACTERIAL PROTEIN; BIOLOGICAL PRODUCT; CYTOSKELETON PROTEIN; DITERPENE; FTSZ PROTEIN, BACTERIA; TOTARADIOL; TOTAROL; TOTAROLONE;

EID: 77955138547     PISSN: 15237060     EISSN: 15237052     Source Type: Journal    
DOI: 10.1021/ol100929z     Document Type: Article
Times cited : (44)

References (69)
  • 7
    • 77955134793 scopus 로고    scopus 로고
    • Indirect techniques, including site-directed mutagenesis and mapping of mutations to resistant strains, have provided evidence for the mode of inactivation of one FtsZ inhibitor
    • Indirect techniques, including site-directed mutagenesis and mapping of mutations to resistant strains, have provided evidence for the mode of inactivation of one FtsZ inhibitor
  • 13
    • 77955153176 scopus 로고    scopus 로고
    • Curcumin has been reported to target many proteins, including both FtsZ and tubulin
    • Curcumin has been reported to target many proteins, including both FtsZ and tubulin
  • 16
    • 77955157673 scopus 로고    scopus 로고
    • Much of the history of totarol has been reviewed, see
    • Much of the history of totarol has been reviewed, see
  • 18
    • 65549154229 scopus 로고    scopus 로고
    • (accessed on Aug 16, 2009
    • Nixon, D.; Hobbs, D. NZ Family Phys. 2006, 33, 253-255, http://www.cosmeticsdesign.com/Formulation-Science/Totarol-goes-global (accessed on Aug 16, 2009
    • (2006) NZ Family Phys. , vol.33 , pp. 253-255
    • Nixon, D.1    Hobbs, D.2
  • 26
    • 41549134341 scopus 로고    scopus 로고
    • Additional synthetic work is described in ref 6
    • Tada, M.; Kurabe, J.; Yasue, H.; Ikuta, T. Chem. Pharm. Bull. 2008, 56, 287-291 Additional synthetic work is described in ref 6.
    • (2008) Chem. Pharm. Bull. , vol.56 , pp. 287-291
    • Tada, M.1    Kurabe, J.2    Yasue, H.3    Ikuta, T.4
  • 47
    • 77955166788 scopus 로고    scopus 로고
    • A high level of steric control has been observed in a substrate related to 4 that is shorter by one carbon between the phenyl ring and the central alkene, see
    • A high level of steric control has been observed in a substrate related to 4 that is shorter by one carbon between the phenyl ring and the central alkene, see
  • 54
    • 33845558756 scopus 로고
    • These conditions were optimized for execution in a microwave reactor. See the Supporting Information
    • Kaplan, L. J.; Weisman, G. R.; Cram, D. J. J. Org. Chem. 1979, 44, 2226-2233 These conditions were optimized for execution in a microwave reactor. See the Supporting Information.
    • (1979) J. Org. Chem. , vol.44 , pp. 2226-2233
    • Kaplan, L.J.1    Weisman, G.R.2    Cram, D.J.3
  • 55
    • 77955167269 scopus 로고    scopus 로고
    • Use of the Grignard reagent was reported by Nishizawa and co-workers. Although the preparation does not appear in the experimental section of this publication, the procedure was provided to us by Prof. Nishizawa, see
    • Use of the Grignard reagent was reported by Nishizawa and co-workers. Although the preparation does not appear in the experimental section of this publication, the procedure was provided to us by Prof. Nishizawa, see
  • 57
    • 77955154554 scopus 로고    scopus 로고
    • In one run, 18 was isolated as an mixture with bromide 16a and 17 (from protonation of 6a) in 43% yield
    • In one run, 18 was isolated as an mixture with bromide 16a and 17 (from protonation of 6a) in 43% yield.
  • 62
    • 77955157672 scopus 로고    scopus 로고
    • Enantiomeric excess was determined by chiral HPLC after cyclization to 24 (Scheme 3). See the Supporting Information for details
    • Enantiomeric excess was determined by chiral HPLC after cyclization to 24 (Scheme 3). See the Supporting Information for details.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.