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Volumn 11, Issue 19, 2009, Pages 4290-4293

Chemoenzymatic access to versatile epoxyquinol synthons

Author keywords

[No Author keywords available]

Indexed keywords

BROMOXONE; CYCLOHEXENE DERIVATIVE; EPIEPOFORMIN; EPOXIDE; FUSED HETEROCYCLIC RINGS; HARVEYNONE; HEXACYCLINOL; HYDROQUINONE DERIVATIVE; PANEPOPHENANTHRIN; PHENANTHRENE DERIVATIVE; POLYCYCLIC HYDROCARBON;

EID: 70350140382     PISSN: 15237060     EISSN: None     Source Type: Journal    
DOI: 10.1021/ol9016657     Document Type: Article
Times cited : (48)

References (59)
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    • For a very useful introduction to this class of compound, see: (a) Marco-Contelles, J.; Molina, M. T.; Anjum, S. Chem. Rev. 2004, 104, 2857. For a discussion of certain related compounds, see:
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  • 6
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  • 14
    • 33746115758 scopus 로고    scopus 로고
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    • (2006) Org. Lett. , vol.8 , pp. 2895
    • Rychnovsky, S.D.1
  • 23
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    • See ref 11d [(+)-2]
    • (d) See ref 11d [(+)-2].
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    • See ref 11d [(+)-3]
    • (c) See ref 11d [(+)-3].
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    • See ref 12b [(+)-4]
    • (d) See ref 12b [(+)-4].
  • 34
    • 70350172401 scopus 로고    scopus 로고
    • See ref 6a and 6c (±)-6 and (+)-6, respectively
    • Syntheses of panepophenanthrin: (a) See ref 6a and 6c [(±)-6 and (+)-6, respectively.
  • 35
    • 70350183218 scopus 로고    scopus 로고
    • See ref 6b [(+)-6]
    • (b) See ref 6b [(+)-6],
  • 37
    • 70350184882 scopus 로고    scopus 로고
    • See ref 13d [(-)-6]
    • (d) See ref 13d [(-)-6].
  • 39
    • 70350205066 scopus 로고    scopus 로고
    • See ref 8 [(+)-9]
    • Syntheses of hexacyclinol: (a) See ref 8 [(+)-9].
  • 41
    • 70350195850 scopus 로고    scopus 로고
    • See refs 12b, 14a,b, 15a,b,e, and 16a,b for examples of the use of these types of cross-coupling processes
    • See refs 12b, 14a,b, 15a,b,e, and 16a,b for examples of the use of these types of cross-coupling processes.
  • 42
    • 70350205065 scopus 로고    scopus 로고
    • See refs 11a-c, 12a,e, 13b,d, 14a,b, 15c and 16b for examples of this type of approach
    • See refs 11a-c, 12a,e, 13b,d, 14a,b, 15c and 16b for examples of this type of approach.
  • 43
    • 70350208290 scopus 로고    scopus 로고
    • See refs 11b-d, 12a, 13b,d, 14b, 15a,c, and 16b for examples of this type of approach
    • See refs 11b-d, 12a, 13b,d, 14b, 15a,c, and 16b for examples of this type of approach.
  • 44
    • 70350184881 scopus 로고    scopus 로고
    • Compounds 10-12 can be obtained from Questor, Queen's University of Belfast, Northern Ireland. Questor Centre Contact Page: (accessed July 21, 2009)
    • Compounds 10-12 can be obtained from Questor, Queen's University of Belfast, Northern Ireland. Questor Centre Contact Page: http://questor.qub.ac. uk/newsite/contact.htm (accessed July 21, 2009).
  • 45
    • 0001846314 scopus 로고    scopus 로고
    • For reviews on methods for generating cis-1,2-dihydrocatechols by microbial dihydroxylation of the corresponding aromatics, as well as the synthetic applications of these metabolites, see: (a) Hudlicky, T.; Gonzalez, D.; Gibson, D. T. Aldrichim. Acta 1999, 32, 35.
    • (1999) Aldrichim. Acta , vol.32 , pp. 35
    • Hudlicky, T.1    Gonzalez, D.2    Gibson, D.T.3
  • 49
    • 70350197490 scopus 로고    scopus 로고
    • Details of these analyses are presented in the Supporting Information
    • Details of these analyses are presented in the Supporting Information.
  • 55
    • 70350186538 scopus 로고    scopus 로고
    • These previously unreported compounds were prepared from (trimethylstannyl)methanol using standard methods
    • These previously unreported compounds were prepared from (trimethylstannyl)methanol using standard methods.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.