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Volumn 132, Issue 46, 2010, Pages 16340-16342

Electrophilic aromatic substitution of a BN indole

Author keywords

[No Author keywords available]

Indexed keywords

BOND DISTANCE; BORON ATOM; ELECTROPHILIC AROMATIC SUBSTITUTIONS; INDOLE DERIVATIVES; X RAY STRUCTURAL ANALYSIS;

EID: 78649291902     PISSN: 00027863     EISSN: 15205126     Source Type: Journal    
DOI: 10.1021/ja107312u     Document Type: Article
Times cited : (56)

References (44)
  • 3
    • 78649260761 scopus 로고    scopus 로고
    • For leading references, see
    • For leading references, see
  • 13
    • 78649315227 scopus 로고    scopus 로고
    • For pioneering work in this area, see
    • For pioneering work in this area, see
  • 16
    • 78649298790 scopus 로고    scopus 로고
    • For an overview, see
    • For an overview, see
  • 18
    • 78649268436 scopus 로고    scopus 로고
    • For a review of tryptophan biosynthesis, see
    • For a review of tryptophan biosynthesis, see
  • 24
    • 78649256549 scopus 로고    scopus 로고
    • For an overview, see
    • For an overview, see
  • 28
    • 78649271023 scopus 로고    scopus 로고
    • For an overview on 2,3-dihydro-1 H -1,3,2-diazaboroles, see
    • For an overview on 2,3-dihydro-1 H -1,3,2-diazaboroles, see
  • 31
    • 78649242752 scopus 로고    scopus 로고
    • To the best of our knowledge, EAS reactions have not been demonstrated with 2,3-dihydro-1 H -1,3,2-diazaboroles.
    • To the best of our knowledge, EAS reactions have not been demonstrated with 2,3-dihydro-1 H -1,3,2-diazaboroles.
  • 35
    • 78649251276 scopus 로고    scopus 로고
    • The determination of the substitution pattern for 6b and 6d were made by inference.
    • The determination of the substitution pattern for 6b and 6d were made by inference.
  • 38
    • 78649288657 scopus 로고    scopus 로고
    • Correspondence concerning X-ray crystallography should be directed to Lev Zakharov. E-mail: lev@uoregon.edu.
    • Correspondence concerning X-ray crystallography should be directed to Lev Zakharov. E-mail: lev@uoregon.edu.
  • 39
    • 78649285897 scopus 로고    scopus 로고
    • Although we have determined that trimer 7 is the major product in the acid catalyzed trimerization of 2, we were not able to isolate 7 cleanly. See Supporting Information for details.
    • Although we have determined that trimer 7 is the major product in the acid catalyzed trimerization of 2, we were not able to isolate 7 cleanly. See Supporting Information for details.
  • 41
    • 78649268013 scopus 로고    scopus 로고
    • For a representative example, see the structure published in
    • For a representative example, see the structure published in
  • 44
    • 78649309125 scopus 로고    scopus 로고
    • See Supporting Information for details.
    • See Supporting Information for details.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.