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Volumn , Issue 30, 2007, Pages 3204-3206

Development of a general route to periphery-functionalized azaborines and ladder-type azaborines by using common intermediates

Author keywords

[No Author keywords available]

Indexed keywords

AZABORINE; BROMINE DERIVATIVE; HETEROCYCLIC COMPOUND; UNCLASSIFIED DRUG;

EID: 34547444550     PISSN: 13597345     EISSN: None     Source Type: Journal    
DOI: 10.1039/b706418g     Document Type: Article
Times cited : (80)

References (24)
  • 22
    • 0034712161 scopus 로고    scopus 로고
    • tLi, 3b was recovered in 65% yield. Coordination of a butyl group to the boron center may prevent the halogen-lithium exchange reaction
    • J. P. Wolfe S. L. Buchwald J. Org. Chem. 2000 65 1144
    • (2000) J. Org. Chem. , vol.65 , pp. 1144
    • Wolfe, J.P.1    Buchwald, S.L.2
  • 23
    • 34547465847 scopus 로고    scopus 로고
    • t-carbazole, respectively, the generated amino-substituted ladder-type azaborine could not be isolated due to low solubility
    • t-carbazole, respectively, the generated amino-substituted ladder-type azaborine could not be isolated due to low solubility
  • 24
    • 34547484070 scopus 로고    scopus 로고
    • The results of the theoretical calculations are included in Electronic Supplementary Information
    • The results of the theoretical calculations are included in Electronic Supplementary Information


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.