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Volumn 69, Issue 22, 2004, Pages 7761-7764

Synthesis of novel KDR kinase inhibitors through catalytic reductive cyclization of o-nitrobenzylcarbonyl compounds

Author keywords

[No Author keywords available]

Indexed keywords

CATALYSIS; ENZYME INHIBITION; ETHANOL; HYDROLYSIS; OPTIMIZATION; OXIDATION; REDUCTION; SYNTHESIS (CHEMICAL);

EID: 6344263852     PISSN: 00223263     EISSN: None     Source Type: Journal    
DOI: 10.1021/jo048843m     Document Type: Article
Times cited : (39)

References (41)
  • 9
    • 6344269900 scopus 로고
    • Houlihan, W. J., Ed.; Wiley-Interscience: New York, Chapter 2
    • (b) Brown, R. K. In Indoles; Houlihan, W. J., Ed.; Wiley-Interscience: New York, 1972; Part 1, Chapter 2.
    • (1972) Indoles , Issue.PART 1
    • Brown, R.K.1
  • 32
    • 6344268776 scopus 로고    scopus 로고
    • German Patent DE828695, 1950
    • Jacob, R. M. German Patent DE828695, 1950.
    • Jacob, R.M.1
  • 36
    • 85082551132 scopus 로고
    • and references therein
    • For the chlorination of ketones under Swern oxidation conditions, see: Tidwell, T. T. Synthesis 1990, 857 and references therein.
    • (1990) Synthesis , pp. 857
    • Tidwell, T.T.1
  • 39
    • 6344274759 scopus 로고    scopus 로고
    • note
    • 2O, which yielded 12 in 65% yield. See the Supporting Information.
  • 40
    • 6344269611 scopus 로고    scopus 로고
    • note
    • We speculate that hydroxyl indole 13 arises by cyclization on a hydroxylamine intermediate 20 onto the adjacent ketone.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.