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Volumn 63, Issue 4, 2007, Pages 910-917

Reaction of chromone-3-carbaldehyde with α-amino acids-syntheses of 3- and 4-(2-hydroxybenzoyl)pyrroles

Author keywords

1,3 Dipolar cycloadditions; 1,5 Electrocyclizations; Azomethine ylides; Benzoylpyrroles; Chromones

Indexed keywords

3 (2 HYDROXYBENZOYL)PYRROLE; 4 (2 HYDROXYBENZOYL)PYRROLE; ALDEHYDE DERIVATIVE; ALPHA AMINO ACID; AMINO ACID DERIVATIVE; AZOMETHINE YLIDE; CHROMONE 3 CARBALDEHYDE; CHROMONE DERIVATIVE; GLYCINE DERIVATIVE; METHYL GLYCINATE; PYRIDINE; PYRROLE; PYRROLE DERIVATIVE; PYRROLIDINE DERIVATIVE; XANTHENE DERIVATIVE;

EID: 33845452005     PISSN: 00404020     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.tet.2006.11.034     Document Type: Article
Times cited : (30)

References (31)
  • 12
    • 0004267670 scopus 로고
    • Jones R.A. (Ed), Wiley, New York, NY Part I
    • In: Jones R.A. (Ed). Pyrroles (1990), Wiley, New York, NY Part I
    • (1990) Pyrroles
  • 14
    • 33845409903 scopus 로고    scopus 로고
    • For other examples of 1,5-electrocyclization reactions of azomethine ylides to afford pyrroles, see:
  • 16
    • 33845439183 scopus 로고    scopus 로고
    • For other examples of 1,5-electrocyclization reactions of azomethine ylides, see:
  • 19
    • 33845401482 scopus 로고    scopus 로고
    • note
    • 6
  • 21
    • 33845437767 scopus 로고    scopus 로고
    • For the reaction of chromone 1 with other 1,3-dipoles, namely diazomethane, see:
  • 23
    • 33845391657 scopus 로고    scopus 로고
    • The deformylation of other derivatives of chromone 1 has already been reported.
  • 27
    • 33845395634 scopus 로고    scopus 로고
    • note
    • 16
  • 29
    • 84986444089 scopus 로고
    • Pyrrole 12 was previously prepared in two steps, in 30% global yield, from the reaction of 1 with N-benzoylglycine (hippuric acid), followed by treatment of the resulting azlactone with methanolic sodium carbonate.
    • Pyrrole 12 was previously prepared in two steps, in 30% global yield, from the reaction of 1 with N-benzoylglycine (hippuric acid), followed by treatment of the resulting azlactone with methanolic sodium carbonate. Fitton A.O., Frost J.R., Suschitzky H., and Houghoton P.G. Synthesis (1977) 133-135
    • (1977) Synthesis , pp. 133-135
    • Fitton, A.O.1    Frost, J.R.2    Suschitzky, H.3    Houghoton, P.G.4
  • 30
    • 33845443005 scopus 로고    scopus 로고
    • note
    • 16


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.