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Volumn 49, Issue 1, 2008, Pages 149-152

Studies on isocyanides: synthesis of tetrazolyl-isoindolinones via tandem Ugi four-component condensation/intramolecular amidation

Author keywords

[No Author keywords available]

Indexed keywords

2 (4 CHLORO)BENZYL 3 (1 CYCLOHEXYL 1H TETRAZOL) 5 YL 2,3 DIHYDRO 1H ISOINDOL 1 ONE; 3 (1 BENZYL 1H TETRAZOL) 5 YL 2,3 DIHYDRO 2 (4 METHYL)PHENYL 1H ISOINDOL 1 ONE; 3 [1 (4 ETHOXY)PHENYL 1H TETRAZOL] 5 YL 2,3 DIHYDRO 2 METHYL 1H ISOINDOL 1 ONE; 4 CHLOROBENZYLAMINE; 4 TOLUIDINE; ANILINE DERIVATIVE; AZIDE; BENZOIC ACID DERIVATIVE; CYANIDE; ETHOXIDE SODIUM; ISOINDOLE DERIVATIVE; METHYL 2 [(1 BENZYL 1H TETRAZOL) 5 YL (4 METHYLPHENYL)AMINO]METHYLBENZOATE; METHYLAMINE; SODIUM DERIVATIVE; TRIMETHYLSILYLAZIDE; UNCLASSIFIED DRUG;

EID: 36549070069     PISSN: 00404039     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.tetlet.2007.10.154     Document Type: Article
Times cited : (52)

References (44)
  • 1
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    • Katritzky A.R., Rees C.W., and Scriven E.F.V. (Eds), Pergamon, Oxford
    • Butler R.N. In: Katritzky A.R., Rees C.W., and Scriven E.F.V. (Eds). Comprehensive Heterocyclic Chemistry II Vol. 4 (1996), Pergamon, Oxford 621-678
    • (1996) Comprehensive Heterocyclic Chemistry II , vol.4 , pp. 621-678
    • Butler, R.N.1
  • 35
    • 84890574887 scopus 로고    scopus 로고
    • Post-condensation Modifications of the Passerini and Ugi Reactions
    • Zhu J., and Bienaymé H. (Eds), Wiley-VCH, Weinheim
    • Marcaccini S., and Torroba T. Post-condensation Modifications of the Passerini and Ugi Reactions. In: Zhu J., and Bienaymé H. (Eds). Multicomponent Reactions (2005), Wiley-VCH, Weinheim 33-75
    • (2005) Multicomponent Reactions , pp. 33-75
    • Marcaccini, S.1    Torroba, T.2
  • 39
    • 36649014266 scopus 로고    scopus 로고
    • While the manuscript was in preparation a paper dealing with the use of 2-formylbenzoic esters as bireactive materials for the synthesis of quinoline-based tetracycles via isocyanide multicomponent reaction appeared: Che, C.; Xiang, J.; Wang, G.-X.; Fathi, R.; Quan, J.-M.; Yang, Z. J. Comb. Chem., Web release date: 18 August 2007, doi:10.1021/cc070058a.
  • 40
    • 0038741823 scopus 로고    scopus 로고
    • 3 (1:1) with ethereal diazomethane at 0 °C
    • 3 (1:1) with ethereal diazomethane at 0 °C
    • (2003) Tetrahedron , vol.59 , pp. 3593-3601
    • Ye, B.-H.1    Naruta, Y.2
  • 42
    • 36549039358 scopus 로고    scopus 로고
    • note
    • 2: C, 69.72; H, 5.61; N, 16.94. Found: C, 69.89; H, 5.51; N, 17.03. Ugi adducts 5b-d were prepared in the same manner.
  • 43
    • 36549082706 scopus 로고    scopus 로고
    • note
    • 2: C, 64.47; H, 5.11; N, 20.88. Found: C, 64.29; H, 5.21; N, 21.05.
  • 44
    • 36549068519 scopus 로고    scopus 로고
    • note
    • 5O: C, 72.42; H, 5.02; N, 18.36. Found: C, 72.46; H, 4.90; N, 18.59. Compounds 6b-d were prepared in a similar manner.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.