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Volumn , Issue 6, 2007, Pages 0819-0823

Synthesis of 2-arylbenzothiazoles by DDQ-promoted cyclization of thioformanilides; a solution-phase strategy for library synthesis

Author keywords

2,6 dichloro 3,5 dicyano 1,4 benzoquinone; Benzothiazole; Cyclization; Solution phase; Sulfanyl radical; Thioformanilide

Indexed keywords

2,6-DICHLORO-3,5-DICYANO-1,4- BENZOQUINONE; BENZOTHIAZOLE; SOLUTION PHASE; SULFANYL RADICAL; THIOFORMANILIDE;

EID: 33947590756     PISSN: 00397881     EISSN: None     Source Type: Journal    
DOI: 10.1055/s-2007-965929     Document Type: Article
Times cited : (59)

References (41)
  • 6
    • 33947594478 scopus 로고    scopus 로고
    • Stevens, M. F. G.; Wells, G.; Westwell, A. D.; Poole, T. D. WO 03,004,479, 2003; Chem. Abstr., 2003, 138, 106698.
    • Stevens, M. F. G.; Wells, G.; Westwell, A. D.; Poole, T. D. WO 03,004,479, 2003; Chem. Abstr., 2003, 138, 106698.
  • 13
    • 33947572617 scopus 로고    scopus 로고
    • Klunk, W. E.; Mathis, C. A. Jr.; Wang, Y. WO 2004,083,195, 2004.
    • (b) Klunk, W. E.; Mathis, C. A. Jr.; Wang, Y. WO 2004,083,195, 2004.
  • 40
    • 33947587800 scopus 로고    scopus 로고
    • The material loss, as indicated by crude yields in Table 1, was mainly due to the binding of the product to the resin. In order to keep the same method as used in the final library synthesis, we did not use excessive solvent, which was limited by the of the collection plate, to wash the resin to improve the yields
    • The material loss, as indicated by crude yields in Table 1, was mainly due to the binding of the product to the resin. In order to keep the same method as used in the final library synthesis, we did not use excessive solvent, which was limited by the volume of the collection plate, to wash the resin to improve the yields


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.