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Volumn 73, Issue 16, 2008, Pages 6378-6381

Tandem Friedel-Crafts annulation to novel perylene analogues

Author keywords

[No Author keywords available]

Indexed keywords

CHEMICAL EQUATIONS; CORE PRODUCTS; FRIEDEL-CRAFTS; FRIEDEL-CRAFTS ALKYLATION; GOOD YIELDS; LEWIS ACIDS; NEW SERIES; OXIDATIVE AROMATIZATION; P-TOLUENE SULFONIC ACID; PERYLENE; ROOM TEMPERATURES; SULFOLANE; TETRAHYDRO NAPHTHALENE; TETRALIN; TETRALOL;

EID: 50149097039     PISSN: 00223263     EISSN: None     Source Type: Journal    
DOI: 10.1021/jo800558c     Document Type: Article
Times cited : (13)

References (46)
  • 3
    • 0000960150 scopus 로고
    • For review see
    • For review see: Langhals, H. Heterocycles 1995, 40, 477-500.
    • (1995) Heterocycles , vol.40 , pp. 477-500
    • Langhals, H.1
  • 21
    • 0042702139 scopus 로고    scopus 로고
    • Smith, H. M, Ed, Wiley-VCH: Weinheim, Germany
    • Greene, M. In High Performance Pigments; Smith, H. M., Ed.; Wiley-VCH: Weinheim, Germany, 2002; pp 249-262.
    • (2002) High Performance Pigments , pp. 249-262
    • Greene, M.1
  • 24
    • 50149089946 scopus 로고    scopus 로고
    • Eur. Pat. Appl. 2007, EP 1843407: Koenemann, M.; Pschirer, N. G.; Muellen, K.; Nolde, F.; Pisula, W.; Mueller, S.; Kohl, C. Chem. Abstr. 2007, 147, 460106.
    • (c) Eur. Pat. Appl. 2007, EP 1843407: Koenemann, M.; Pschirer, N. G.; Muellen, K.; Nolde, F.; Pisula, W.; Mueller, S.; Kohl, C. Chem. Abstr. 2007, 147, 460106.
  • 39
    • 50149101708 scopus 로고    scopus 로고
    • The acid catalyzed elimination of 2 to 3 occurs under mild conditions compared to the tandem Friedel-Crafts alkylations. Thus, it is possible that this reaction proceeds via the intermediacy of 3
    • The acid catalyzed elimination of 2 to 3 occurs under mild conditions compared to the tandem Friedel-Crafts alkylations. Thus, it is possible that this reaction proceeds via the intermediacy of 3.
  • 40
    • 0001759458 scopus 로고    scopus 로고
    • For detailed study of p-toluenesulfonic acid as Friedel-Crafts catalyst see: (a) Mahindaratne, M. P. D.; Wimalasena, K. J. Org. Chem. 1998, 63, 2858-2866.
    • For detailed study of p-toluenesulfonic acid as Friedel-Crafts catalyst see: (a) Mahindaratne, M. P. D.; Wimalasena, K. J. Org. Chem. 1998, 63, 2858-2866.
  • 41
    • 50149115937 scopus 로고    scopus 로고
    • Mahindaratne, M. P. D. Ph.D. Dissertation, Wichita State University, Wichita, KS, 2000.
    • (b) Mahindaratne, M. P. D. Ph.D. Dissertation, Wichita State University, Wichita, KS, 2000.
  • 42
    • 50149089553 scopus 로고    scopus 로고
    • For all crystallographic data of 4b see the Supporting Information, pp 13-24: (a) Crystal structure of 4b (page 13). (b) Molecular packing of the unit cell of 4b (page 13).
    • (a) For all crystallographic data of 4b see the Supporting Information, pp 13-24: (a) Crystal structure of 4b (page 13). (b) Molecular packing of the unit cell of 4b (page 13).
  • 43
    • 33845185705 scopus 로고
    • and references cited therein
    • Neumann, R.; Lissel, M. J. Org. Chem. 1989, 54, 4607-4610, and references cited therein.
    • (1989) J. Org. Chem , vol.54 , pp. 4607-4610
    • Neumann, R.1    Lissel, M.2


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.