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Volumn 72, Issue 16, 2007, Pages 6280-6283

Efficient access to orthoquinols and their [4 + 2] cyclodimers via SIBX-mediated hydroxylative phenol dearomatization

Author keywords

[No Author keywords available]

Indexed keywords

AROMATIZATION; DIMERS; HYDROXYLATION; IODINE; PHENOLS;

EID: 34547623434     PISSN: 00223263     EISSN: None     Source Type: Journal    
DOI: 10.1021/jo0708893     Document Type: Article
Times cited : (71)

References (35)
  • 1
    • 0042291889 scopus 로고    scopus 로고
    • Astruc, D, Ed, Wiley-VCH: Weinheim
    • (a) Quideau, S. In Modern Arene Chemistry; Astruc, D., Ed.; Wiley-VCH: Weinheim, 2002; pp 539-573.
    • (2002) Modern Arene Chemistry , pp. 539-573
    • Quideau, S.1
  • 5
  • 13
    • 34547615524 scopus 로고    scopus 로고
    • Depernet, D.; Francois, B. WO, 02/ 057210 A1, U.S. 2002/0107416, PCT/FR02/00189.
    • (b) Depernet, D.; Francois, B. WO, 02/ 057210 A1, U.S. 2002/0107416, PCT/FR02/00189.
  • 19
    • 33748241665 scopus 로고    scopus 로고
    • This dimer is a metabolite of the bacterial degradation of 7a. See: Kneifel, H, Poszich-Busher, C, Rittich, S, Breitmaier, E. Angew. Chem, Int. Ed. 1991, 30, 202-203
    • This dimer is a metabolite of the bacterial degradation of 7a. See: Kneifel, H.; Poszich-Busher, C.; Rittich, S.; Breitmaier, E. Angew. Chem., Int. Ed. 1991, 30, 202-203.
  • 24
    • 17844401197 scopus 로고    scopus 로고
    • For reaction and purification conditions better suited for the preparation of catechols via IBX-mediated oxygenation of phenols, see: (a) Pezzella, A, Lista, L, Napolitano, A, d'Ischia, M. Tetrahedron Lett. 2005, 46, 3541-3544
    • For reaction and purification conditions better suited for the preparation of catechols via IBX-mediated oxygenation of phenols, see: (a) Pezzella, A.; Lista, L.; Napolitano, A.; d'Ischia, M. Tetrahedron Lett. 2005, 46, 3541-3544.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.