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Volumn 13, Issue 2, 2011, Pages 232-235

Synthesis of benzodiquinanes via tandem palladium-catalyzed semipinacol rearrangement and direct arylation

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EID: 78651495411     PISSN: 15237060     EISSN: 15237052     Source Type: Journal    
DOI: 10.1021/ol1026415     Document Type: Article
Times cited : (50)

References (41)
  • 1
    • 78651483272 scopus 로고    scopus 로고
    • For reviews on traditional cross-coupling reactions, see
    • For reviews on traditional cross-coupling reactions, see
  • 4
    • 78651492445 scopus 로고    scopus 로고
    • For selected recent reviews on direct arylation, see
    • For selected recent reviews on direct arylation, see
  • 15
    • 70349900402 scopus 로고    scopus 로고
    • For a discussion, see:;, For examples of direct arylation with alkyl palladium(II) intermediates capable of β-hydride elimination see:; J. Org. Chem. 1994, 59, 33
    • For a discussion, see: René, O.; Lapointe, D.; Fagnou, K. Org. Lett. 2009, 11, 4560 For examples of direct arylation with alkyl palladium(II) intermediates capable of β-hydride elimination see: Song, Z. Z.; Wong, H. N. C. J. Org. Chem. 1994, 59, 33
    • (2009) Org. Lett. , vol.11 , pp. 4560
    • René, O.1    Lapointe, D.2    Fagnou, K.3    Song, Z.Z.4    Wong, H.N.C.5
  • 19
    • 78651516346 scopus 로고    scopus 로고
    • For examples of direct arylation using alkylpalladium intermediates generated from cyclobutanol fragmentation, see
    • For examples of direct arylation using alkylpalladium intermediates generated from cyclobutanol fragmentation, see
  • 21
    • 0035936747 scopus 로고    scopus 로고
    • For the analogous reaction using cyclobutanone oximes, see:; J. Am. Chem. Soc. 2000, 122, 12049
    • Nishimura, T.; Ohe, K.; Uemura, S. J. Org. Chem. 2001, 66, 1455 For the analogous reaction using cyclobutanone oximes, see: Nishimura, T.; Uemura, S. J. Am. Chem. Soc. 2000, 122, 12049
    • (2001) J. Org. Chem. , vol.66 , pp. 1455
    • Nishimura, T.1    Ohe, K.2    Uemura, S.3    Nishimura, T.4    Uemura, S.5
  • 23
    • 78651473656 scopus 로고    scopus 로고
    • Cascade Heck reaction
    • Cascade Heck reaction
  • 28
    • 78651513461 scopus 로고    scopus 로고
    • For a good entry into the metal homoenolate literature, see
    • For a good entry into the metal homoenolate literature, see
  • 33
    • 78651517176 scopus 로고    scopus 로고
    • This type of coordination of alkenylcyclobutanols has been invoked before; see
    • This type of coordination of alkenylcyclobutanols has been invoked before; see
  • 37
    • 78651511145 scopus 로고    scopus 로고
    • See Supporting Information for details
    • See Supporting Information for details.
  • 39
    • 78651485696 scopus 로고    scopus 로고
    • For an early example of palladium-catalyzed β-carboelimination of alkenyl-tert -cyclobutanols under oxidative conditions, see ref 5b. For a related rhodium-catalyzed C-C activation of allenyl-tert -cyclobutanols, see
    • For an early example of palladium-catalyzed β-carboelimination of alkenyl-tert -cyclobutanols under oxidative conditions, see ref 5b. For a related rhodium-catalyzed C-C activation of allenyl-tert -cyclobutanols, see


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.