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Volumn 51, Issue 3, 2012, Pages 798-801

Palladium-catalyzed carbonylative α-arylation for accessing 1,3-diketones

Author keywords

1,3 diketones; carbonylation; homogeneous catalysis; isotope labeling; palladium

Indexed keywords

1,3-DIKETONES; ARYLATIONS; CARBON ISOTOPES; CORE STRUCTURE; DIRECT SYNTHESIS; HETEROCYCLIC COMPOUND; HOMOGENEOUS CATALYSIS; ISOTOPE LABELING;

EID: 84855812682     PISSN: 14337851     EISSN: 15213773     Source Type: Journal    
DOI: 10.1002/anie.201107494     Document Type: Article
Times cited : (82)

References (50)
  • 39
    • 0042704188 scopus 로고    scopus 로고
    • Palladium-catalyzed C-N couplings using LiHMDS as an ammonia surrogate have been described in the literature, see.
    • Palladium-catalyzed C-N couplings using LiHMDS as an ammonia surrogate have been described in the literature, see:, S. Lee, M. Jørgensen, J. F. Hartwig, Org. Lett. 2001, 3, 2729.
    • (2001) Org. Lett. , vol.3 , pp. 2729
    • Lee, S.1    Jørgensen, M.2    Hartwig, J.F.3
  • 40
    • 53349158722 scopus 로고    scopus 로고
    • It has been demonstrated that the aldol product from the condensation of aldehydes is reversible, releasing the reactive enolate intermediate by a retro-aldol process, see
    • It has been demonstrated that the aldol product from the condensation of aldehydes is reversible, releasing the reactive enolate intermediate by a retro-aldol process, see:, R. Martín, S. L. Buchwald, Angew. Chem. 2007, 119, 7374
    • (2007) Angew. Chem. , vol.119 , pp. 7374
    • Martín, R.1    Buchwald, S.L.2


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.