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Volumn , Issue 10, 2009, Pages 1609-1613

Development and scope of the phenolic aldol reaction of 2-formylpyridines

Author keywords

2 formylpyridines; 2 hydroxyphenyl 2 pyridylmethanols; Arylation; Magnesium phenoxides; Phenolic aldol reaction

Indexed keywords

2 HYDROXYPHENYL 2 PYRIDYLMETHANE; 2 HYDROXYPHENYL 2 PYRIDYLMETHANOL; ELECTROPHILE; MAGNESIUM; PHENOL; PYRIDINE DERIVATIVE; UNCLASSIFIED DRUG;

EID: 67649385996     PISSN: 09365214     EISSN: 14372096     Source Type: Journal    
DOI: 10.1055/s-0029-1217325     Document Type: Article
Times cited : (5)

References (26)
  • 21
    • 67649328533 scopus 로고    scopus 로고
    • note
    • 2O on scale is complicated by its high volatility and flammability, MTBE is a much preferred alternative.
  • 22
    • 0000059198 scopus 로고    scopus 로고
    • 2 to promote selective orthoformylation of phenols, see
    • 2 to promote selective orthoformylation of phenols, see: (a) Hofslokken, N. U.; Skattebol, L. Acta Chem. Scand. 1999, 53, 258.
    • (1999) Acta Chem. Scand. , vol.53 , pp. 258
    • Hofslokken, N.U.1    Skattebol, L.2
  • 24
    • 30144431765 scopus 로고    scopus 로고
    • This becomes the main reaction pathway if phenol is omitted from the reaction mixture. For a recent report of a similar process, see
    • This becomes the main reaction pathway if phenol is omitted from the reaction mixture. For a recent report of a similar process, see: Abaee, M. S.; Sharifi, R.; Mojtahedi, M. M. Org. Lett. 2005, 7, 5893.
    • (2005) Org. Lett. , vol.7 , pp. 5893
    • Abaee, M.S.1    Sharifi, R.2    Mojtahedi, M.M.3
  • 25
    • 67649326054 scopus 로고    scopus 로고
    • note
    • 2, EtOH, EtOAc, i-PrOAc, 2-methyltetrahydrofuran, THF, α,α,α-trifluorotoluene, and sulfolane.
  • 26
    • 0041737791 scopus 로고    scopus 로고
    • 2 does not have a significant effect on the rate of the desired reduction but greatly reduces the rate of competitive dechlorination. For a report on the use of zinc halides to modulate the activity of hydrogenation catalysts, see
    • 2 does not have a significant effect on the rate of the desired reduction but greatly reduces the rate of competitive dechlorination. For a report on the use of zinc halides to modulate the activity of hydrogenation catalysts, see: Wu, G.; Huang, M.; Richards, M.; Poirier, M.; Wen, X.; Draper, R. W. Synthesis 2003, 1657.
    • (2003) Synthesis , pp. 1657
    • Wu, G.1    Huang, M.2    Richards, M.3    Poirier, M.4    Wen, X.5    Draper, R.W.6


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.