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Volumn , Issue 13, 2009, Pages 2198-2200

Palladium-catalyzed Mizoroki-Heck-type reaction of aryl trimethoxysilanes

Author keywords

Alkenes; Aryltrimethoxysilanes; Cross coupling; Heck reaction; Palladium catalyzed

Indexed keywords

ALKENE; ARSENIC DERIVATIVE; ARSENIC TRIMETHOXYSILANE; PALLADIUM; POLYCYCLIC AROMATIC HYDROCARBON DERIVATIVE; SILANE DERIVATIVE; UNCLASSIFIED DRUG;

EID: 68949147027     PISSN: 09365214     EISSN: 14372096     Source Type: Journal    
DOI: 10.1055/s-0029-1217571     Document Type: Article
Times cited : (15)

References (52)
  • 42
    • 14344266665 scopus 로고    scopus 로고
    • de Mejijere, A, Diederich, F, Eds, Wiley-VCH: Weinheim
    • (a) Mitchell, T. N. In Metal-Catalyzed Cross-Coupling Reactions, Vol. 1; de Mejijere, A.; Diederich, F., Eds.; Wiley-VCH: Weinheim, 2004, 125-162.
    • (2004) Metal-Catalyzed Cross-Coupling Reactions , vol.1 , pp. 125-162
    • Mitchell, T.N.1
  • 44
    • 0035980292 scopus 로고    scopus 로고
    • For oxidative Mizoroki-Heck-type reactions of aryl silanol, see: a
    • For oxidative Mizoroki-Heck-type reactions of aryl silanol, see: (a) Mori, A.; Danda, Y.; Fujii, T.; Hirabayashi, K.; Osakada, K. J. Am. Chem. Soc. 2001, 123, 10774.
    • (2001) J. Am. Chem. Soc , vol.123 , pp. 10774
    • Mori, A.1    Danda, Y.2    Fujii, T.3    Hirabayashi, K.4    Osakada, K.5
  • 52
    • 68949085996 scopus 로고    scopus 로고
    • 2 (2.2 mg, 5 mol%), 1,10-phenanthroline (3.6 mg, 10 mol%), AgF (76 mg, 0.6 mmol) and DMF (2 mL). The mixture was stirred at 60°C. After completion of the reaction (monitored by TLC), EtOAc (20 mL) was added and the mixture was washed with water (10 x 3 mL). Then the organic layer was dried, concentrated in vacuo and the residue was purified by flash column chromatography on a silica gel to give the desired product.
    • 2 (2.2 mg, 5 mol%), 1,10-phenanthroline (3.6 mg, 10 mol%), AgF (76 mg, 0.6 mmol) and DMF (2 mL). The mixture was stirred at 60°C. After completion of the reaction (monitored by TLC), EtOAc (20 mL) was added and the mixture was washed with water (10 x 3 mL). Then the organic layer was dried, concentrated in vacuo and the residue was purified by flash column chromatography on a silica gel to give the desired product.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.