Hydrosilanes are not always a reducing reagent: A ruthenium-catalyzed introduction of primary alkyl groups to electron-rich aromatic rings using esters as a source of the alkyl groups

Tetrahedron

Volumn 67, Issue 40, 2011, Pages 7667-7672

  Nagashima, Hideo ^a   Kubo, Yuichi ^a   Kawamura, Mitsunobu ^a   Nishikata, Takashi ^a   Motoyama, Yukihiro ^a  

^a KYUSHU UNIVERSITY   (Japan)

Author keywords

Alkylation; Ester; Hydrosilane; Reduction; Ruthenium cluster

Indexed keywords

1 (2 METHYLPROPYL) 2,4,6 TRIMETHOXYBENZENE; 1 (3 METHYLBUTYL) 2,4,6 TRIMETHOXYBENZENE; 1 (3 PHENYLPROPYL) 2,4,6 TRIMETHOXYBENZENE; 1 (4 BROMOBUTYL) 2,4,6 TRIMETHOXYBENZENE; 1 (4 CHLOROBUTYL) 2,4,6 TRIMETHOXYBENZENE; 1 (CYCLOHEXYLMETHYL) 2,4,6 TRIMETHOXYBENZENE; 1 (CYCLOPENTYLMETHYL) 2,4,6 TRIMETHOXYBENZENE; 1 ETHYL 2,4,6 TRIMETHOXYBENZENE; ALKYL GROUP; AROMATIC COMPOUND; BENZOIC ACID DERIVATIVE; BENZYL 2,4,6 TRIMETHOXYBENZENE; ESTER; HYDROSILANE DERIVATIVE; RUTHENIUM DERIVATIVE; SILANE DERIVATIVE; UNCLASSIFIED DRUG;

ARTICLE; CATALYSIS; PRIORITY JOURNAL;

EID: 84860389047     PISSN: 00404020     EISSN: 14645416     Source Type: Journal    
DOI: 10.1016/j.tet.2011.08.033     Document Type: Article

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