2002
DOI: 10.1016/s1381-1169(01)00297-7
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Silica immobilised palladium phosphine complexes as recyclable, regioselective catalysts for the allylic alkylation

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Cited by 14 publications
(11 citation statements)
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“…A widely studied approach to facilitate catalyst-product separation is the attachment of homogeneous catalysts to dendritic [11][12][13][14][15][16], or hybrid supports [17][18][19][20]. We have studied several approaches to obtain recyclable catalyst systems, including immobilization on various supports and two-phase catalysis [21][22][23][24][25][26][27][28][29][30]. As an important alternative we have been investigating the immobilization of catalysts to dendritic support.…”
Section: Introductionmentioning
confidence: 99%
“…A widely studied approach to facilitate catalyst-product separation is the attachment of homogeneous catalysts to dendritic [11][12][13][14][15][16], or hybrid supports [17][18][19][20]. We have studied several approaches to obtain recyclable catalyst systems, including immobilization on various supports and two-phase catalysis [21][22][23][24][25][26][27][28][29][30]. As an important alternative we have been investigating the immobilization of catalysts to dendritic support.…”
Section: Introductionmentioning
confidence: 99%
“…Under these pre-optimized conditions acetophenone gave 1,3diphenylpropan-1-one (26) in 83% yield, while 98% and 96% yields were achieved with 4-methyl (27) and penta-methyl (28) substituted acetophenones respectively, when benzyl alcohol was used as the alkylating agent. Unprotected hydroxy group was tolerated and the corresponding alkylated product 29 was obtained in 81% yield.…”
Section: Resultsmentioning
confidence: 99%
“…The first catalytic allylation reaction using a silica-based material was carried out by Sandee and co-workers in 2001. [46] They used palladium complexes coordinated by trialkoxysilanefunctionalized phosphine ligands decorated on MCM-41. This was used in the allylic alkylation of 3-phenyl-prop-2-enyl trifluoroacetate using sodium diethyl 2-methylmalonate as the nucleophile, which gave both linear (1-substitution without isomerization) and branched products (3-substitution with isomerization of the allylic portion) (Scheme 11).…”
Section: Silica-supported Pd Complex Catalystsmentioning
confidence: 99%
“…Silica-supported Pd complex with phosphine ligands for allylic substitution. [46] Scheme 12. PCNS-catalyzed tandem allylic alkylation and Pauson-Khand reaction.…”
Section: Silica-supported Pd Complex Catalystsmentioning
confidence: 99%