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Most Requested Journal Articles 3Q05-Chemistry and Related Science
Following is one of the journal articles most requested by researchers using CAS electronic products.
CAPLUS COPYRIGHT 2005 ACS on STN
It was found that the chemoselectivity could be completely switched from C:O to C:C bonds in the transfer hydrogenation of activated .alpha.,.beta.-unsatd. ketones R1CH:CR2COR3 (R1 = Ph, 4-MeOC6H4, 4-O2NC6H4; R2 = H, Me, MeCO, EtO2C; R3 = Me, Ph) catalyzed by diamine-ruthenium complex. Moreover, this addn. via metal hydride had been applied to the redn. of various activated olefins R4R5C:CR6R7 (R4 = H, Me; R5 = H, n-C5H11, Ph, 4-MeOC6H4, 4-O2NC6H4; R6 = CN, EtO2C, Ph, O2N, etc.; R7 = H, CN, O2N, HO2C, etc.). The electron-withdrawing ability of functional groups substituted on C:C bonds at the .alpha.- or .beta.-position had strong influence on the reactivity. In addn., a wide variety of chiral diamine-Ru(II)(arene) systems was investigated to explore the asym. transfer hydrogenation of prochiral .alpha.,.alpha.-dicyanoolefins. Two parameters had been systematically studied: (i) the structure of the N-sulfonylated chiral diamine ligands and (ii) the structure of the metal precursors.
View full-text pdf document from the American Chemical Society, a participating ChemPort publisher. Updated 5/9/2007 2:51:52 PM
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