597-90-0Relevant articles and documents
Iridium-catalyzed regioselective silylation of secondary alkyl C-H bonds for the synthesis of 1,3-diols
Li, Bijie,Driess, Matthias,Hartwig, John F.
supporting information, p. 6586 - 6589 (2014/05/20)
We report Ir-catalyzed intramolecular silylation of secondary alkyl C-H bonds. (Hydrido)silyl ethers, generated in situ by dehydrogenative coupling of a tertiary or conformationally restricted secondary alcohol with diethylsilane, undergo regioselective silylation at a secondary C-H bond Υ to the hydroxyl group. Oxidation of the resulting oxasilolanes in the same vessel generates 1,3-diols. This method provides a strategy to synthesize 1,3-diols through a hydroxyl-directed, functionalization of secondary alkyl C-H bonds. Mechanistic studies suggest that the C-H bond cleavage is the turnover-limiting step of the catalytic cycle. This silylation of secondary C-H bonds is only 40-50 times slower than the analogous silylation of primary C-H bonds.
Primary, secondary and tertiary alkylamines α,α-N-disubstituted synthesis and pharmacology
Pigerol,Vernieres,Broll,et al.
, p. 351 - 359 (2007/10/05)
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