A combination of sodium borohydride and a catalytic amount of indium(III) chloride in acetonitrile reduces exclusively the α,β -carbon-carbon double bond in α ,β ,γ ,δ -unsaturated diaryl ketones, dicarboxylic ester, cyanoester, and dicyano compounds
While alternative methods of preparing dichloroindium hydride (HInCl<sub>2</sub>) via the in situ re...
Sodium borohydride in ethylene glycol oligomers (PEGs) has been explored as a novel reducing system ...
It was shown that the hydrogenolysis of 4-acetyl-3α,4α-epoxycarane using NaBH4 is accomplished stere...
A combination of a catalytic amount of indium (III) chloride and sodium borohydride in acetonitrile ...
Indium hydride (Cl<SUB>2</SUB>InH) generated in situ from a combination of a catalytic amount of ind...
Indium metal in aqueous ethanolic ammonium chloride reduces the CC bond in highly activated conjugat...
Dichloroindium hydride (Cl2InH) generated in situ from the combination of a catalytic amount of indi...
A combination of sodium borohydride and a catalytic amount of indium(III) chloride in acetonitrile r...
Metal hydrides, since their inception, have proven to be invaluable to the organic chemist. As the c...
Formerly, our lab developed a one-pot synthesis for the reductive alkylation of monosubstituted malo...
Sodium borohydride (0.4–1.5 equivalents) in the presence of ammonium oxalate (0.2 equivalents) reduc...
A novel, efficient, and regio- as well as diastereoselective conversion of non-enolizable bicyclic α...
The reduction of aldehydes, ketones and carboxylic acid derivatives to the corresponding alcohols or...
α-Diketones are efficiently reduced with indium metal in methanol-water in the presence of NH4Cl, Li...
DDHQ/TCC esters 3a–f, 7a–g were prepared either by oxidation of spiroketones 1 with DDQ/Image -chlor...
While alternative methods of preparing dichloroindium hydride (HInCl<sub>2</sub>) via the in situ re...
Sodium borohydride in ethylene glycol oligomers (PEGs) has been explored as a novel reducing system ...
It was shown that the hydrogenolysis of 4-acetyl-3α,4α-epoxycarane using NaBH4 is accomplished stere...
A combination of a catalytic amount of indium (III) chloride and sodium borohydride in acetonitrile ...
Indium hydride (Cl<SUB>2</SUB>InH) generated in situ from a combination of a catalytic amount of ind...
Indium metal in aqueous ethanolic ammonium chloride reduces the CC bond in highly activated conjugat...
Dichloroindium hydride (Cl2InH) generated in situ from the combination of a catalytic amount of indi...
A combination of sodium borohydride and a catalytic amount of indium(III) chloride in acetonitrile r...
Metal hydrides, since their inception, have proven to be invaluable to the organic chemist. As the c...
Formerly, our lab developed a one-pot synthesis for the reductive alkylation of monosubstituted malo...
Sodium borohydride (0.4–1.5 equivalents) in the presence of ammonium oxalate (0.2 equivalents) reduc...
A novel, efficient, and regio- as well as diastereoselective conversion of non-enolizable bicyclic α...
The reduction of aldehydes, ketones and carboxylic acid derivatives to the corresponding alcohols or...
α-Diketones are efficiently reduced with indium metal in methanol-water in the presence of NH4Cl, Li...
DDHQ/TCC esters 3a–f, 7a–g were prepared either by oxidation of spiroketones 1 with DDQ/Image -chlor...
While alternative methods of preparing dichloroindium hydride (HInCl<sub>2</sub>) via the in situ re...
Sodium borohydride in ethylene glycol oligomers (PEGs) has been explored as a novel reducing system ...
It was shown that the hydrogenolysis of 4-acetyl-3α,4α-epoxycarane using NaBH4 is accomplished stere...