A convenient, mild and simple procedure, employing sodium cyanoborohydride in the presence of either catalytic or stoichiometric amount of boron trifluoride etherate in dry THF, for the reductive cleavage of the acetals and ketals is described
Formerly, our lab developed a one-pot synthesis for the reductive alkylation of monosubstituted malo...
Azo compounds, both symmetrical and unsymmetrical are cleaved to amine/s by using Raney nickel and a...
A regioselective reductive demethoxylation of alkyl methyl ketals employing sodium cyanoborohydride ...
A convenient, mild and simple procedure, employing sodium cyanoborohydride in the presence of either...
A convenient, mild and simple procedure, employing sodium cyanoborohydride in the presence of either...
A regioselective reductive demethoxylation of dimethyl and mixed ketals, using sodium cyanoborohydri...
A regioselective reductive demethoxylation of dimethyl and mixed ketals, using sodium cyanoborohydri...
A one step, clean and efficient, conversion of arylaldehydes, ketones and ketals into the correspond...
A one step, clean and efficient, conversion of arylaldehydes, ketones and ketals into the correspond...
A regioselective reductive demethoxylation of dimethyl and mixed ketals, using sodium cyanoborohydri...
International audienceA protocol is described for the reductive cleavage of the C–O bond of aromatic...
A simple and convenient procedure for a highly chemoselective reductive deoxygenation of alpha,beta-...
A simple and convenient procedure for a highly chemoselective reductive deoxygenation of alpha,beta-...
A simple and convenient procedure for a highly chemoselective reductive deoxygenation of α,β-unsatur...
Treatment of acetals with bismuth(III) chloride in methanol provides a simple, convenient and chemos...
Formerly, our lab developed a one-pot synthesis for the reductive alkylation of monosubstituted malo...
Azo compounds, both symmetrical and unsymmetrical are cleaved to amine/s by using Raney nickel and a...
A regioselective reductive demethoxylation of alkyl methyl ketals employing sodium cyanoborohydride ...
A convenient, mild and simple procedure, employing sodium cyanoborohydride in the presence of either...
A convenient, mild and simple procedure, employing sodium cyanoborohydride in the presence of either...
A regioselective reductive demethoxylation of dimethyl and mixed ketals, using sodium cyanoborohydri...
A regioselective reductive demethoxylation of dimethyl and mixed ketals, using sodium cyanoborohydri...
A one step, clean and efficient, conversion of arylaldehydes, ketones and ketals into the correspond...
A one step, clean and efficient, conversion of arylaldehydes, ketones and ketals into the correspond...
A regioselective reductive demethoxylation of dimethyl and mixed ketals, using sodium cyanoborohydri...
International audienceA protocol is described for the reductive cleavage of the C–O bond of aromatic...
A simple and convenient procedure for a highly chemoselective reductive deoxygenation of alpha,beta-...
A simple and convenient procedure for a highly chemoselective reductive deoxygenation of alpha,beta-...
A simple and convenient procedure for a highly chemoselective reductive deoxygenation of α,β-unsatur...
Treatment of acetals with bismuth(III) chloride in methanol provides a simple, convenient and chemos...
Formerly, our lab developed a one-pot synthesis for the reductive alkylation of monosubstituted malo...
Azo compounds, both symmetrical and unsymmetrical are cleaved to amine/s by using Raney nickel and a...
A regioselective reductive demethoxylation of alkyl methyl ketals employing sodium cyanoborohydride ...
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