Add to ORKGA simple and convenient procedure for a highly chemoselective reductive deoxygenation of alpha,beta-unsaturated ketones and allyl alcohols to olefins by sodium cyanoborohydride and boron trifluoride etherate in dry THF is described
Formerly, our lab developed a one-pot synthesis for the reductive alkylation of monosubstituted malo...
The condensation of boron stabilised carbanions, Mes2BCHLiR1, (R1≠H) with aliphatic aldehydes, R2CHO...
A combination of pentafluorophenylboronic acid and oxalic acid catalyses the dehydrative substitutio...
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...
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 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 variety of structurally different aldehydes undergo chemoselectire reduction over ketones with zin...
A convenient, mild and simple procedure, employing sodium cyanoborohydride in the presence of either...
The combination of sodium borohydride and amberlyst-15 (H+) in tetrahydrofurane is a powerful reduct...
Treatment of bromoketals 2, derived from allyl alcohols 1, with tributyltin chloride, sodium cyanobo...
Treatment of bromoketals 2, derived from allyl alcohols 1, with tributyltin chloride, sodium cyanobo...
Sodium borohydride (0.4–1.5 equivalents) in the presence of ammonium oxalate (0.2 equivalents) reduc...
Formerly, our lab developed a one-pot synthesis for the reductive alkylation of monosubstituted malo...
The condensation of boron stabilised carbanions, Mes2BCHLiR1, (R1≠H) with aliphatic aldehydes, R2CHO...
A combination of pentafluorophenylboronic acid and oxalic acid catalyses the dehydrative substitutio...
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...
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 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 variety of structurally different aldehydes undergo chemoselectire reduction over ketones with zin...
A convenient, mild and simple procedure, employing sodium cyanoborohydride in the presence of either...
The combination of sodium borohydride and amberlyst-15 (H+) in tetrahydrofurane is a powerful reduct...
Treatment of bromoketals 2, derived from allyl alcohols 1, with tributyltin chloride, sodium cyanobo...
Treatment of bromoketals 2, derived from allyl alcohols 1, with tributyltin chloride, sodium cyanobo...
Sodium borohydride (0.4–1.5 equivalents) in the presence of ammonium oxalate (0.2 equivalents) reduc...
Formerly, our lab developed a one-pot synthesis for the reductive alkylation of monosubstituted malo...
The condensation of boron stabilised carbanions, Mes2BCHLiR1, (R1≠H) with aliphatic aldehydes, R2CHO...
A combination of pentafluorophenylboronic acid and oxalic acid catalyses the dehydrative substitutio...