The addition of TMSCN to carbonyl compounds catalyzed by K2CO3 as heterogeneous catalyst gave the corresponding cyanohydrin trimethylsilyl ethers from 20 minutes to 24 hours with 62% to 99% yields without solvent at room temperature. Moreover, it was found that chiral organic salts as heterogeneous catalysts also can catalyze the asymmetric version and afford the corresponding products with up to 99% yield and 12.4% ee
A simple and convenient method for the addition of TMSCN to carbonyl compounds is described. NbCl5 i...
AbstractDifferent amorphous mesoporous TUD-1 catalysts were employed in cyanosilylation of acetophen...
A novel family of Ln-N complexes was synthesized by two methods and as the Lewis acidic catalysts in...
Cyanohydrin trimethylsilyl ethers are versatile intermedi-ates for the synthesis of cyanohydrins, α-...
Dibenzyldimethyl ammonium bromide and triethanolamine N-oxide catalyze the formation of cyanohydrin ...
A variety of aldehydes and ketones were transformed to their corresponding cyanohydrin silyl ethers ...
Supported ionic liquid-like phases (SILLPs) are able to efficiently catalyse the cyanosilylation of ...
A new approach for the asymmetric addition of trimethylsilylcyanide to ketones using chiral N-oxide-...
Nucleophilic addition of TMSCN to carbonyl compounds is found to be catalysed efficiently using hydr...
Due to the high versatility of chiral cyanohydrins, the catalytic asymmetric cyanation reaction of c...
Cyanohydrin trimethylsilyl ethers are versatile intermedi-ates in the synthesis of α-hydroxy acids a...
Different amorphous mesoporous TUD-1 catalysts were employed in cyanosilylation of acetophenone with...
A novel chiral sulfoxide-containing ligand for the catalytic addition of trimethylsilylcyanide to al...
Tertiary cyanohydrin trimethylsilyl ethers were synthesized in excellent chemical yields by using sa...
Enantioselective addition of trimethylsilyl cyanide to ketones by a catalytic double-activation meth...
A simple and convenient method for the addition of TMSCN to carbonyl compounds is described. NbCl5 i...
AbstractDifferent amorphous mesoporous TUD-1 catalysts were employed in cyanosilylation of acetophen...
A novel family of Ln-N complexes was synthesized by two methods and as the Lewis acidic catalysts in...
Cyanohydrin trimethylsilyl ethers are versatile intermedi-ates for the synthesis of cyanohydrins, α-...
Dibenzyldimethyl ammonium bromide and triethanolamine N-oxide catalyze the formation of cyanohydrin ...
A variety of aldehydes and ketones were transformed to their corresponding cyanohydrin silyl ethers ...
Supported ionic liquid-like phases (SILLPs) are able to efficiently catalyse the cyanosilylation of ...
A new approach for the asymmetric addition of trimethylsilylcyanide to ketones using chiral N-oxide-...
Nucleophilic addition of TMSCN to carbonyl compounds is found to be catalysed efficiently using hydr...
Due to the high versatility of chiral cyanohydrins, the catalytic asymmetric cyanation reaction of c...
Cyanohydrin trimethylsilyl ethers are versatile intermedi-ates in the synthesis of α-hydroxy acids a...
Different amorphous mesoporous TUD-1 catalysts were employed in cyanosilylation of acetophenone with...
A novel chiral sulfoxide-containing ligand for the catalytic addition of trimethylsilylcyanide to al...
Tertiary cyanohydrin trimethylsilyl ethers were synthesized in excellent chemical yields by using sa...
Enantioselective addition of trimethylsilyl cyanide to ketones by a catalytic double-activation meth...
A simple and convenient method for the addition of TMSCN to carbonyl compounds is described. NbCl5 i...
AbstractDifferent amorphous mesoporous TUD-1 catalysts were employed in cyanosilylation of acetophen...
A novel family of Ln-N complexes was synthesized by two methods and as the Lewis acidic catalysts in...