The development of a novel, chemoselective, and catalytic deprotection methodology that proceeds under mild and neutral conditions is described, and its mechanism of action is analyzed in some detail. The scope, limitations, and advantages of this protocol are discussed. Selected applications in synthesis are also highlighted
A simple, mild and efficient method for deprotection of acetonides in the presence of molecular iodi...
813-814Trimethylsilyl ethers are selectively and rapidly oxidized to the corresponding carbonyl comp...
A variety of thioacetals and dithianes are deprotected into their carbonyl compounds in mild conditi...
The development of a novel, chemoselective, and catalytic deprotection methodology that proceeds und...
The development of a novel, chemoselective, and catalytic deprotection methodology that proceeds und...
Smooth and quantitative deprotection of a wide range of acetals and ketals [Eq. (a); R, R(1)=alkyl, ...
The chemoselective, catalytic deprotection of a variety of ketals, THP, and selected silyl ethers ca...
Cerium(IV) ammonium nitrate (CAN) is a powerful, though mild, reagent for the efficient and selectiv...
The catalytic deprotection of a range of functionalised THP and THF ethers can be efficiently perfor...
707-709Highly chemoselective deprotection of diacetone sugars have been achieved at room temperature...
A simple and mild procedure for the efficient deprotection of cyclic acetals and ketals, using ceriu...
The regioselective introduction of a methoxymethyl (MOM) group on different type of glycols via an o...
The electrophilicity of the carbonyl group is a dominant feature of its extensive chemistry. A major...
Ytterbium triflate catalyses the deprotection of tert-butyl esters selectively in the presence of ot...
Ytterbium triflate catalyses the deprotection of tert-butyl esters selectively in the presence of ot...
A simple, mild and efficient method for deprotection of acetonides in the presence of molecular iodi...
813-814Trimethylsilyl ethers are selectively and rapidly oxidized to the corresponding carbonyl comp...
A variety of thioacetals and dithianes are deprotected into their carbonyl compounds in mild conditi...
The development of a novel, chemoselective, and catalytic deprotection methodology that proceeds und...
The development of a novel, chemoselective, and catalytic deprotection methodology that proceeds und...
Smooth and quantitative deprotection of a wide range of acetals and ketals [Eq. (a); R, R(1)=alkyl, ...
The chemoselective, catalytic deprotection of a variety of ketals, THP, and selected silyl ethers ca...
Cerium(IV) ammonium nitrate (CAN) is a powerful, though mild, reagent for the efficient and selectiv...
The catalytic deprotection of a range of functionalised THP and THF ethers can be efficiently perfor...
707-709Highly chemoselective deprotection of diacetone sugars have been achieved at room temperature...
A simple and mild procedure for the efficient deprotection of cyclic acetals and ketals, using ceriu...
The regioselective introduction of a methoxymethyl (MOM) group on different type of glycols via an o...
The electrophilicity of the carbonyl group is a dominant feature of its extensive chemistry. A major...
Ytterbium triflate catalyses the deprotection of tert-butyl esters selectively in the presence of ot...
Ytterbium triflate catalyses the deprotection of tert-butyl esters selectively in the presence of ot...
A simple, mild and efficient method for deprotection of acetonides in the presence of molecular iodi...
813-814Trimethylsilyl ethers are selectively and rapidly oxidized to the corresponding carbonyl comp...
A variety of thioacetals and dithianes are deprotected into their carbonyl compounds in mild conditi...
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