An efficient selective deprotection followed by acetylation of several benzyl ethers, including 6-OBn ethers of monosaccharides, and -OTBDMS ethers has been developed by using the BF<SUB>3</SUB>·Et<SUB>2</SUB>O-NaI-Ac<SUB>2</SUB>O reagent system. In addition, both benzylidene and isopropylidene groups are deprotected to form the corresponding diacetates
Benzyltriethylammonium tetrathiomolybdate, [PhCH2NEt3](2)MoS4, 1 deprotects propargyl ethers of alco...
Carbamate-bearing benzylated aminosugars undergo an I2/I(III)-promoted intramolecular hydrogen atom ...
Protecting groups are indispensable in organic synthesis and there is a great need for a variety of ...
863-8641,1-Diacetates are efficiently deprotected by using CeCl3.7H2O-Nal system affording the alde...
Catalytic amounts of bromodimethyl sulfonium bromide, or Nafion-H along with NaI (1 equiv.), in meth...
Department of Organic Chemistry, Indian Association for the Cultivation of Science, Calcutta-700 032...
The reactivity order of O-deisopropylidenation of the three isopropylidene protecting groups of 2',6...
An efficient and convenient method for the removal of benzyl ether protecting groups in the presence...
An efficient and convenient method for the removal of benzyl ether protecting groups in the presence...
A reliable reagent system for the cleavage of 4-(3,4-dimethoxyphenyl)benzyl (DMPBn) ethers under ac...
1251-12561-Benzyl-4-aza-1-azoniabicyclo[2.2.2]octane dichromate (BAABOD) is a useful reagent for th...
Abstract—A new efficient method for deprotection of TBDMS derivatives of phenols, primary alcohols, ...
A new procedure for the deprotection of carboxylic tert-butyl and 1-adamantyl esters, and N-Boc-amin...
A highly efficient and mild method for the de-O-benzylation of protected saccharides was developed b...
Benzyltriethylammonium tetrathiomolybdate, [PhCH2NEt3](2)MoS4, 1 deprotects propargyl ethers of alco...
Benzyltriethylammonium tetrathiomolybdate, [PhCH2NEt3](2)MoS4, 1 deprotects propargyl ethers of alco...
Carbamate-bearing benzylated aminosugars undergo an I2/I(III)-promoted intramolecular hydrogen atom ...
Protecting groups are indispensable in organic synthesis and there is a great need for a variety of ...
863-8641,1-Diacetates are efficiently deprotected by using CeCl3.7H2O-Nal system affording the alde...
Catalytic amounts of bromodimethyl sulfonium bromide, or Nafion-H along with NaI (1 equiv.), in meth...
Department of Organic Chemistry, Indian Association for the Cultivation of Science, Calcutta-700 032...
The reactivity order of O-deisopropylidenation of the three isopropylidene protecting groups of 2',6...
An efficient and convenient method for the removal of benzyl ether protecting groups in the presence...
An efficient and convenient method for the removal of benzyl ether protecting groups in the presence...
A reliable reagent system for the cleavage of 4-(3,4-dimethoxyphenyl)benzyl (DMPBn) ethers under ac...
1251-12561-Benzyl-4-aza-1-azoniabicyclo[2.2.2]octane dichromate (BAABOD) is a useful reagent for th...
Abstract—A new efficient method for deprotection of TBDMS derivatives of phenols, primary alcohols, ...
A new procedure for the deprotection of carboxylic tert-butyl and 1-adamantyl esters, and N-Boc-amin...
A highly efficient and mild method for the de-O-benzylation of protected saccharides was developed b...
Benzyltriethylammonium tetrathiomolybdate, [PhCH2NEt3](2)MoS4, 1 deprotects propargyl ethers of alco...
Benzyltriethylammonium tetrathiomolybdate, [PhCH2NEt3](2)MoS4, 1 deprotects propargyl ethers of alco...
Carbamate-bearing benzylated aminosugars undergo an I2/I(III)-promoted intramolecular hydrogen atom ...
Protecting groups are indispensable in organic synthesis and there is a great need for a variety of ...