f-shirini documents

ChemInform Abstract: Polymer Supported Reagents: Oxidative Selection Between Benzylic Alcohols
Documents ChemInform Abstract: Polymer Supported Reagents: Oxidative Selection Between Benzylic Alcohols
ChemInform Abstract: [(NO3)3Ce] 3×H2IO6: As a Versatile and Efficient Reagent for Cleavage of Carbon—Nitrogen Double Bonds under Heterogeneous and Non-aqueous Conditions
Documents ChemInform Abstract: [(NO3)3Ce] 3×H2IO6: As a Versatile and Efficient Reagent for Cleavage of Carbon—Nitrogen Double Bonds under Heterogeneous and Non-aqueous Conditions
ChemInform Abstract: A Mild and Efficient Method for Cleavage of C=N Using Mg(HSO4)2 in the Presence of Wet SiO2
Documents ChemInform Abstract: A Mild and Efficient Method for Cleavage of C=N Using Mg(HSO4)2 in the Presence of Wet SiO2
ChemInform Abstract: Oxidation of Alcohols by (NH4)2Cr2O7 in Solution and under Solvent-Free Conditions
Documents ChemInform Abstract: Oxidation of Alcohols by (NH4)2Cr2O7 in Solution and under Solvent-Free Conditions
ChemInform Abstract: Efficient Oxidation of Sulfides to Sulfoxides and of Thiols to Disulfides with Aqueous HIO3
Documents ChemInform Abstract: Efficient Oxidation of Sulfides to Sulfoxides and of Thiols to Disulfides with Aqueous HIO3
ChemInform Abstract: Efficient Solvent Free Deoximation and Dehydrazonation with HIO3 in the Presence of Wet SiO2
Documents ChemInform Abstract: Efficient Solvent Free Deoximation and Dehydrazonation with HIO3 in the Presence of Wet SiO2
ChemInform Abstract: Oxidation of Benzyl Alcohols under Mild Heterogeneous Conditions
Documents ChemInform Abstract: Oxidation of Benzyl Alcohols under Mild Heterogeneous Conditions
Efficient Cleavage of Carbon—Nitrogen Double Bonds under Solvent-Free Conditions
Documents Efficient Cleavage of Carbon—Nitrogen Double Bonds under Solvent-Free Conditions
Polymer Supported Reagents: Oxidative Selection Between Thiols
Documents Polymer Supported Reagents: Oxidative Selection Between Thiols
Oxidation of Alcohols Using (NH4)2Cr2O7 in the Presence of Silica Chloride/Wet SiO2 in Solution and under Solvent-Free Conditions
Documents Oxidation of Alcohols Using (NH4)2Cr2O7 in the Presence of Silica Chloride/Wet SiO2 in Solution and under Solvent-Free Conditions
Regeneration of Carbonyl Compounds by Cleavage of C=N Bonds under Mild and Completely Heterogeneous Conditions
Documents Regeneration of Carbonyl Compounds by Cleavage of C=N Bonds under Mild and Completely Heterogeneous Conditions
Al(HSO4)3 Catalyzed Acetylation and Formylation of Alcohols
Documents Al(HSO4)3 Catalyzed Acetylation and Formylation of Alcohols
Chemoselective Solvent-Free Deoximation by (NH4)2Cr2O7 in the Presence of ZrCl4 on Wet SiO2
Documents Chemoselective Solvent-Free Deoximation by (NH4)2Cr2O7 in the Presence of ZrCl4 on Wet SiO2
A Mild and Efficient Method for the Acetylation of Alcohols
Documents A Mild and Efficient Method for the Acetylation of Alcohols
Mild and Efficient Procedure for Acetylation and Formylation of Alcohols in the Presence of Mg(HSO4)2
Documents Mild and Efficient Procedure for Acetylation and Formylation of Alcohols in the Presence of Mg(HSO4)2
Polymer-Supported Reagents. Mild and Efficient Method of Oxidation of Alcohols
Documents Polymer-Supported Reagents. Mild and Efficient Method of Oxidation of Alcohols
CaCl2×2H2O Assisted Oxidation of Alcohols with (NH4)2Cr2O7
Documents CaCl2×2H2O Assisted Oxidation of Alcohols with (NH4)2Cr2O7
Selective Oxidative Deprotection of Trimethylsilyl Ethers in Solution and under a Solvent-Free Condition
Documents Selective Oxidative Deprotection of Trimethylsilyl Ethers in Solution and under a Solvent-Free Condition
[Ce(NO3)3] 3×H2IO6: Efficient Oxidation Reactions under Solvent-Free Conditions
Documents [Ce(NO3)3] 3×H2IO6: Efficient Oxidation Reactions under Solvent-Free Conditions
ChemInform Abstract: An Efficient and Chemoselective Method for Synthesis of 1,3-Oxathiolanes from Aldehydes and Their Deprotection Catalyzed by V(HSO4)3
Documents ChemInform Abstract: An Efficient and Chemoselective Method for Synthesis of 1,3-Oxathiolanes from Aldehydes and Their Deprotection Catalyzed by V(HSO4)3
ChemInform Abstract: Melamine Trisulfonic Acid as a New, Efficient and Reusable Catalyst for the Chemoselective Oxathioacetalization of Aldehydes
Documents ChemInform Abstract: Melamine Trisulfonic Acid as a New, Efficient and Reusable Catalyst for the Chemoselective Oxathioacetalization of Aldehydes