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AN EASY AND EFFICIENT METHOD FOR OXIDATION OF ALCOHOLS AND AROMATIC AMINES TO THE CORRESPONDING CARBONYL AND AZO COMPOUNDS UNDER NON-AQUEOUS AND NEUTRAL CONDITIONS
Application of New Objective Function To Improve Models of Structures under Dynamic Environment
1-BENZYL-1-AZA-4-AZONIABICYCLO 2.2.2 -OCTANE PERIODATE AS NEW OXIDANT FOR OXIDATION OF THIOLS AND SULFIDES TO THE CORRESPONDING DISULFIDES AND SULFOXIDES UNDER ANHYDROUS CONDITIONS
AN EASY AND EFFICIENT METHOD FOR CLEAVAGE OF CARBON-NITROGEN DOUBLE BONDS UNDER NON-AQUEOUS AND NEUT
BENZYLTRIPHENYLPHOSPHONIUM PEROXODISULFATE (PHCH2PPH3)(2)S2O8 A MILD AND INEXPENSIVE REAGENT FOR EFFICIENT OXIDATION OF ORGANIC COMPOUNDS UNDER NONAQUEOUS AND APROTIC CONDITIONS
BIS(1-BENZYL-4-AZA-1-AZONIABICYCLO 2.2.2 OCTANE) PEROXODISULFATE A MILD AND EFFICIENT OXIDANT FOR CLEAVAGE OF NITROGEN DOUBLE BONDS AND OXIDATION OF ALCOHOLS UNDER ANHYDROUS CONDITIONS
1-BENZYL-4-AZA-1-AZONIABICYCLO 2.2.2 OCTANE PERIODATE A MILD AND EFFICIENT OXIDANT FOR THE CLEAVAGE OF OXIME DOUBLE BONDS UNDER ANHYDROUS CONDITIONS
Dynamic Response of Adjacent Structures Under Spatially Deterministic and Random Propagation of Seismic Waves
A FACILE AND EFFICIENT METHOD FOR THE REGENERATION OF CARBONYL COMPOUNDS FROM HYDRAZONES AND OXIMES BY OXONE (R) UNDER HETEROGENEOUS CONDITIONS
OXIDATION OF ALCOHOLS TO CARBONYL COMPOUNDS UNDER SOLVENT-FREE CONDITIONS USING PERMANGANATE SUPPORTED ON ALUMINA
BIS(1-BENZYL-4-AZA-1-AZONIABICYCLO 2.2.2 OCTANE) PEROXODISULFATE A MILD AND EFFICIENT OXIDANT FOR CLEAVAGE OF OXIME DOUBLE BONDS UNDER ANHYDROUS CONDITIONS
A CONVENIENT AND MILD PROCEDURE FOR THE SYNTHESIS OF ALKYL P-TOLUENESULFINATES UNDER SOLVENT-FREE CONDITIONS USING MICROWAVE IRRADIATION
A RAPID AND CONVENIENT SYNTHESIS OF OXIMES IN DRY MEDIA UNDER MICROWAVE IRRADIATION
A CONVENIENT AND HIGHLY DIASTEREOSELECTIVE SYNTHESIS OF OPTICALLY ACTIVE SULFINATE ESTERS FROM SULFONYL CHLORIDES UNDER SOLID STATE CONDITIONS
A CONVENIENT AND MILD PROCEDURE FOR THE SYNTHESIS OF HYDRAZONES AND SEMICARBAZONES FROM ALDEHYDES OR KETONES UNDER SOLVENT-FREE CONDITIONS
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