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Synthesis, Characterization and Properties of a Series of Copoly(amide-imide-ether-urethane)s with a New Hard Segment Constituent. Study of the Effect of Hard Segment Content
Microwave heating in combination with ionic liquids: synthesis and properties of novel optically active polyamides, thermal degradation and electrochemical stability on multi-walled carbon nanotubes electrode
Microwave-Accelerated Preparation of Aromatic Polyamides Containing Phthalimide and S-Valine Pendent Groups in Ionic Liquids
23. Preparation of new optically active polyamides containing L-phenylalanine, phthalimide side chain via diisocyanate route by microwave energy: Comparison with conventional heating
Application of Microwave-assisted Reactions in Step-Growth Polymerization (A Review).
Use of ionic liquid and microwave irradiation as a convenient, rapid and eco-friendly method for synthesis of novel optically active and highly organosoluble aromatic polyamides containing N-phthaloyl-L-alanine pendent group
Safe and fast polyamidation of 5-[4-(2-phthalimidiyl-propanoylamino)benzoylamino]-isophthalic acid with aromatic diamines in ionic liquid under microwave irradiation
A facile, microwave-assisted synthesis of novel optically active polyamides derived from 3-methyl-2-(phthalimidylpentanoyl-amino)isophthalic acid and different diisocyanates
One-pot polyamidation reaction of optically active aromatic diacid containing methionine and phthalimide moieties with aromatic diamines under microwave irradiation and traditional heating
Benzyltriphenylphosphonium Peroxymonosulfate: As a Novel and Efficient Reagent for Oxidation of Alcohols under Solvent-Free Conditions
An Efficient, Fast and Selective Oxidation of Aliphatic and Benzylic Alcohols to the Corresponding Carbonyl Compounds under Microwave Irradiation.
An Efficient, Fast and Selective Oxidation of Aliphatic and Benzylic Alcohols to the Corresponding Carbonyl Compounds under Microwave Irradiation.
Benzyltriphenylphosphonium Dichromate as a Mild Reagent for Oxidation of Thiol and Sulfides.
Oxidation of Urazoles to their Corresponding Triazolinediones Under Mild and Heterogeneous Conditions.
OXIDATION OF URAZOLES TO THEIR CORRESPONDING TRIAZOLINEDIONES UNDER MILD AND HETEROGENEOUS CONDITIONS VIA IN SITU GENERATION OF NOIOX