Add to ORKG1145-1150Microwave assisted N-O bond cleavage of novel N-methyl isoxazolidines under mild conditions have been studied and found to afford 1,3-amino alcohols readily with high yield in a short reaction time
In this paper, the microwave (MW)-assisted catalyst-free and mostly solvent-free Kabachnik−Fie...
Organic Chemistry Laboratory, Sikkim Government College, Gangtok-737 102, Sikkim, India E-mail : bc...
An expedient intramolecular olefin–nitrone cycloaddition (INC) route is reported for the synthesis o...
ß-amino alcohols are common substructures in many biologically active compounds and can also be used...
Copyright © 2014 Adrián Ochoa-Terán et al. This is an open access article distributed under the Cr...
A simple and efficient microwave-assisted methodology for the synthesis of 4-substituted-3-methyl-1,...
1784-1786Trimolecular condensation of N-(5-methyl-3- isoxazolyl)- N'-aryl ureas 2 with aqueous for...
A general and efficient method has been developed for the alcoholysis of isocyanates derived from th...
In an attempt to form 2-alkylidene-1,3-oxazolidines, chiral 2-oxazolines have been N-alkylated and N...
A simple and efficient protocol has been developed for the direct synthesis of γ-nitrobutyric acid m...
Ring cleavage of a variety of N-substituted aziridines has been studied with hydroxyl compounds (pri...
Aminolysis of eposides with ammonium acetate has been achieved for the first time under microwave ir...
Background: Aminoisoquinolines are an important class of heterocyclic compounds. These compounds pre...
1509-1513Synthesis of few new scaffolds for isoxazolidine derivatives have been reported from amino ...
A number of oxazolidines derived from ketones and aminoalcohols have been prepared in excellent yiel...
In this paper, the microwave (MW)-assisted catalyst-free and mostly solvent-free Kabachnik−Fie...
Organic Chemistry Laboratory, Sikkim Government College, Gangtok-737 102, Sikkim, India E-mail : bc...
An expedient intramolecular olefin–nitrone cycloaddition (INC) route is reported for the synthesis o...
ß-amino alcohols are common substructures in many biologically active compounds and can also be used...
Copyright © 2014 Adrián Ochoa-Terán et al. This is an open access article distributed under the Cr...
A simple and efficient microwave-assisted methodology for the synthesis of 4-substituted-3-methyl-1,...
1784-1786Trimolecular condensation of N-(5-methyl-3- isoxazolyl)- N'-aryl ureas 2 with aqueous for...
A general and efficient method has been developed for the alcoholysis of isocyanates derived from th...
In an attempt to form 2-alkylidene-1,3-oxazolidines, chiral 2-oxazolines have been N-alkylated and N...
A simple and efficient protocol has been developed for the direct synthesis of γ-nitrobutyric acid m...
Ring cleavage of a variety of N-substituted aziridines has been studied with hydroxyl compounds (pri...
Aminolysis of eposides with ammonium acetate has been achieved for the first time under microwave ir...
Background: Aminoisoquinolines are an important class of heterocyclic compounds. These compounds pre...
1509-1513Synthesis of few new scaffolds for isoxazolidine derivatives have been reported from amino ...
A number of oxazolidines derived from ketones and aminoalcohols have been prepared in excellent yiel...
In this paper, the microwave (MW)-assisted catalyst-free and mostly solvent-free Kabachnik−Fie...
Organic Chemistry Laboratory, Sikkim Government College, Gangtok-737 102, Sikkim, India E-mail : bc...
An expedient intramolecular olefin–nitrone cycloaddition (INC) route is reported for the synthesis o...