1 O 2',3' DI PHENYL 5' METHYL ISOXAZOLIDIN 4' YL] 2,3,4 TRI O BENZOYL ALPHA XYLOPYRANOSE;
1 O 2',3' DI PHENYL 5' METHYL ISOXAZOLIDIN 4' YL] 2,3,4 TRI O BENZOYL BETA XYLOPYRANOSE;
1 O 2',3' DI PHENYL 5' METHYL ISOXAZOLIDIN 4' YL] 2,3,4,6 TETRA O ACETYL BETA GLUCOPYRANOSE;
CARBOHYDRATE DERIVATIVE;
METHYL 2,3,4 TRI O ACETYL 6 O 2',3' DI PHENYL 5' METHYL ISOXAZOLIDIN 4' YL]ALPHA GLUCOPYRANOSIDE;
UNCLASSIFIED DRUG;
Cycloadditions under microwave irradiation conditions: Methods and applications
de la Hoz, A.; Diaz-Ortis, A.; Moreno, A.; Langa, F. Cycloadditions under microwave irradiation conditions: Methods and applications. Eur. J. Org. Chem. 2000, 3659-3673.
R. M. Giuliano (Ed.); American Chemical Society: Washington, D.C.
Fisera, L.; Al-Timari, U. A. R.; Ertl, P. In Stereoselectivity of 1,3-Dipolar Cycloaddition of Glycosyl Nitrones To N-Arylmaleimides; R. M. Giuliano (Ed.); American Chemical Society: Washington, D.C., 1992; pp. 158-171.
[1,3]-Dipolar intramolecular nitrone olefin cycloaddition reaction of a sugar-derived a,b-unsaturated ester: A new diastereo-and regioselective synthesis of an aminocyclopentitol
Jachak, S. M.; Karche, N. P.; Dhavale, D. D. [1,3]-Dipolar intramolecular nitrone olefin cycloaddition reaction of a sugar-derived a,b-unsaturated ester: A new diastereo-and regioselective synthesis of an aminocyclopentitol. Tetrahedron Lett. 2001, 42, 4925-4928.
1,3-Dipolar cycloadditions in the synthesis of carbohydrate mimics, part 2: Nitrones and oximes
Koumbis, A. E.; Gallos, J. K. 1,3-Dipolar cycloadditions in the synthesis of carbohydrate mimics, part 2: Nitrones and oximes. Curr. Org. Chem. 2003, 7, 585-628.
Synthesis of novel carbohydrate acridinone derivatives with potential biological activities using 1,3-dipolar cycloaddition
Fascio, M. L.; D'Accorso, N. B.; Pellon, R. F.; Docampo, M. L. Synthesis of novel carbohydrate acridinone derivatives with potential biological activities using 1,3-dipolar cycloaddition. Synth. Commun. 2007, 37, 4209-4217.
1 3-Dipolar cycloaddition reactions on carbohydrate-based templates: Synthesis of spiro-isoxazolines and 1, 2,4-oxadiazoles as glycogen phosphorylase inhibitors
Benltifa, M.; Vidal, S.; Gueyrard, D.; Goekjian, P. G.; Msaddek, M.; Praly, J. P. 1,3-Dipolar cycloaddition reactions on carbohydrate-based templates: Synthesis of spiro-isoxazolines and 1,2,4-oxadiazoles as glycogen phosphorylase inhibitors. Tetrahedron Lett. 2006, 47, 6143-6147.
1,3-Dipolar cycloaddition reactions of carbohydrate derived nitrones and oximes
Osborn, H. M. I.; Gemmell, N.; Harwood, L. M. 1,3-Dipolar cycloaddition reactions of carbohydrate derived nitrones and oximes. J. Chem. Soc. Perk. Trans. 1 2002, 2419-2438.
Exploiting microwave-assisted neat procedures: Synthesis of N-aryl and N-alkylnitrones and their cycloaddition en route for isoxazolidines
Andrade, M. M.; Barros, M. T.; Pinto, R. C. Exploiting microwave-assisted neat procedures: Synthesis of N-aryl and N-alkylnitrones and their cycloaddition en route for isoxazolidines. Tetrahedron 2008, 64, 10521-10530.
Selective synthesis under microwave irradiation of carbohydrate derivatives containing unsaturated systems
Andrade, M. M.; Barros, M. T.; Rodrigues, P. Selective synthesis under microwave irradiation of carbohydrate derivatives containing unsaturated systems. Eur. J. Org. Chem. 2007, 3655-3668.
Exploiting microwave-assisted neat procedures: Synthesis of N-aryl and N-alkylnitrones and their cycloaddition en route for isoxazolidines
Andrade, M. M.; Barros, M. T.; Pinto, R. C. Exploiting microwave-assisted neat procedures: Synthesis of N-aryl and N-alkylnitrones and their cycloaddition en route for isoxazolidines. Tetrahedron 2008, 64, 10521-10530.