Heterocyclic tricycles as internal N-glycosides from 2-methyl-5-nitro-6-(2-nitrophenyl)-4-phenyl(2-furyl) tetrahydropyranols

Citation
L. Gotze et al., Heterocyclic tricycles as internal N-glycosides from 2-methyl-5-nitro-6-(2-nitrophenyl)-4-phenyl(2-furyl) tetrahydropyranols, MOLECULES, 5(3), 2000, pp. 245-251
Citations number
6
Categorie Soggetti
Organic Chemistry/Polymer Science
Journal title
MOLECULES
ISSN journal
14203049 → ACNP
Volume
5
Issue
3
Year of publication
2000
Pages
245 - 251
Database
ISI
SICI code
1420-3049(200003)5:3<245:HTAINF>2.0.ZU;2-7
Abstract
1-Methyl-10-nitro-11-phenyl(2-furyl)-2-aza-13-oxa-tricyclo[7.3.1.0(3,8)]tri deca-3,5,7- trienes 3 were synthesized via the reduction of the aromatic 2- nitro group of 2-methyl-5-nitro-6-(2-nitrophenyl) -4-phenyl(2-furyl)tetrahy dropyranols 2 and subsequent condensation with their anomeric OH group. As by-products, the corresponding 6-(2-aminophenyl)-2-methyl-5-nitro-4-phenyl( 2-furyl)tetrahydropyranols 4 were isolated.