1. Reviews on 1,2,3-triazoles, see: (a) Dehne, H. In Methoden der Organischen Chemie (Houben–Weyl); Schumann, E., Ed.; Thieme: Stuttgart, 1994; Vol. E8d, pp. 305–405; (b) Wamhoff, H. In Comprehensive Heterocyclic Chemistry; Katritzky, A. R.; Rees, C. W., Eds.; Pergamon: Oxford, 1984; Vol. 5, pp. 669–732; (c) Sheradsky, T. In The Chemistry of the Azido Group; Patai, S., Ed.; Interscience: London, 1971; pp. 377–382; (d) Abu-Orabi, S. T.; Atfah, M. A.; Jibril, I.; Mari'i, F. M.; Ali, A. A.-S. J. Heterocyclic. Chem. 1989, 26, 1461–1468.
2. Studies on v-triazoles. Part 4. The 4-methoxybenzyl group, a versatile N-protecting group for the synthesis of N-unsubstituted v-triazoles
3. Studies on v-triazoles. 7. Antiallergic 9-oxo-1H,9H-benzopyrano[2,3-d]-v-triazoles
4. Studies on 1,2,3-triazoles. 13. (Piperazinylalkoxy)-[1]benzopyrano[2,3-d]-1,2,3-triazol-9(1H)-ones with combined H1-antihistamine and mast cell stabilizing properties
5. 1,2,3-Triazole-[2,5-Bis-O-(tert-butyldimethylsilyl)-.beta.-D-ribofuranosyl]-3'-spiro-5''-(4''-amino-1'',2''-oxathiole 2'',2''-dioxide) (TSAO) Analogs: Synthesis and Anti-HIV-1 Activity