REGIOSELECTIVITY AND STEREOSELECTIVITY IN 1,3-DIPOLAR CYCLOADDITION REACTIONS OF 1-(PHTHALAZIN-1-YL)PYRIDINIUM-3-OLATE WITH 2-PI-1,3-DIPOLAROPHILES

Citation
Sa. Elabbady et Ah. Moustafa, REGIOSELECTIVITY AND STEREOSELECTIVITY IN 1,3-DIPOLAR CYCLOADDITION REACTIONS OF 1-(PHTHALAZIN-1-YL)PYRIDINIUM-3-OLATE WITH 2-PI-1,3-DIPOLAROPHILES, Journal of chemical research. Synopses, (7), 1995, pp. 298
Citations number
15
Categorie Soggetti
Chemistry
ISSN journal
03082342
Issue
7
Year of publication
1995
Database
ISI
SICI code
0308-2342(1995):7<298:RASI1C>2.0.ZU;2-X
Abstract
Cycloaddition to 1-(phthalazin-1-yl)pyridinium-3-olate across the 2,6- positions of the pyridine ring with 2 pi-electron addends gives substi tuted 8-azabicyclo[3.2.1]oct-3-en-2-ones, the structural and configura tional assignments of which have been deduced from H-1 NMR and IR spec tral data.