Organic Chemistry Portal

Abstracts

Search:



Reactivity and selectivity in Lewis acid-catalyzed Diels-Alder reactions of 2-cyclohexenones.

F. Fringuelli, L. Minuti, F. Pizzo, A. Taticchi, Acta Chem. Scand., 1993, 47, 255.

Key Words:



F. Fringuelli, O. Piermatti, F. Pizzo, in Targets in Heterocyclic Systems, Vol. 1 (Eds.: O. A. Attanasi, D. Spinelli), Italian Society Chemistry, Viale Liegi/ 48/00198 Rome/Italy, 1997, pp. 57.

Key Words:



F. Fringuelli, O. Piermatti, F. Pizzo, in Recent Research Developments in Organic Chemistry, Vol. 1 (Ed.: S. G. Pandalai), Transworld Research Network, Tc 36/248 1/Trivandrum 695008/India, 1997, pp. 123.

Key Words:



F. Fringuelli, O. Piermatti, F. Pizzo, in Trends in Organic Chemistry, Vol. 6 (Eds.: P. A. Aristoff, W. G. Bentrude, W. T. Borden, S. D. Burke, D. P. Curran, R. L. Danheiser, S. J. Danishefsky, B. Giese, S. Hanessian), Research Trends, T C 17/250 (3)/Chadiyara Rd, Poojapura/Trivandrum 695012/India, 1997, pp. 181.

Key Words:



Synthesis and reactivity of pyronoids in aqueous medium.

F. Fringuelli, O. Piermatti, F. Pizzo, Heterocycles, 1999, 50, 611.

Key Words:
DIELS-ALDER REACTION/ONE-POT SYNTHESIS/ORGANIC-REACTIONS/WATER/COUMARINS/CATALYSTS/DIENE/2'-HYDROXYCHALCONES/CHEMISTRY/FLAVONES



Recent advances in Lewis acid catalyzed Diels-Alder reactions in aqueous media.

F. Fringuelli, O. Piermatti, F. Pizzo, L. Vaccaro, Eur. J. Org. Chem., 2001, 439.

Key Words:
cycloadditions; Diels-Alder reaction; green chemistry; Lewis acids; WATER-ENHANCED ENANTIOSELECTIVITY; MOLECULAR-ORBITAL INTERACTION; HAMMETT REACTION CONSTANT; HOST-GUEST CHEMISTRY; ORGANIC-SYNTHESIS; ASYMMETRIC-SYNTHESIS; MICELLAR CATALYSIS; ORGANOMETALLIC CHEMISTRY; MONOPEROXYPHTHALIC ACID; HOMOGENEOUS CATALYSIS



F. Fringuelli, A. Taticchi, Dienes in the Diels-Alder Reaction., Wiley, New York, 1990.

Key Words:



Diels-Alder reactions of cycloalkenones in organic synthesis. A review.

F. Fringuelli, A. Taticchi, E. Wenkert, Org. Prep. Proced. Int., 1990, 22, 131.

Key Words:
C-C BOND FORMATION/PERICYCLIC REACTIONS/CYCLOADDITIONS/[4+2]/CARBRING/6