Metal catalyzed 1,3-dipolar cycloaddition reaction of azomethine ylides enantioselective synthesis of heteroaryl substituted prrolidines

2018-09-05

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Metal catalyzed asymmetric synthesis of thienyl-substituted pyrrolidines by 1,3-dipolar cycloaddition reaction of azomethine ylides
Bulut, Merve; Doğan, Özdemir; Department of Chemistry (2019)
Pyrrolidines are structurally and biologically important heterocyclic compounds. One of the efficient methods for the synthesis of these compounds is 1,3-dipolar cycloaddition (1,3-DC) reaction of azomethine ylides with electron deficient dipolarophiles. Asymmetric synthesis of these compounds has been studied by many groups by using 1,3-DC reactions with chiral transition metal catalysts. In all these studies aryl-substituted pyrrolidines were synthesized mainly. In this thesis, heteroaryl-substituted pyrr...
Metal catalyzed asymmetric synthesis of heteroaryl substitıted pyrolidines
Doğan, Özdemir; Gözükara, Zeynep; Araz, Mihrimah; Polat Çakır, Sıdıka (null; 2019-10-15)
METAL CATALYZED ASYMMETRIC SYNTHESIS OF HETEROARYL SUBSTITUTED PYRROLIDINES
Doğan, Özdemir; Gözükara, Zeynep; Aras, Mihrimah; Polat Çakır, Sıdıka (null; 2019-09-21)
Metal catalyzed and organocatalytic asymmetric synthesis
Doğan, Özdemir (null; 2015-09-07)
Metal triflates-catalyzed conjugate addition of homochiral Pyrroles to alpha,beta-unsaturated esters
Unaleroglu, C; Temelli, B; Demir, Ayhan Sıtkı (Georg Thieme Verlag KG, 2004-10-18)
The Friedel-Crafts reaction of homochiral pyrrole derivatives with alpha,beta-unsaturated esters catalyzed by metal triflates furnished conjugate addition products. The best yields were obtained by using yttrium triflate and methyl 4-phenyl-2-oxobut-3-enoate (2a). The addition worked regioselectively at C-5 of pyrrole. The diastereoisomers were separated by column chromatography.
Citation Formats
Ö. Doğan, “Metal catalyzed 1,3-dipolar cycloaddition reaction of azomethine ylides enantioselective synthesis of heteroaryl substituted prrolidines,” 2018, Accessed: 00, 2021. [Online]. Available: https://hdl.handle.net/11511/79232.