Enantioselective synthesis of 1, 2, 5, 6-tetrahydropyridines (THPs) via proline-catalyzed direct Mannich-cyclization/domino oxidation–reduction sequence: application for medicinally important N-heterocycles. Issue 65 (22nd June 2016)

• Record Type: Journal Article
• Authors: Ramaraju, Panduga; Mir, Nisar A.; Singh, Deepika; Kumar, Indresh
• Is Part Of: RSC advances. Volume 6:Issue 65(2016)
• Page Start: 60422
• Page End: 60432
• Publication Date: 2016-06-22
• Subjects: Chemistry -- Periodicals; 540.5
• DOI: 10.1039/c6ra12965j
• Languages: English
• ISSNs: 2046-2069

Abstract

Abstract : An enantioselective multi-component synthesis of 1, 2, 5, 6-tetrahydropyridines (THPs) has been developed through a one-pot domino-process. Abstract : An enantioselective multi-component synthesis of 1, 2, 5, 6-tetrahydropyridines (THPs) has been developed through a one-pot domino-process. This transformation proceeds through proline-catalyzed direct Mannich reaction-cyclization of glutaraldehyde with in situ generated imines, followed by site-selective oxidation–reduction sequence under mild conditions. Chiral 1, 2, 5, 6-THPs are obtained in good to high yields (up to 80%) and with the excellent enantioselectivity (up to 98 : 2 er). The usefulness of this operationally simple method is also shown to synthesize other medicinally important nitrogen-heterocycles.