An enantioselective route to pyrrolidines: Removal of the chiral template from homochiral pyrroloimidazoles
Author:
Publisher
Elsevier BV
Subject
Organic Chemistry,Drug Discovery,Biochemistry
Reference9 articles.
1. Jones, R.C.F.; Howard, K.J.; Snaith, J.S. preceding Letter.
2. Annulation of imidazolines: A 1,3-dipolar cycloaddition route to pyrroloimidazoles, pyrrolidines and pyrroles
3. 1,3-Dipolar cyctoadditions of 4,5-dihydroimidazolium ylides: new protocols for the synthesis of pyrrolidines and pyrrolo[1,2-a]pyrazines
4. A new reagent for the selective, high-yield N-dealkylation of tertiary amines: improved syntheses of naltrexone and nalbuphine
5. Tests of a piperidino mask for the protection of functionalized carbon sites in multistep syntheses
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2. DABCO-catalyzed [3 + 2] annulation of sulfamate-derived cyclic imines with isocyanoacetates: synthesis of sulfamate-fused 2-imidazoline;Organic & Biomolecular Chemistry;2014-06-26
3. One-step synthesis of imidazoline-containing macrocycles and their complexation with fullerenes C60 and C70;Chemical Communications;2013
4. Synthesis and Synthetic Applications of 1-Aryl-2-alkyl-4,5-dihydro-1H-imidazoles;Synthetic Communications;2012-07-15
5. An enantioselective route to pyrrolidines: removal of the chiral template from homochiral pyrroloimidazoles;Tetrahedron;2011-11
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