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(b) Tanner, D. Chiral aziridines-Their synthesis and use in stereoselective transformations. Angew. Chem. Int. Ed. Engl. 1994, 33, 599-619;
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(c) Osborn, H. M. I.; Sweeney, J. The asymmetric synthesis of aziridines. Tetrahedron: Asymmetry 1997, 8, 1693-1715.
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Studies on the reaction of aziridines with nitriles and carbonyls: Synthesis of imidazolines and oxazolidines
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Gandhi, S.; Bisai, A.; Prasad, B. A. B.; Singh, V. K. Studies on the reaction of aziridines with nitriles and carbonyls: synthesis of imidazolines and oxazolidines. J. Org. Chem. 2007, 72, 2133-2142.
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(a) Rinaudo, G.; Narizuka, S.; Askari, N.; Crousse, B.; Bonnet-Delpon, D. Synthesis of fluorinated α,β-diamino esters by ring opening of activated 3-trifluoromethyl-aziridine-2-carboxylates. Tetrahedron Lett. 2006, 47, 2065-2068;
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(b) Bisai, A.; Pandey, M. K.; Singh, V. K. Regioselective ring opening of aziridines with activated DMF complexes: a facile synthesis of β-haloamines. Tetrahedron Lett. 2004, 45, 9661-9663;
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(c) Fan, R.-H.; Hou, X.-L. Efficient ring-opening reaction of epoxides and aziridines promoted by tributylphosphine in water. J. Org. Chem. 2003, 68, 726-730;
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Studies on ring cleavage of aziridines with hydroxyl compounds
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(d) Prasad, B. A. B.; Sanghi, R.; Singh, V. K. Studies on ring cleavage of aziridines with hydroxyl compounds. Tetrahedron 2002, 58, 7355-7363;
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An efficient method for the cleavage of aziridines using hydroxyl compounds
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(e) Prasad, B. A. B.; Sekar, G.; Singh, V. K. An efficient method for the cleavage of aziridines using hydroxyl compounds. Tetrahedron Lett. 2000, 41, 4677-4679;
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Efficient method for cleavage of aziridines with aromatic amines
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(f) Sekar, G.; Singh, V. K. Efficient method for cleavage of aziridines with aromatic amines. J. Org. Chem. 1999, 64, 2537-2539.
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Singh, V.K.2
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(a) Watson, I. D. G.; Yudin, A. K. Ring-opening reactions of nonactivated aziridines catalyzed by tris(pentafluorophenyl)borane. J. Org. Chem. 2003, 68, 5160-5167;
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(b) Riego, E.; Concellon, J. M. Ring opening of nonactivated 2-(1-aminoalkyl) aziridines: unusual regio- and stereoselective C-2 and C-3 cleavage. J. Org. Chem. 2003, 68, 6407-6410;
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Concellon, J.M.2
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Silica gel induced cleavage of aziridines by aromatic amines under solvent free conditions
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(c) Anand, R. V.; Pandey, G.; Singh, V. K. Silica gel induced cleavage of aziridines by aromatic amines under solvent free conditions. Tetrahedron Lett. 2002, 43, 3975-3976;
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An efficient method for opening nonactivated aziridines with TMS azide: Application in the synthesis of chiral 1,2-diaminocyclohexane
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(d) Chandrasekhar, M.; Sekar, G.; Singh, V. K. An efficient method for opening nonactivated aziridines with TMS azide: application in the synthesis of chiral 1,2-diaminocyclohexane. Tetrahedron Lett. 2000, 41, 10079-10083.
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Yadav, J. S.; Reddy, B. V. S.; Sadashiv, K.; Harikishan, K. Indium triflate-catalyzed ring opening of aziridines with carboxylic acids. Tetrahedron Lett. 2002, 43, 2099-2101.
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For reviews, see a, 2nd Edn, Beller, M. and Bolm, C. Eds, Wiley-VCH: Weinheim, Germany
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For reviews, see (a) Bolm, C.; Hildebrand, J. P.; Muniz, K. In Transition Metals for Organic Synthesis, 2nd Edn.; Beller, M. and Bolm, C. Eds.; Wiley-VCH: Weinheim, Germany, 2004, pp. 399-420;
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(b) Bergmeier, S. C. The synthesis of vicinal amino alcohols. Tetrahedron 2000, 56, 2561-2576;
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Reduction of carbonyl compounds with chiral oxazaborolidine catalysts: A new paradigm for enantioselective catalysis and a powerful new synthetic method
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(c) Corey, E. J.; Helal, C. J. Reduction of carbonyl compounds with chiral oxazaborolidine catalysts: a new paradigm for enantioselective catalysis and a powerful new synthetic method. Angew. Chem., Int. Ed. 1998, 37, 1986-2012;
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Helal, C.J.2
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(d) Ager, J. D.; Prakash, I.; Schaad, D. R. 1,2-Amino alcohols and their heterocyclic derivatives as chiral auxiliaries in asymmetric synthesis. Chem. Rev. 1996, 96, 835-875.
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A convenient method for obtaining trans-2-aminocyclohexanol and trans-2-aminocyclopentanol in enantiomerically pure form
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Overman, L. E.; Sugai, S. A convenient method for obtaining trans-2-aminocyclohexanol and trans-2-aminocyclopentanol in enantiomerically pure form. J. Org. Chem. 1985, 50, 4154-4155.
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Schiffers, I.; Rantanen, T.; Schmidt, F.; Bergmans, W.; Zani, L.; Bolm, C. Resolution of racemic 2-aminocyclohexanol derivatives and their application as ligands in asymmetric catalysis. J. Org. Chem. 2006, 71, 2320-2331.
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