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Title:	Intramolecular SN2 reaction at α-carbon of trifluoromethyl group: preparation of optically active 2-trifluoromethylaziridine
Source:	Tetrahedron: asymmetry [0957-4166] Katagiri, Toshimasa yr:1997

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description	1.	Osborn, Helen I. "The asymmetric synthesis of aziridines." Tetrahedron, asymmetry 8.11 (1997): 1693-1715.
description	2.	Lanier, M. "Nucleophilic ring opening of 3-F-alkyl 2,3-epoxypropanoates. Access to Î±,Î²-difunctional Î²-F-alkylpropanoates." Tetrahedron 52.46 (1996): 14631-14640.
description	3.	Ojima, I. "Synthesis of novel 3'-trifluoromethyl taxoids through effective kinetic resolution of racemic 4-CF3-beta-lactams with baccatins." Chirality 9.5-6 (1997): 487-494.
description	4.	Karimova, N. "Unusual reaction of trifluoroacetone with benzenesulfenyl chloride." Russian chemical bulletin 46.4 (1997).
description	5.	Rinaudo, G. "Synthesis of fluorinated Î±,Î²-diamino esters by ring opening of activated 3-trifluoromethyl-aziridine-2-carboxylates." Tetrahedron letters 47.13 (2006): 2065-2068.
description	6.	Sweeney, J B. "Aziridines: epoxides' ugly cousins?" Chemical Society reviews 31.5 (2002): 247-258.
description	7.	Hu, X. E. "Nucleophilic ring opening of aziridines." Tetrahedron 60.12 (2004): 2701-2743.
description	8.	McCoull, W. "Recent synthetic applications of chiral aziridines." Synthesis 2000.10 (2000): 1347-1365.
description	9.	Arnone, A. "Microbial reduction of Î±,Î±,Î±-trifluoro-Î±'-sulfenylketones." Tetrahedron letters 37.22 (1996): 3903-3906.
description	10.	Kim, Y. "Ring opening of 2-acylaziridines by acid chlorides." Tetrahedron 62.37 (2006): 8844-8849.
description	11.	Yamauchi, Y. "Generation and reactions of Î±-trifluoromethyl stabilized aziridinyl anion, a general synthetic precursor for stereospecific construction of Î±-amino-Î±-trifluoromethylated quaternary carbon." Tetrahedron letters 44.33 (2003): 6319-6322.
description	12.	Volonterio, A. "The "Non-Oxidative" Chloro-Pummerer Reaction: Novel stereospecific entry to vicinal chloroamines and aziridines." European journal of organic chemistry 19 (2002): 3336-3340.
description	13.	Abouabdellah, A. "Diastereoselective Synthesis of the Nonracemic Methyl syn-(3-Fluoroalkyl)isoserinates." Journal of organic chemistry 62.25 (1997): 8826-8833.
description	14.	Colantoni, D. "Unexpected and expeditious entry into trifluoromethyl aziridines from substituted beta-dicarbonyl compounds." Journal of organic chemistry 70.23 (2005): 9648-9650.
description	15.	COREY, E. "AN ENANTIOSELECTIVE SYNTHESIS OF (2S,3S)-3-HYDROXYLEUCINE AND (2R,3S)-3-HYDROXYLEUCINE." Tetrahedron Letters 33.45 (1992): 6735-6738.
description	16.	Cardillo, G. "Aziridines and oxazolines: Valuable intermediates in the synthesis of unusual amino acids." Aldrichimica acta 36.2 (2003): 39-50.
description	17.	Kim, Y. "Preparation of 2,3-diaminopropionate from ring opening of aziridine-2-carboxylate." Tetrahedron Letters 46.25 (2005): 4407-4409.
description	18.	Rayner, Christopher M. "Lewis acid-induced rearrangement of 1-hetero 2,3-epoxides. Synthesis, reactivity, and synthetic applications of homochiral thiiranium and aziridinium ion intermediates." Synlett 1 (1997): 11-.
description	19.	Watson, Iain G. "Advances in nitrogen transfer reactions involving aziridines." Accounts of chemical research 39.3 (2006): 194-206.
description	20.	Kolb, Hartmuth C. "Click chemistry: diverse chemical function from a few good reactions." Angewandte Chemie (International ed.) 40.11 (2001): 2004-2021.