Diastereoselective synthesis of 1-α-phenylethyl-3,3-dimethyldiaziridine. Conformation and configuration of three-membered ring nitrogen heterocycles containing an asymmetric substituent on the nitrogen atom

[1]  D. Boyd,et al.  Dynamic stereochemistry of imines and derivatives. Part 16. Conformation and stereodynamics of oxaziridines, nitrones, and imines containing the N-(1-mesitylethyl) or (1-pentamethylphenylethyl) group; a nuclear magnetic resonance and X-ray crystallographic investigation , 1984 .

[2]  L. Atovmyan,et al.  Asymmetric nitrogen−35 , 1984 .

[3]  G. Germain,et al.  Photochemical and Thermal Rearrangement of Oxaziridines - Experimental-evidence in Support of the Stereoelectronic Control-theory , 1982 .

[4]  N. Zaichenko,et al.  Asymmetrical nonbridgehead nitrogen—XXIII: Chiral 3,3-bis(trifluoromethyl)diaziridines , 1982 .

[5]  A. Forni,et al.  Absolute configuration at the chiral nitrogen atom in optically active oxaziridines. X-Ray structure, physical properties, and thermal epimerization of (–)-(2S)– and (+)-(2R)-2-[(R)-α-methylbenzyl]-3,3-diphenyloxaziridines , 1978 .

[6]  A. Forni,et al.  Absolute stereochemistry of the peroxy-acid–imine route to optically active oxaziridines , 1977 .

[7]  E. Borowski,et al.  Studies on the configuration at chiral nitrogen in 2-(S-1-phenylethyl)-3-p-bromophenyl oxaziridine , 1976 .

[8]  D. Mostowicz,et al.  Asymmetric synthesis of oxaziridines , 1975 .

[9]  Harold A. Scheraga,et al.  Intermolecular potentials from crystal data. III. Determination of empirical potentials and application to the packing configurations and lattice energies in crystals of hydrocarbons, carboxylic acids, amines, and amides , 1974 .

[10]  H. Dorn,et al.  Potentielle Cytostatica, XVIII Synthese N′‐substituierter N‐[ω‐Sulfo‐alkyl]‐hydrazine und 2.5‐disubstituierter 1.4‐Bis‐[ω‐sulfo‐alkyl]‐hexahydro‐1.2.4.5‐tetrazine , 1968 .

[11]  C. Paget,et al.  SYNTHESIS AND IN VITRO ACTIVITY OF SOME ARYL DIAZIRIDINES AS POTENTIAL MONOAMINE OXIDASE INHIBITORS. , 1964, Journal of medicinal chemistry.