氧氮環丙烷 (Chinese Wikipedia)

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Davis, F. A.; Sheppard, A. C. Applications of oxaziridines in organic synthesis. Tetrahedron. 1989, 45 (18): 5703. doi:10.1016/s0040-4020(01)89102-x.
Davis, F. A.; Weismiller, M. C.; Lal, G. S.; Chen, B. C.; Przeslawski, R. M. (Camphorylsulfonyl)imine dianion in the synthesis of new optically pure (camphorylsulfonyl)oxaziridine derivatives. Tetrahedron Letters. 1989, 30 (13): 1613. doi:10.1016/s0040-4039(00)99534-0.
Aubé, Jeffrey. Oxiziridine rearrangements in asymmetric synthesis. Chemical Society Reviews. 1997, 26 (4): 269. doi:10.1039/CS9972600269.

doi.org

Emmons, W. D. J. Am. Chem. Soc. 1956, 78 (23): 6208. doi:10.1021/ja01604a072. 缺少或|title=为空 (帮助)
Horner, L.; Jürgens, E. Notiz Über Darstellung und Eigenschaften Einiger Isonitrone (Oxazirane). Chemische Berichte. 1957, 90 (10): 2184. doi:10.1002/cber.19570901010.
Davis, F. A.; Sheppard, A. C. Applications of oxaziridines in organic synthesis. Tetrahedron. 1989, 45 (18): 5703. doi:10.1016/s0040-4020(01)89102-x.
Davis, F. A.; Stringer, O. D. Chemistry of oxaziridines. 2. Improved synthesis of 2-sulfonyloxaziridines. The Journal of Organic Chemistry. 1982, 47 (9): 1774. doi:10.1021/jo00348a039.
Davis, F. A.; Chattopadhyay, S.; Towson, J. C.; Lal, S.; Reddy, T. Chemistry of oxaziridines. 9. Synthesis of 2-sulfonyl- and 2-sulfamyloxaziridines using potassium peroxymonosulfate (oxone). The Journal of Organic Chemistry. 1988, 53 (9): 2087. doi:10.1021/jo00244a043.
Davis, F. A.; Chen, B. C. Asymmetric hydroxylation of enolates with N-sulfonyloxaziridines. Chem. Rev. 1992, 92 (5): 919. doi:10.1021/cr00013a008.
Davis, F. A.; Jenkins, R. H.; Awad, S. B.; Stringer, O. D.; Watson, W. H.; Galloy, J. Chemistry of oxaziridines. 3. Asymmetric oxidation of organosulfur compounds using chiral 2-sulfonyloxaziridines. Journal of the American Chemical Society. 1982, 104 (20): 5412. doi:10.1021/ja00384a028.
Davis, F. A.; Reddy, R. T.; McCauley, J. P.; Przeslawski, R. M.; Harakal, M. E.; Carroll, P. J. Chemistry of oxaziridines. 15. Asymmetric oxidations using 3-substituted 1,2-benzisothiazole 1,1-dioxide oxides. The Journal of Organic Chemistry. 1991, 56 (2): 809. doi:10.1021/jo00002a056.
Davis, F. A.; Towson, J. C.; Weismiller, M. C.; Lal, S.; Carroll, P. J. Chemistry of oxaziridines. 11. (Camphorylsulfonyl)oxaziridine: synthesis and properties. Journal of the American Chemical Society. 1988, 110 (25): 8477. doi:10.1021/ja00233a025.
Bach, R. D.; Coddens, B. A.; McDouall, J. J. W.; Schlegel, H. B.; Davis, F. A. The mechanism of oxygen transfer from an oxaziridine to a sulfide and a sulfoxide: a theoretical study. The Journal of Organic Chemistry. 1990, 55 (10): 3325. doi:10.1021/jo00297a062.
Davis, F. A.; Kumar, A.; Chen, B. C. Chemistry of oxaziridines. 16. A short, highly enantioselective synthesis of the AB-ring segments of .gamma.-rhodomycionone and .alpha.-citromycinone using (+)-[(8,8-dimethoxycamphoryl)sulfonyl]oxaziridine. The Journal of Organic Chemistry. 1991, 56 (3): 1143. doi:10.1021/jo00003a042.
Davis, F. A.; Weismiller, M. C.; Lal, G. S.; Chen, B. C.; Przeslawski, R. M. (Camphorylsulfonyl)imine dianion in the synthesis of new optically pure (camphorylsulfonyl)oxaziridine derivatives. Tetrahedron Letters. 1989, 30 (13): 1613. doi:10.1016/s0040-4039(00)99534-0.
Chen, B. C.; Weismiller, M. C.; Davis, F. A.; Boschelli, D.; Empfield, J. R.; Smith, A. B. Enantioselective synthesis of (+)-kjellmanianone. Tetrahedron. 1991, 47 (2): 173–82. doi:10.1016/S0040-4020(01)80914-5.
Petrov, V. A.; Resnati, G. Polyfluorinated Oxaziridines: Synthesis and Reactivity. Chemical Reviews. 1996, 96 (5): 1809. doi:10.1021/cr941146h.
Evans, D. A.; Morrissey, M. M.; Dorow, R. L. Asymmetric oxygenation of chiral imide enolates. A general approach to the synthesis of enantiomerically pure .alpha.-hydroxy carboxylic acid synthons. journal of the American Chemical Society. 1985, 107 (14): 4346. doi:10.1021/ja00300a054.
Dounay, Amy B.; Forsyth, Craig J. Abbreviated Synthesis of the C3−C14 (Substituted 1,7-Dioxaspiro[5.5]undec-3-ene) System of Okadaic Acid. Org. Lett. 1999, 1 (3): 451. doi:10.1021/ol9906615.
Malgesini, Beatrice; Forte, Barbara; Borghi, Daniela; Quartieri, Francesca; Gennari, Cesare; Papeo, Gianluca. A Straightforward Total Synthesis of (−)-Chaetominine. Chem. Eur. J. 2009, 15 (32): 7922. doi:10.1002/chem.200900793.
Bohé, Luis; Hanquet, Gilles; Lusinchi, Marie; Lusinchi, Xavier. The stereospecific synthesis of a new chiral oxaziridinium salt. Tetrahedron Letters. 1993, 34 (45): 7271. doi:10.1016/S0040-4039(00)79306-3.
Arnone, Alberto; Foletto, Stefania; Metrangolo, Pierangelo; Pregnolato, Massimo; Resnati, Giuseppe. Highly Enantiospecific Oxyfunctionalization of Nonactivated Hydrocarbon Sites by Perfluoro-cis-2-n-butyl-3-n-propyloxaziridine. Org. Lett. 1999, 1 (2): 281. doi:10.1021/ol990594e.
Schmitz, E.; Ohme, R. Isomere Oxime mit Dreiringstruktur. Chem. Ber. 1964, 97 (9): 2521. doi:10.1002/cber.19640970916.
Andreae, S.; Schmitz, E. ChemInform Abstract: Electrophilic Aminations with Oxaziridines. ChemInform. 1991, 22 (46): 327. doi:10.1002/chin.199146339.
Aubé, Jeffrey. Oxiziridine rearrangements in asymmetric synthesis. Chemical Society Reviews. 1997, 26 (4): 269. doi:10.1039/CS9972600269.
Lattes, Armand; Oliveros, Esther; Riviere, Monique; Belzeck, Czeslaw; Mostowicz, Danuta; Abramskj, Wojciech;Piccinni-Leopardi, Carla; Germain, Gabriel; Van Meerssche, Maurice. Photochemical and thermal rearrangement of oxaziridines. Experimental evidence in support of the stereoelectronic control theory. Journal of the American Chemical Society. 1982, 104 (14): 3929. doi:10.1021/ja00378a024.

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pubchem.ncbi.nlm.nih.gov

CID 15817734 - PubChem Public Chemical Database. The PubChem Project. USA: National Center for Biotechnology Information. [2013-07-11]. （原始内容存档于2012-11-03）.

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CID 15817734 - PubChem Public Chemical Database. The PubChem Project. USA: National Center for Biotechnology Information. [2013-07-11]. （原始内容存档于2012-11-03）.