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(en) P. A. Wender, N. F. Badhamet al., « The pinene path to taxanes. 5. Stereocontrolled synthesis of a versatile taxane precursor », J. Am. Chem. Soc., vol. 119, no 11, , p. 2755–2756 (ISSN0002-7863 et 1520-5126, DOI10.1021/ja9635387).
(en) A. B. Dounay et C. J. Forsyth, « Abbreviated synthesis of the C3−C14 (substituted 1,7-dioxaspiro[5.5]undec-3-ene) system of okadaic acid », Org. Lett., vol. 1, no 3, , p. 451–454 (ISSN1523-7060 et 1523-7052, DOI10.1021/ol9906615).
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(en) P. A. Wender, N. F. Badhamet al., « The pinene path to taxanes. 5. Stereocontrolled synthesis of a versatile taxane Precursor », J. Am. Chem. Soc., vol. 119, no 11, , p. 2755–2756 (ISSN0002-7863 et 1520-5126, DOI10.1021/ja9635387).
(en) F. A. Davis, S. Chattopadhyayet al., « Chemistry of oxaziridines. 9. Synthesis of 2-sulfonyl- and 2-sulfamyloxaziridines using potassium peroxymonosulfate (oxone) », J. Org. Chem., vol. 53, no 9, , p. 2087–2089 (ISSN0022-3263 et 1520-6904, DOI10.1021/jo00244a043).
(en) F. A. Davis et R. H. Jenkins, « Chemistry of oxaziridines. 3. Asymmetric oxidation of organosulfur compounds using chiral 2-sulfonyloxaziridines », J. Am. Chem. Soc., vol. 104, no 20, , p. 5412–5418 (ISSN0002-7863 et 1520-5126, DOI10.1021/ja00384a028).
(en) F. A. Davis, R. T. Reddyet al., « Chemistry of oxaziridines. 15. Asymmetric oxidations using 3-substituted 1,2-benzisothiazole 1,1-dioxide oxides », J. Org. Chem., vol. 56, no 2, , p. 809–815 (ISSN0022-3263 et 1520-6904, DOI10.1021/jo00002a056).
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(en) F. A. Davis, A. Kumaret al., « Chemistry of oxaziridines. 16. A short, highly enantioselective synthesis of the AB-ring segments of γ-rhodomycionone and α-citromycinone using (+)-[(8,8-dimethoxycamphoryl)sulfonyl]oxaziridine », J. Org. Chem., vol. 53, no 3, , p. 1143–1145 (ISSN0022-3263 et 1520-6904, DOI10.1021/jo00003a042).
(en) F. A. Davis, M. C. Weismilleret al., « (Camphorylsulfonyl)imine dianion in the synthesis of new optically pure (camphorylsulfonyl)oxaziridine derivatives », Tetrahedron Lett., vol. 30, no 13, , p. 1613–1616 (ISSN0040-4039, DOI10.1016/S0040-4039(00)99534-0).
(en) D. A. Evans, M. M. Morrisseyet al., « Asymmetric oxygenation of chiral imide enolates. A general approach to the synthesis of enantiomerically pure α-hydroxy carboxylic acid synthons », J. Am. Chem. Soc., vol. 107, no 14, , p. 4346–4348 (ISSN0002-7863 et 1520-5126, DOI10.1021/ja00300a054).
(en) P. A. Wender, N. F. Badhamet al., « The pinene path to taxanes. 5. Stereocontrolled synthesis of a versatile taxane precursor », J. Am. Chem. Soc., vol. 119, no 11, , p. 2755–2756 (ISSN0002-7863 et 1520-5126, DOI10.1021/ja9635387).
(en) A. B. Dounay et C. J. Forsyth, « Abbreviated synthesis of the C3−C14 (substituted 1,7-dioxaspiro[5.5]undec-3-ene) system of okadaic acid », Org. Lett., vol. 1, no 3, , p. 451–454 (ISSN1523-7060 et 1523-7052, DOI10.1021/ol9906615).
(en) A. Arnone, S. Folettoet al., « Highly enantiospecific oxyfunctionalization of nonactivated hydrocarbon sites by perfluoro-cis-2-n-butyl-3-n-propyloxaziridine », Org. Lett., vol. 1, no 2, , p. 281–284 (ISSN1523-7060 et 1523-7052, DOI10.1021/ol990594e).
(en) A. Lattes, E. Oliveroset al., « Photochemical and thermal rearrangement of oxaziridines. Experimental evidence in support of the stereoelectronic control theory », J. Am. Chem. Soc., vol. 104, no 14, , p. 3929–3934 (ISSN0002-7863 et 1520-5126, DOI10.1021/ja00378a024).
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