Organic Letters
Letter
have been demonstrated, and a stereochemical model has been
proposed based on preliminary computational analysis.
Application of this tactic using complex sulfur ylide reagents
for entry to aziridine carboxylates containing vicinal stereo-
centers is underway and will be reported in due course.
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2
(
(
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ASSOCIATED CONTENT
Supporting Information
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S
(11) (a) Muller, P.; Fruit, C. Chem. Rev. 2003, 103, 2905. (b) Duan, P.-
W.; Chiu, C.-C.; Lee, W.-D.; Pan, L. S.; Venkatesham, U.; Tzeng, Z.-H.;
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X-ray structure of 4h (CIF)
X-ray structure of 5i (CIF)
X-ray structure of 14 (CIF)
1
996, 35, 1848. (g) Kano, T.; Sakamoto, R.; Mii, H.; Wang, Y.-G.;
AUTHOR INFORMATION
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Maruoka, K. Tetrahedron 2010, 66, 4900. (h) Miniejew, C.; Outurquin,
F.; Pannecoucke, X. Tetrahedron 2006, 62, 2657. (i) Sharma, S. D.;
Kanwar, S.; Rajpoot, S. J. Heterocycl. Chem. 2006, 43, 11.
Notes
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12) (a) Patwardhan, A. P.; Pulgam, V. R.; Zhang, Y.; Wulff, W. D.
Angew. Chem., Int. Ed. 2005, 44, 6169. (b) Alezra, V.; Bonin, M.;
Micouin, L.; Husson, H.-P. Tetrahedron Lett. 2000, 41, 651.
The authors declare no competing financial interest.
(
13) Deiana, L.; Zhao, G.-L.; Lin, S.; Dziedzic, P.; Zhang, Q.;
Leijonmarck, H.; Cordova, A. Adv. Synth. Catal. 2010, 352, 3201.
14) McNally, A.; Haffemayer, B.; Collins, B. S. L.; Gaunt, M. J. Nature
014, 510, 129.
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