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1
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For reviews on aziridine chemistry see: (a) McCoull, W.; Davis, F. A. Synthesis 2000, 1347.
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(a) Hedley, S. J.; Moran, W. J.; Prenzel, A. H. G. P.; Price, D. A.; Harrity, J. P. A. Synlett 2001, 1596.
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Price, D.A.4
Harrity, J.P.A.5
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(b) Hedley, S. J.; Moran, W. J.; Price, D. A.; Harrity, J. P. A. J. Org. Chem. 2003, 68, 4286.
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(c) Moran, W. J.; Goodenough, K. M.; Raubo, P.; Harrity, J. P. A. Org. Lett. 2003, 5, 3427.
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(d) Goodenough, K. M.; Moran, W. J.; Raubo, P.; Harrity, J. P. A. J. Org. Chem. 2005, 70, 207.
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(e) Goodenough, K. M.; Raubo, P.; Harrity, J. P. A. Org. Lett 2005, 7, 2993.
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S
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(f) Pattenden, L. C.; Wybrow, R. A. J.; Smith, S. A.; Harrity, J. P. A. Org. Lett. 2006, S, 3089.
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(g) Provoost, O. Y.; Hedley, S. J.; Hazelwood, A. J.; Harrity, J. P. A. Tetrahedron Lett. 2006, 47, 331.
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(a) Baldwin, J. E.; Spivey, A. C.; Schofield, C. J.; Sweeney, J. B. Tetrahedron 1993, 49, 6309.
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Sweeney, J.B.4
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24
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0001487357
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The Büchi Grignard reagent 8 has been proposed to exist as a dialkylmagnesium species that can undergo transformations more typical of an organocuprate. For example, 8 can undergo conjugate addition to enones in the absence of Cu-catalysts: Sworin, M; Neumann, W. L
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The Büchi Grignard reagent 8 has been proposed to exist as a dialkylmagnesium species that can undergo transformations more typical of an organocuprate. For example, 8 can undergo conjugate addition to enones in the absence of Cu-catalysts: Sworin, M; Neumann, W. L. Tetrahedron Lett. 1987, 28, 3217.
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(1987)
Tetrahedron Lett
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25
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38849146734
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10b
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10b
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26
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0038370762
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Righi, P.; Scardovi, N.; Marotta, E.; ten Holte, P.; Zwanenburg, B. Org. Lett. 2002, 4, 497.
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Righi, P.1
Scardovi, N.2
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ten Holte, P.4
Zwanenburg, B.5
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27
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0032509407
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3). Alonso, A. A.; Andersson, P. G. J. Org. Chem. 1998, 63, 9455.
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3). Alonso, A. A.; Andersson, P. G. J. Org. Chem. 1998, 63, 9455.
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28
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38849207216
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The stereochemistry of compounds 25, 26, and 27 has been elucidated by X-ray crystallography. CCDC 659299, CCDC 659300, and CCDC 661089 contain the supplementary crystallographic data for 25, 26, and 27, respectively. This data can be obtained free of charge via www.ccdc.cam.ac.uk/conts/retrieving.html (or from the Cambridge Crystallographic Data Centre, 12 Union Road, Cambridge, CB2 1EZ, UK; fax (+44) 1223-336-033; or request@ccdc.cam.ac.uk).
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The stereochemistry of compounds 25, 26, and 27 has been elucidated by X-ray crystallography. CCDC 659299, CCDC 659300, and CCDC 661089 contain the supplementary crystallographic data for 25, 26, and 27, respectively. This data can be obtained free of charge via www.ccdc.cam.ac.uk/conts/retrieving.html (or from the Cambridge Crystallographic Data Centre, 12 Union Road, Cambridge, CB2 1EZ, UK; fax (+44) 1223-336-033; or request@ccdc.cam.ac.uk).
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