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0001772726
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10 A radical spices reacted at the tricarbonylchromium-complexed arene ring or styrene double bond: Schmalz, H-G.; Siegel, S.; Bats, J. W. Angew. Chem. Int. Ed. Engl. 1995, 34, 2383-2385.
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11 (a) Girad, P.; Namy, J. L.; Kagan, H. B. J. Am. Chem. Soc. 1980, 102, 2693-2698.
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0027386671
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14 A related phenyl-carbonyl coupling product, 4-(α-hydroxybenzyl)benzaldehyde, was obtained as a major product by the treatment of benzaldehyde with samarium diiodide in the presence of HMPA; Shieu, J-S.; Lin, C-C.; Fang, J-M. Tetrahedron Lett. 1993, 34, 335-338; J. Org. Chem. 1997, 02, 4643.
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0010330111
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14 A related phenyl-carbonyl coupling product, 4-(α-hydroxybenzyl)benzaldehyde, was obtained as a major product by the treatment of benzaldehyde with samarium diiodide in the presence of HMPA; Shieu, J-S.; Lin, C-C.; Fang, J-M. Tetrahedron Lett. 1993, 34, 335-338; J. Org. Chem. 1997, 02, 4643.
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43
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85038543143
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note
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15 The authors have deposited ORTEP drawing, atomic coordinates, bond, angles and bond lenghts for the copounds to Director, Cambridge Crystallographic Data Centre, 12 Union Road, Cambridge, CB2 1Ez. UK..
-
-
-
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44
-
-
85038553460
-
-
note
-
16 The first symbol indicates the configuration of planar chirality at the ipso-position of the chromium complexed left-side arene, and the second one represents the configuration at the benzylic position. The symbol (*) indicates racemic compound and only one enantiomer is shown for clarity.
-
-
-
-
45
-
-
37049086391
-
-
17 Optical resolution of the racemic tricarbonylchromium complexes of o-bromobenzaldehyde and o-methylbenzaldehyde was achieved by column chromatographic separation of the corresponding diastereomeric imines derived with (L)-valinol; (a) Davies, S. G.; Goodfellow, C. L. J. Chem. Soc. Perkin Trans 1 1989, 192-194;
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Goodfellow, C.L.2
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0026101096
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(b) Bromley, L. A.; Davies, S. G.; Goodfellow, C. L. Tetrahedron Asymmetry 1991, 2, 139-156.
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85034533375
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18 For a review concerning the mechanism on acyclic selection in the intermolecular radical reactions, namely steric vs electronic controls: Smadja, W. Synlett. 1994, 1-26.
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Synlett.
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Smadja, W.1
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52
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85038550838
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note
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3); δ for 20 (R = Me); 2.10 (6H, s), 2.24 (2H, br), 3.99-4.07 (6H, m), 4.14 (10H, s), 4.21 (2H, s), for 21 (R = Me); 1.69 (3H, s), 1.77 (3H, s), 2.38 (2H, br), 3.99-4.07 (6H, m), 4.10 (5H, s), 4.11 (5H, s), 4.44 (2H, br).
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53
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0000715061
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26 Enantiomerically pure aldimine complexes 29 were prepared from the corresponding resolved enantiomerically pure (o-subsituted benzaldehyde)chromium complexes and primary amines: Kündig, E. P.; Xu, L. H.; Romanens, P.; Bernardinelli, G. Synlett. 1996, 270-272.
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