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Most Type I palladacycles are known to exist as bridged dimers and to dissociate into monomeric forms during reactions. All Type I pallada-cycles in this paper were drawn in monomeric forms
-
Most Type I palladacycles are known to exist as bridged dimers and to dissociate into monomeric forms during reactions. All Type I pallada-cycles in this paper were drawn in monomeric forms.
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5
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3 catalyst: (a) Cho, C. S.; Motofusa, S.; Ohe, K.; Uemura, S. J. Org. Chem. 1995, 60, 883-888.
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For cationic Pd(II) catalysts: (b) Nishikata, T.; Yamamoto, Y.; Gridnev, I. D.; Miyaura, N. Organometallics 2005, 24, 5025-5032.
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2/pyridine catalyst: (e) Lu, X.; Lin, S. J. Org. Chem. 2005, 70, 9651-9653.
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3)2/(R,R)-Me-Duphos catalyst: (f) Gini, F.; Hessen, B.; Minnaard, A. J. Org. Lett. 2005, 7, 5309-5312.
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3 catalyst: (g) Yamamoto, T.; Iizuka, M.; Ohta, T.; Ito, Y. Chem. Lett. 2006, 35, 198-199.
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3-catalyzed 1,2-addition of arylboronic acids with aldehydes at elevated temperature: Yamamoto, T.; Ohio, T.; Ito, Y. Org. Lett. 2005, 7, 4153-4155.
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One example of 1,2-addition products of phenylboronic acid with p-chlorobenzaldehyde, formed as byproducts during the cross-coupling reaction catalyzed by a palladacycle at 130°C, was previously reported: Gibson, S.; Foster, D. F.; Eastham, G. R.; Tooze, R. P.; Cole-Hamilton, D. J. Chem. Commun. 2001, 779-780.
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One example of 1,2-addition products of phenylboronic acid with p-chlorobenzaldehyde, formed as byproducts during the cross-coupling reaction catalyzed by a palladacycle at 130°C, was previously reported: Gibson, S.; Foster, D. F.; Eastham, G. R.; Tooze, R. P.; Cole-Hamilton, D. J. Chem. Commun. 2001, 779-780.
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Selected recent examples of Rh(I)-catalyzed 1,4-additions of aryl-boronic acids with α,β-unsaturated compounds - with chiral dienes as ligands: (a) Trenkle, W. C.; Barkin, J. L.; Son, S. U.; Sweigart, D. A. Organometallics 2006, 25, 3548-3551.
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2; for its characterization, see the Supporting Information.
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2; for its characterization, see the Supporting Information.
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For examples of protonation of palladium(II) enolates see refs 4b and 16. Also see: (a) Hamashima, Y.; Hotta, D.; Sodeoka, M. J. Am. Chem. Soc. 2002, 124, 11240-11241.
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For anionic six-electron donor-based (Type II) palladacycle-catalyzed allylic additions of aldehydes and imines: (a) Solin, N.; Wallner, O. A.; Szabo, K. J. Org. Lett. 2005, 7, 689-691.
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