Self-Assembled Poly(imidazole-palladium): Highly Active, Reusable Catalyst at Parts per Million to Parts per Billion Levels

Yoichi M. A. Yamada; Shaheen M. Sarkar; Yasuhiro Uozumi

doi:10.1021/ja210772v

journal article Feb 03, 2012

Self-Assembled Poly(imidazole-palladium): Highly Active, Reusable Catalyst at Parts per Million to Parts per Billion Levels

Yoichi M. A. Yamada

Shaheen M. Sarkar Yasuhiro Uozumi

Journal of the American Chemical Society Vol. 134 No. 6 pp. 3190-3198 · American Chemical Society (ACS)

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References

78

[1]

Sadava D. (2009)

[2]

Reetz M. T. Proc. Natl. Acad. Sci. U. S. A. (2004) 10.1073/pnas.0306866101

[3]

Mikami K. (2007) 10.1002/0470098007

[4]

Crabtree R. H. (2009)

[5]

Uozumi Y. (2002)

[6]

Franzel T. (2003)

[7]

Uozumi Y. Top. Curr. Chem. (2004) 10.1007/b96874

[8]

Wennemers H. (2004) 10.1002/3527603727.ch5d

[9]

Wang Z. Chem. Rev. (2009) 10.1021/cr800406u

[10]

Lu J. Chem. Rev. (2009) 10.1021/cr8004444

[11]

Baer K. Angew. Chem., Int. Ed. (2009) 10.1002/anie.200900582

[12]

Uozumi Y. Chem. Rec. (2009) 10.1002/tcr.20165

[13]

Lamblin M. Adv. Synth. Catal. (2010) 10.1002/adsc.200900765

[14]

Yamada Y. M. A. J. Synth. Org. Chem., Jpn (2011) 10.5059/yukigoseikyokaishi.69.542

[15]

Williams R. J. P. Pure Appl. Chem. (1974) 10.1351/pac197438010249

[16]

Benson D. E. Curr Opin. Biotechnol. (1998) 10.1016/s0958-1669(98)80010-4

[17]

Tadokoro M. Coord. Chem. Rev. (2000) 10.1016/s0010-8545(99)00223-4

[18]

Navarroa J. A. R. Coord. Chem. Rev. (2001) 10.1016/s0010-8545(01)00390-3

[19]

Bolon D. N. Curr. Opin. Chem. Biol. (2002) 10.1016/s1367-5931(02)00303-4

[20]

Kitagawa S. Angew. Chem., Int. Ed. (2004) 10.1002/anie.200300610

[21]

Branta J. A. J. Mol. Struct. (2006) 10.1016/j.molstruc.2006.02.064

[22]

Lin W. Angew. Chem., Int. Ed. (2009) 10.1002/anie.200803387

[23]

Ueno T. Angew. Chem., Int. Ed. (2010) 10.1002/anie.201000337

[24]

Niele F. G. M. J. Am. Chem. Soc. (1988) 10.1021/ja00209a027

[25]

Dobrzanska L. J. Am. Chem. Soc. (2005) 10.1021/ja054119p

[26]

Lo Y.-S. Thin Solid Films (2008) 10.1016/j.tsf.2007.06.156

[27]

Imaz I. Angew. Chem., Int. Ed. (2009) 10.1002/anie.200804255

[28]

Yang L. Chem. Commun. (2010) 10.1039/c0cc00112k

[29]

Zambelli B. Acc. Chem. Res. (2011) 10.1021/ar200041k

[30]

Yamada Y. M. A. Chem. Pharm. Bull. (2005) 10.1248/cpb.53.723

[31]

Yamada Y. M. A. Org. Lett. (2006) 10.1021/ol060166q

[32]

Uozumi Y. J. Am. Chem. Soc. (2006) 10.1021/ja066697r

[33]

Yamada Y. M. A. Org. Lett. (2006) 10.1021/ol0615026

[34]

Yamada Y. M. A. Org. Lett. (2007) 10.1021/ol070258v

[35]

Yamada Y. M. A. Tetrahedron (2007) 10.1016/j.tet.2007.05.071

[36]

Yamada Y. M. A. Org. Lett. (2010) 10.1021/ol101839m

[37]

Ohta H. Org. Lett. (2011) 10.1021/ol201422s

[38]

Sarkar S. M. Angew. Chem., Int. Ed. (2011) 10.1002/anie.201103799

[39]

Mattiasson B. Nature Prot. (2007) 10.1038/nprot.2006.440

[40]

Tsukamoto H. Chem. Commun. (2004) 10.1039/b402256d

[41]

Néjera C. Adv. Synth. Catal. (2004) 10.1002/adsc.200404195

[42]

Manabe K. Adv. Synth. Catal. (2005) 10.1002/adsc.200505135

[43]

Monreno-Mañas M. Organometallics (2001) 10.1021/om010442z

[44]

Kabalka G. W. Org. Lett. (2003) 10.1021/ol034067d

[45]

Paetzold E. J. Mol. Catal. A (2000) 10.1016/s1381-1169(99)00286-1

[46]

Blart E. Tetrahedon Lett (1994) 10.1016/s0040-4020(01)80772-9

[47]

Miyaura N. J. Am. Chem. Soc. (1985) 10.1021/ja00290a037

[48]

Ohmiya H. J. Am. Chem. Soc. (2010) 10.1021/ja9092264

[49]

Ohmiya H. J. Am. Chem. Soc. (2008) 10.1021/ja808673n

[50]

Orar G. Tetrahedron Lett. (2003) 10.1016/s0040-4039(03)00980-8

Showing 50 of 78 references

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Details

Published: Feb 03, 2012
Vol/Issue: 134(6)
Pages: 3190-3198

Authors

Y

Yoichi M. A. Yamada

RIKEN Advanced Science Institute, Wako, Saitama 351-0198, Japan

S

Shaheen M. Sarkar

RIKEN Advanced Science Institute, Wako, Saitama 351-0198, Japan

Y

Yasuhiro Uozumi

RIKEN Advanced Science Institute, Wako, Saitama 351-0198, Japan; Institute for Molecular Science and the Graduate School for Advanced Studies, Okazaki, Aichi 444-8787, Japan

Cite This Article

Yoichi M. A. Yamada, Shaheen M. Sarkar, Yasuhiro Uozumi (2012). Self-Assembled Poly(imidazole-palladium): Highly Active, Reusable Catalyst at Parts per Million to Parts per Billion Levels. Journal of the American Chemical Society, 134(6), 3190-3198. https://doi.org/10.1021/ja210772v

Self-Assembled Poly(imidazole-palladium): Highly Active, Reusable Catalyst at Parts per Million to Parts per Billion Levels

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