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44149103947
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For general reviews, see:
-
For general reviews, see:
-
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24
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32644440329
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For a review on σ-Chelation-directed C-H functionalizations, see:
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Dick A.R., and Sanford M.S. Tetrahedron 62 (2006) 2439 For a review on σ-Chelation-directed C-H functionalizations, see:
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36148938653
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During the 15th European Symposium of Organic Chemistry (Dublin, July 2007), we became aware of preliminary direct arylation studies on a protected and unprotected adenosine by the Hocek group in Prague. This group later reported these studies as a communication (available online 25th October 2007), see:
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During the 15th European Symposium of Organic Chemistry (Dublin, July 2007), we became aware of preliminary direct arylation studies on a protected and unprotected adenosine by the Hocek group in Prague. This group later reported these studies as a communication (available online 25th October 2007), see:. Čerňa I., Pohl R., and Hocek M. Chem. Commun. (2007) 4729
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Čerňa, I.1
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44149098705
-
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note
-
1/2 value is expected to fall dramatically in the presence of a base.
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30
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33846064670
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44149094142
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note
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2 in the oxidative dimerisation of purine heterocycles, see Ref. 12.
-
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36
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-
44149104687
-
-
note
-
This palladium(0) complex is available through Sigma-Aldrich (Cat. No. 656933).
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37
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0000840737
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Amatore C., Jutand A., Khalil F., M'Barki M.A., and Mottier L. Organometallics 12 (1993) 3168
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33845228401
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34548191025
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For interesting effects of dibenzylidene acetone ligands, see:
-
Fairlamb I.J.S., and Lee A.F. Organometallics 26 (2007) 4087 For interesting effects of dibenzylidene acetone ligands, see:
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(2007)
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Fairlamb, I.J.S.1
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22144471521
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Professor Marta Catellani commented on this phenomenon at the European Symposium of Organic Chemistry (Dublin, July 2007). For related references, see:
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Professor Marta Catellani commented on this phenomenon at the European Symposium of Organic Chemistry (Dublin, July 2007). For related references, see:. Catellani M., Motti E., Faccini F., and Ferraccioli R. Pure Appl. Chem. 77 (2005) 1243
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48
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44149100596
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Representative examples, see:
-
Representative examples, see:
-
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50
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37049100869
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Jones R.A., Real F.M., Wilkinson G., Galas A.M.R., and Hursthouse M.B. J. Chem. Soc., Dalton Trans. (1981) 126
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For catalytic applications of PVP-stabilised palladium nanoparticles, see:
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Narayanan R., and El-Sayed M.A. J. Am. Chem. Soc. 125 (2003) 8340 For catalytic applications of PVP-stabilised palladium nanoparticles, see:
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44149095352
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A subtle ligand substituent effect on pyridine has also been observed in Pd(II) catalysed aerobic oxidative annulations of indoles. It is believed that certain electron-deficient pyridines make the Pd(II) catalyst more electrophilic and reactive, see:
-
A subtle ligand substituent effect on pyridine has also been observed in Pd(II) catalysed aerobic oxidative annulations of indoles. It is believed that certain electron-deficient pyridines make the Pd(II) catalyst more electrophilic and reactive, see:
-
-
-
-
65
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-
0041624424
-
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It is likely that 3-nitropyridine could play a similar role in the cross-coupling of N-acetylindoles and arenes {as well as stabilising Pd(0)}, see:
-
Ferreira E.M., and Stoltz B.M. J. Am. Chem. Soc. 125 (2003) 9578 It is likely that 3-nitropyridine could play a similar role in the cross-coupling of N-acetylindoles and arenes {as well as stabilising Pd(0)}, see:
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Ferreira, E.M.1
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44149087703
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note
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Private communication from Professor Keith Fagnou (University of Toronto, Canada).
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Pivsa-Art S., Satoh T., Kawamura Y., Miura M., and Nomura M. Bull. Chem. Soc. Jpn. 71 (1998) 467
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4244179585
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Amine coordination is possible. For palladium(II) complexes containing deoxyadenosine the interaction is weak, see:
-
Amine coordination is possible. For palladium(II) complexes containing deoxyadenosine the interaction is weak, see:. Camboli D., Besancon J., Tirouflet J., Gautheron B., and Meunier P. Inorg. Chim. Acta 78 (1983) L51
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33847039568
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For inverse correlations in Sonogashira cross-couplings, see: Ref. 30b; For inverse correlations in carbonylation, see:
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For inverse correlations in Sonogashira cross-couplings, see: Ref. 30b; For inverse correlations in carbonylation, see:. Fairlamb I.J.S., Grant S., McCormack P., and Whittall J. Dalton Trans. (2007) 859
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de Vries A.H.M., Mulders J.M.C.A., Mommers J.H.M., Henderickx H.J.W., and de Vries J.G. Org. Lett. 5 (2003) 3285
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Stanforth S.P. Tetrahedron 54 (1998) 263 and references cited therein
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Stanforth, S.P.1
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Amatore, C.1
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24944485087
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2/C, Pearlman's catalyst) effectively mediates the direct arylation reactions, the active catalyst being a homogeneous one, see:
-
2/C, Pearlman's catalyst) effectively mediates the direct arylation reactions, the active catalyst being a homogeneous one, see:. Parisien M., Valette D., and Fagnou K. J. Org. Chem. 70 (2005) 7578
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34248529661
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a<16), thus the conjugate base predominantly exists as 2-isocyanophenolate, see:
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a<16), thus the conjugate base predominantly exists as 2-isocyanophenolate, see:. Sánchez R.S., and Zhuravlev F.A. J. Am. Chem. Soc. 129 (2007) 5824
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