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Trofimenko, S.1
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Otero A., Fernàndez-Baeza J., Antiñolo A., Tejeda J., Lara-Sànchez A., Sànchez-Barba L., Sànchez-Molina M., Franco S., Lopez-Solera I., and Rodríguez A.M. Dalton Trans. (2006) 4359
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For synthesis and application of trisoxazolines and their metal complexes see:
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For synthesis and application of trisoxazolines and their metal complexes see:. Gade L.H., and Bellemin-Laponnaz S. Chem. Eur. J. 14 (2008) 4142
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Foltz C., Stecker B., Marconi G., Bellemin-Laponnaz S., Wadepohl H., and Gade L.H. Chem. Commun. (2005) 5115
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Foltz, C.1
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For related pincer complexes see:. Bugarin A., and Connell B.T. Organometallics 27 (2008) 4357
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47149089299
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It has also been shown that bisoxazolines can undergo aerobic oxidation in the presence of zinc to form sidearm substituted metallamacrocycles:
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It has also been shown that bisoxazolines can undergo aerobic oxidation in the presence of zinc to form sidearm substituted metallamacrocycles:. Jacques B., Dro C., Bellemin-Laponnaz S., Wadepohl H., and Gade L.H. Angew. Chem., Int. Ed. 47 (2008) 4546
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For preparation of 2-(tert-butyldimethylsilyoxy)benzyl bromide see experimental. Adapted from:
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For preparation of 2-(tert-butyldimethylsilyoxy)benzyl bromide see experimental. Adapted from:. Heslin J.C., and Moody C.J. J. Chem. Soc. Perkin. Trans. I. (1988) 1417
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Chloromethylpyridine is commercially available as the hydrochloride salt which is easily converted to the unstable 2-chloromethylpyridine compound according to:
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Chloromethylpyridine is commercially available as the hydrochloride salt which is easily converted to the unstable 2-chloromethylpyridine compound according to:. Gan X.M., Binyamin I., Rapko B.M., Fox J., Duesler E.N., and Paine R.T. Inorg. Chem. 43 (2004) 2443
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For a recent study of the different coordination isomers of trispyrazolylborate rhodium complexes see:
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