Transition metal catalyzed manipulation of non-polar carbon–hydrogen bonds for synthetic purpose
Author:
Affiliation:
1. Nara Institute of Science and Technology (NAIST)
Publisher
Japan Academy
Subject
General Physics and Astronomy,General Agricultural and Biological Sciences,General Medicine
Link
https://www.jstage.jst.go.jp/article/pjab/87/5/87_5_230/_pdf
Reference96 articles.
1. 1) Kleiman, J.P. and Dubeck, M. (1963) The preparation of cyclopentadienyl [o-(phenylazo)phenyl]nickel. J. Am. Chem. Soc. 85, 1544–1545.
2. 2) Chatt, J. and Watson, H.R. (1962) Complexes of zerovalent transtition metals with the ditertiary phosphine, Me2·PCH2·CH2·PMe2. J. Chem. Soc., 2545–2549.
3. 3) Chatt, J. and Davidson, J.M. (1965) The tautomerism of arene and ditertiary phosphine complexes of ruthenium(0), and the preparation of new types of hydrido-complex of ruthenium(II). J. Chem. Soc., 843–855.
4. 4) La Placa, S.J. and Ibers, J.A. (1965) Five-coordinate d6 complex: structure of dichlorotris(triphenylphosphine)ruthenium(II). Inorg. Chem. 4, 778–783.
5. 5) Bergman, R.G. (1984) Activation of alkanes with organotransition metal complexes. Science 223, 902–908.
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