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For a recent, leading reference concerning olefin aminohydroxylation, see: G. Li, H. H. Angert, K. B. Sharpless, Angew. Chem. 1996, 108, 2995; Angew. Chem. Int. Ed. Engl. 1996, 35, 2813.
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For a recent, leading reference concerning olefin aminohydroxylation, see: G. Li, H. H. Angert, K. B. Sharpless, Angew. Chem. 1996, 108, 2995; Angew. Chem. Int. Ed. Engl. 1996, 35, 2813.
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For comprehensive reviews on transition metal nitrides, see: a) K. Dehnicke, J. Strähle, Angew. Chem. 1992, 104, 978; Angew. Chem. Int. Ed. Engl. 1992, 31, 955; b) W. A. Nugent, J. M. Mayer, Metal-Ligand Multiple Bonds, Wiley Interscience, New York, 1988.
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For comprehensive reviews on transition metal nitrides, see: a) K. Dehnicke, J. Strähle, Angew. Chem. 1992, 104, 978; Angew. Chem. Int. Ed. Engl. 1992, 31, 955; b) W. A. Nugent, J. M. Mayer, Metal-Ligand Multiple Bonds, Wiley Interscience, New York, 1988.
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85088810001
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2(X)] derivatives have been documented, although reliable structural information is often lacking, see ref. [9a]
-
2(X)] derivatives have been documented, although reliable structural information is often lacking, see ref. [9a].
-
-
-
-
26
-
-
0642336760
-
-
note
-
H-3-R-sal-R′ is used to designate substitution on the salicylimine, as shown in Scheme 1.
-
-
-
-
27
-
-
85088810070
-
-
note
-
2Br] gave variable results.
-
-
-
-
28
-
-
0642275509
-
-
note
-
2 = 0.081 with a GOF = 2.135. Hydrogen positions were determined from the difference Fourier map [21 b].
-
-
-
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29
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0001314890
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III complex, see: K. Inamoto, M. Koikawa, M. Nakashima, T. Tokii, Inorg. Chim. Acta 1996, 249, 251.
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37
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0007176888
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2 from low-valent metal azides to generate nitrido metal species have been documented, see: a) T. Jüstel, T. Weyhermüller, K. Wieghardt, E. Bill, M. Lengen, A. X. Trautwein, P. Hildebrandt, Angew. Chem. 1995, 107, 744; Angew. Chem. Int. Ed. Engl. 1995, 34, 669; b) J. W. Buchler, C. Dreher, Z. Naturforsch. B 1984, 39, 222; c) S. I. Arshankow, A. L. Poznjak, Z. Anorg. Allg. Chem. 1981, 481, 201.
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38
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33748222041
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2 from low-valent metal azides to generate nitrido metal species have been documented, see: a) T. Jüstel, T. Weyhermüller, K. Wieghardt, E. Bill, M. Lengen, A. X. Trautwein, P. Hildebrandt, Angew. Chem. 1995, 107, 744; Angew. Chem. Int. Ed. Engl. 1995, 34, 669; b) J. W. Buchler, C. Dreher, Z. Naturforsch. B 1984, 39, 222; c) S. I. Arshankow, A. L. Poznjak, Z. Anorg. Allg. Chem. 1981, 481, 201.
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39
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0345174784
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2 from low-valent metal azides to generate nitrido metal species have been documented, see: a) T. Jüstel, T. Weyhermüller, K. Wieghardt, E. Bill, M. Lengen, A. X. Trautwein, P. Hildebrandt, Angew. Chem. 1995, 107, 744; Angew. Chem. Int. Ed. Engl. 1995, 34, 669; b) J. W. Buchler, C. Dreher, Z. Naturforsch. B 1984, 39, 222; c) S. I. Arshankow, A. L. Poznjak, Z. Anorg. Allg. Chem. 1981, 481, 201.
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Buchler, J.W.1
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40
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84983947204
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2 from low-valent metal azides to generate nitrido metal species have been documented, see: a) T. Jüstel, T. Weyhermüller, K. Wieghardt, E. Bill, M. Lengen, A. X. Trautwein, P. Hildebrandt, Angew. Chem. 1995, 107, 744; Angew. Chem. Int. Ed. Engl. 1995, 34, 669; b) J. W. Buchler, C. Dreher, Z. Naturforsch. B 1984, 39, 222; c) S. I. Arshankow, A. L. Poznjak, Z. Anorg. Allg. Chem. 1981, 481, 201.
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42
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0000472932
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-
Other methods for synthesizing Mn≡N bonds with porphyrin and phthalocyanine complexes have been described, see: a) Hill, C. L.; Hollander, F. J. J. Am. Chem. Soc. 1982, 104, 7318; b) H. Grunewald, H. Homborg, Z. Anorg. Allg. Chem. 1992, 608, 81, and references therein.
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Hill, C.L.1
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43
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84983984181
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and references therein
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Other methods for synthesizing Mn≡N bonds with porphyrin and phthalocyanine complexes have been described, see: a) Hill, C. L.; Hollander, F. J. J. Am. Chem. Soc. 1982, 104, 7318; b) H. Grunewald, H. Homborg, Z. Anorg. Allg. Chem. 1992, 608, 81, and references therein.
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44
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0642306038
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note
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2(N)], respectively). Copies of the data can be obtained free of charge on application to The Director, CCDC, 12 Union Road, Cambridge CB2 1EZ, UK (fax: int. code +(1223) 336-033; e-mail: deposit@chemcrys.cam.ac.uk).
-
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45
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33845550840
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J. W. Buchler, C. Dreher, K.-L. Lay, Y. J. A. Lee, W. R. Scheidt, Inorg. Chem. 1983, 12, 888.
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Buchler, J.W.1
Dreher, C.2
Lay, K.-L.3
Lee, Y.J.A.4
Scheidt, W.R.5
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46
-
-
85088810035
-
-
note
-
V porphyrin and salen complexes.
-
-
-
|