-
17
-
-
0033533931
-
-
Trifonov A.A., Kirillov E.N., Fischer A., Edelmann F.T., and Bochkarev M.N. Chem. Commun. (1999) 2203
-
(1999)
Chem. Commun.
, pp. 2203
-
-
Trifonov, A.A.1
Kirillov, E.N.2
Fischer, A.3
Edelmann, F.T.4
Bochkarev, M.N.5
-
18
-
-
0031186811
-
-
Brintzinger H.H., Schneider N., Huttenloch M.E., Stehling U., Kirsten R., and Schaper F. Organometallics 16 (1997) 3413
-
(1997)
Organometallics
, vol.16
, pp. 3413
-
-
Brintzinger, H.H.1
Schneider, N.2
Huttenloch, M.E.3
Stehling, U.4
Kirsten, R.5
Schaper, F.6
-
19
-
-
0000748027
-
-
Bercaw J.E., Shapiro P.J., Cotter D., Schaefer W.P., and Labinger J.A. J. Am. Chem. Soc. 116 (1994) 4623
-
(1994)
J. Am. Chem. Soc.
, vol.116
, pp. 4623
-
-
Bercaw, J.E.1
Shapiro, P.J.2
Cotter, D.3
Schaefer, W.P.4
Labinger, J.A.5
-
21
-
-
0034250210
-
-
Bambirra S., Brandsma M.J.R., Brussee E.A.C., Meetsma A., Hessen B., and Teuben J.H. Organometallics 19 (2000) 3197
-
(2000)
Organometallics
, vol.19
, pp. 3197
-
-
Bambirra, S.1
Brandsma, M.J.R.2
Brussee, E.A.C.3
Meetsma, A.4
Hessen, B.5
Teuben, J.H.6
-
24
-
-
26444563321
-
-
Ma L.P., Zhang J., Cai R.F., Chen Z.X., Weng L.H., and Zhou X.G. J. Organomet. Chem. 690 (2005) 4926
-
(2005)
J. Organomet. Chem.
, vol.690
, pp. 4926
-
-
Ma, L.P.1
Zhang, J.2
Cai, R.F.3
Chen, Z.X.4
Weng, L.H.5
Zhou, X.G.6
-
28
-
-
33748792535
-
-
Ma L.P., Zhang J., Zhang Z.Z., Cai R.F., Chen Z.X., and Zhou X.G. Organometallics 25 (2006) 4571
-
(2006)
Organometallics
, vol.25
, pp. 4571
-
-
Ma, L.P.1
Zhang, J.2
Zhang, Z.Z.3
Cai, R.F.4
Chen, Z.X.5
Zhou, X.G.6
-
29
-
-
14544298297
-
-
Zhang J., Ma L.P., Cai R.F., Weng L.H., and Zhou X.G. Organometallics 24 (2005) 738
-
(2005)
Organometallics
, vol.24
, pp. 738
-
-
Zhang, J.1
Ma, L.P.2
Cai, R.F.3
Weng, L.H.4
Zhou, X.G.5
-
30
-
-
85034362371
-
-
Ma L.P., Zhang J., Cai R.F., Chen Z.X., and Zhou X.G. Dalton Trans. (2007) 2718
-
(2007)
Dalton Trans.
, pp. 2718
-
-
Ma, L.P.1
Zhang, J.2
Cai, R.F.3
Chen, Z.X.4
Zhou, X.G.5
-
31
-
-
35348853510
-
-
note
-
3Yb (0.464 g, 1.26 mmol) at room temperature. The solution slowly turned from dark green to orange red over several minutes. After stirred for overnight, the reaction solution was concentrated to ca. 5 mL by reduced pressure. Orange crystals of 1 suitable for X-ray diffraction analysis were obtained after several days at -20 °C. Yield: 0.556 g (88 %).
-
-
-
-
33
-
-
0003479179
-
-
Mori A., Cohen B.D., and Lowenthal A. (Eds), Plenum Press, New York
-
In: Mori A., Cohen B.D., and Lowenthal A. (Eds). Guanidines: Historical, Biological, Biochemical and Clinical Aspects of the Natually Occurring Guanidino Compounds (1985), Plenum Press, New York
-
(1985)
Guanidines: Historical, Biological, Biochemical and Clinical Aspects of the Natually Occurring Guanidino Compounds
-
-
-
40
-
-
35348861108
-
-
note
-
-1; MS (70 eV): m/z (%): 493 (22) [M].
-
-
-
-
42
-
-
0002094744
-
-
Zhang J., Ruan R.Y., Shao Z.H., Cai R.F., Weng L.H., and Zhou X.G. Organometallics 21 (2002) 1420
-
(2002)
Organometallics
, vol.21
, pp. 1420
-
-
Zhang, J.1
Ruan, R.Y.2
Shao, Z.H.3
Cai, R.F.4
Weng, L.H.5
Zhou, X.G.6
-
43
-
-
35348870145
-
-
note
-
2 = 0.1003 for 3634 observed reflections with I > 2σ (I).
-
-
-
-
45
-
-
0003998388
-
-
Lide D.R. (Ed), CRC press, Boca. Raton
-
In: Lide D.R. (Ed). Handbook of Chemistry and Physics (1996), CRC press, Boca. Raton
-
(1996)
Handbook of Chemistry and Physics
-
-
-
48
-
-
0001977702
-
-
Holton J., Lappert M.F., Ballard D.R., Pearce R., Atwood J.L., and Hunter W.E. J. Chem. Soc. Dalton trans. (1979) 54
-
(1979)
J. Chem. Soc. Dalton trans.
, pp. 54
-
-
Holton, J.1
Lappert, M.F.2
Ballard, D.R.3
Pearce, R.4
Atwood, J.L.5
Hunter, W.E.6
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