-
1
-
-
30944442835
-
-
955, and references therein;
-
a) R. R. Schrock, Acc. Chem. Res. 2005, 38, 955, and references therein;
-
(2005)
Acc. Chem. Res
, vol.38
-
-
Schrock, R.R.1
-
3
-
-
0001589060
-
-
For early reviews related to the topic, see: a
-
For early reviews related to the topic, see: a) W. A. Nugent, B. L. Haymore, Coord. Chem. Rev. 1980, 31, 123;
-
(1980)
Coord. Chem. Rev
, vol.31
, pp. 123
-
-
Nugent, W.A.1
Haymore, B.L.2
-
6
-
-
33749103583
-
-
Theoretical analysis of the bonding of hydrazido ligands: a S. Kahlal, J. Saillard, J. Hamon, C. Manzur, D. Carrillo, J. Chem. Soc. Dalton Trans. 1998, 1229;
-
Theoretical analysis of the bonding of hydrazido ligands: a) S. Kahlal, J. Saillard, J. Hamon, C. Manzur, D. Carrillo, J. Chem. Soc. Dalton Trans. 1998, 1229;
-
-
-
-
7
-
-
0035113777
-
-
b) S. Kahlal, J. Saillard, J. Hamon, C. Manzur, D. Carrillo, New J. Chem. 2001, 25, 231.
-
(2001)
New J. Chem
, vol.25
, pp. 231
-
-
Kahlal, S.1
Saillard, J.2
Hamon, J.3
Manzur, C.4
Carrillo, D.5
-
8
-
-
0034806990
-
-
Hydrohydrazination: a J. S. Johnson, R. G. Bergmann, J. Am. Chem. Soc. 2001, 123, 2923;
-
Hydrohydrazination: a) J. S. Johnson, R. G. Bergmann, J. Am. Chem. Soc. 2001, 123, 2923;
-
-
-
-
9
-
-
0000931907
-
-
b) C. Cao, Y. Shi, A. L. Odom, Org. Lett. 2002, 4, 2853;
-
(2002)
Org. Lett
, vol.4
, pp. 2853
-
-
Cao, C.1
Shi, Y.2
Odom, A.L.3
-
10
-
-
1642346954
-
-
c) V. Khedkar, A. Tillack, M. Michalik, M. Beller, Tetrahedron Lett. 2004, 45, 3123;
-
(2004)
Tetrahedron Lett
, vol.45
, pp. 3123
-
-
Khedkar, V.1
Tillack, A.2
Michalik, M.3
Beller, M.4
-
12
-
-
2942585374
-
-
Hydrazination as a key step in indole syntheses: a A. Tillack, H. Jiao, I. Garcia Castro, C. G. Hartung, M. Beller, Chem. Eur. J. 2004, 10, 2409;
-
Hydrazination as a key step in indole syntheses: a) A. Tillack, H. Jiao, I. Garcia Castro, C. G. Hartung, M. Beller, Chem. Eur. J. 2004, 10, 2409;
-
-
-
-
13
-
-
27644499585
-
-
iminohydrazination: b S. Banerjee, Y. Shi, C. Cao, A. L. Odom, J. Organomet. Chem. 2005, 690, 5066;
-
iminohydrazination: b) S. Banerjee, Y. Shi, C. Cao, A. L. Odom, J. Organomet. Chem. 2005, 690, 5066;
-
-
-
-
15
-
-
0009686083
-
-
Ti hydrazides: a N. Wiberg, H.-W. Haring, G. Huttner, P. Friedrich, Chem. Ber. 1978, 111, 2708;
-
Ti hydrazides: a) N. Wiberg, H.-W. Haring, G. Huttner, P. Friedrich, Chem. Ber. 1978, 111, 2708;
-
-
-
-
16
-
-
28844440644
-
-
b) A. J. Blake, J. M. McInnes, P. Mountford, G. I. Nikonov, D. Swallow, D. J. Watkin, J. Chem. Soc. Dalton Trans. 1999, 379;
-
(1999)
J. Chem. Soc. Dalton Trans
, pp. 379
-
-
Blake, A.J.1
McInnes, J.M.2
Mountford, P.3
Nikonov, G.I.4
Swallow, D.5
Watkin, D.J.6
-
18
-
-
1242314257
-
-
d) Y. Li, Y. Shi, A. L. Odom, J. Am. Chem. Soc. 2004, 126, 1794;
-
(2004)
J. Am. Chem. Soc
, vol.126
, pp. 1794
-
-
Li, Y.1
Shi, Y.2
Odom, A.L.3
-
19
-
-
28344450862
-
-
e) T. B. Parsons, N. Hazari, A. R. Cowley, J. C. Green, P. Mountford, Inorg. Chem. 2005, 44, 8442.
-
(2005)
Inorg. Chem
, vol.44
, pp. 8442
-
-
Parsons, T.B.1
Hazari, N.2
Cowley, A.R.3
Green, J.C.4
Mountford, P.5
-
20
-
-
0000386053
-
-
P. J. Walsh, M. J. Carney, R. G. Bergman, J. Am. Chem. Soc. 1991, 113, 6343.
-
(1991)
J. Am. Chem. Soc
, vol.113
, pp. 6343
-
-
Walsh, P.J.1
Carney, M.J.2
Bergman, R.G.3
-
21
-
-
0001343531
-
-
a) S. Friedrich, M. Schubart, L. H. Gade, I. J. Scowen, A. J. Edwards, M. McPartlin, Chem. Ber. 1997, 130, 1751;
-
(1997)
Chem. Ber
, vol.130
, pp. 1751
-
-
Friedrich, S.1
Schubart, M.2
Gade, L.H.3
Scowen, I.J.4
Edwards, A.J.5
McPartlin, M.6
-
22
-
-
0002300379
-
-
b) A. J. Blake, P. E. Collier, L. H. Gade, M. McPartlin, P. Mountford, M. Schubart, I. J. Scowen, Chem. Commun. 1997, 1555;
-
(1997)
Chem. Commun
, pp. 1555
-
-
Blake, A.J.1
Collier, P.E.2
Gade, L.H.3
McPartlin, M.4
Mountford, P.5
Schubart, M.6
Scowen, I.J.7
-
23
-
-
0035952115
-
-
c) A. J. Blake, P. E. Collier, L. H. Gade, P. Mountford, S. E. Pugh, M. Schubart, D. J. M. Trösch, Inorg. Chem. 2001, 40, 870;
-
(2001)
Inorg. Chem
, vol.40
, pp. 870
-
-
Blake, A.J.1
Collier, P.E.2
Gade, L.H.3
Mountford, P.4
Pugh, S.E.5
Schubart, M.6
Trösch, D.J.M.7
-
24
-
-
1842536008
-
-
d) B. D. Ward, A. Maisse-François, P. Mountford, L. H. Gade, Chem. Commun. 2004, 704;
-
(2004)
Chem. Commun
, pp. 704
-
-
Ward, B.D.1
Maisse-François, A.2
Mountford, P.3
Gade, L.H.4
-
25
-
-
36248946926
-
-
in press;
-
e) N. Vujkovic, B. D. Ward, A. Maisse-François, H. Wadepohl, P. Mountford, L. H. Gade, Organometallics 2007, in press;
-
(2007)
Organometallics
-
-
Vujkovic, N.1
Ward, B.D.2
Maisse-François, A.3
Wadepohl, H.4
Mountford, P.5
Gade, L.H.6
-
28
-
-
37049066790
-
-
Selected examples of hydrazido (1- charge) Ti complexes: a) I. A. Latham, G. J. Leigh, G. Huttner, I. Jibril, J. Chem. Soc. Dalton Trans. 1986, 385;
-
Selected examples of hydrazido (1- charge) Ti complexes: a) I. A. Latham, G. J. Leigh, G. Huttner, I. Jibril, J. Chem. Soc. Dalton Trans. 1986, 385;
-
-
-
-
29
-
-
37049080051
-
-
b) D. L. Hughes, M. Jimenez-Tenorio, G. J. Leigh, D. G. Walker, J. Chem. Soc. Dalton Trans. 1989, 2389;
-
(1989)
J. Chem. Soc. Dalton Trans
, pp. 2389
-
-
Hughes, D.L.1
Jimenez-Tenorio, M.2
Leigh, G.J.3
Walker, D.G.4
-
30
-
-
0035897437
-
-
c) S.-J. Kim, I. N. Jung, B. R. Yoo, S. Cho, J. Ko, S. H. Kim, S. O. Kang, Organometallics 2001, 20, 1501;
-
(2001)
Organometallics
, vol.20
, pp. 1501
-
-
Kim, S.-J.1
Jung, I.N.2
Yoo, B.R.3
Cho, S.4
Ko, J.5
Kim, S.H.6
Kang, S.O.7
-
31
-
-
0000102813
-
-
d) S. C. Yoon, B. A. Bae, I.-H. Sub, J. T. Park, Organometallics 1999, 18, 2049;
-
(1999)
Organometallics
, vol.18
, pp. 2049
-
-
Yoon, S.C.1
Bae, B.A.2
Sub, I.-H.3
Park, J.T.4
-
32
-
-
0001403497
-
-
e) T. Zippel, P. Amdt, A. Ohff, A. Spannenberg, R. Kempe, U. Rosenthal, Organometallics 1998, 17, 4429;
-
(1998)
Organometallics
, vol.17
, pp. 4429
-
-
Zippel, T.1
Amdt, P.2
Ohff, A.3
Spannenberg, A.4
Kempe, R.5
Rosenthal, U.6
-
33
-
-
0009851301
-
-
f) J. E. Hill, P. E. Fanwick, I. P. Rothwell, Inorg. Chem. 1991, 30, 1143;
-
(1991)
Inorg. Chem
, vol.30
, pp. 1143
-
-
Hill, J.E.1
Fanwick, P.E.2
Rothwell, I.P.3
-
34
-
-
0033860263
-
-
g) B. Goetze, J. Knizek, H. Nöth, W. Schnick, Eur. J. Inorg. Chem. 2000, 1849.
-
(2000)
Eur. J. Inorg. Chem
, pp. 1849
-
-
Goetze, B.1
Knizek, J.2
Nöth, H.3
Schnick, W.4
-
35
-
-
36248954138
-
-
000 = 1480.
-
000 = 1480.
-
-
-
-
36
-
-
36249021706
-
-
Crystal data of 3: C38H56N 6Si2Zr, monoclinic, space group P2 1/c, a, 10.2312(9, b, 12.4990(11, c, 30.880(3) Å, β, 97.632(2)°, V, 3913.9(6) Å3, Z, 4, μ, 0.376 mm-1, F 000, 1576. Reflections measured: 75 589, independent: 8979 [Rint, 0.098, index ranges -13 ≦ h ≦ 13, 16 ≦ k ≦ 0, 40 ≦ l 12, θ range 1.8 to 28.5°. Final R values [I > 2σ(I, R1, 0.0486, wR2, 0.1142, GooF, 1.033. 4: C38H 60N6Si2Zr, monoclinic, space group Cc, racemically twinned (refined fractions of the two crystallites 0.945 and 0.055, a, 11.7568(8, b, 18.3226(12, c, 18.9636(13) Å, β, 91.6860(10)°, V, 4083.3(5) Å
-
[11c] all non-hydrogen atoms anisotropic, hydrogen atoms at calculated positions (refined riding). CCDC-658106 (3), -658494 (4), -658107 (5), and -658108 (6) contain the supplementary crystallographic data for this paper. These data can be obtained free of charge from The Cambridge Crystallographic Data Centre via www.ccdc.cam.ac.uk/ data_request/cif. a) G. M. Sheldrick, SADABS-2004/1, Bruker AXS, 2004;
-
-
-
-
37
-
-
0005654841
-
-
University of Nijmegen, The Netherlands
-
b) P. T. Beurskens, G. Beurskens, R. de Gelder, S. Garcia-Granda, R. O. Gould, R. Israel, J. M. M. Smits, DIRDIF-99, University of Nijmegen, The Netherlands, 1999;
-
(1999)
DIRDIF
, pp. 99
-
-
Beurskens, P.T.1
Beurskens, G.2
de Gelder, R.3
Garcia-Granda, S.4
Gould, R.O.5
Israel, R.6
Smits, J.M.M.7
-
38
-
-
0004150157
-
-
University of Göttingen
-
c) G. M. Sheldrick, SHELXL-97, University of Göttingen, 1997.
-
(1997)
SHELXL-97
-
-
Sheldrick, G.M.1
-
39
-
-
36249004590
-
-
All of the molecular systems were optimized using X-ray diffraction data as input structures. Hybrid quantum mechanical:molecular mechanical (QM:MM, B3LYP:UFF) computational tools were used to model the complexes. The inner segment (QM: B3LYP; (C, N: 6-31 g(d, H: 6-31g; Zr: LANL2DZ, was defined by only the essential elements of the first coordination sphere. Stationary points were characterized by frequency analysis. Compound 3a was used as reference, which is ca. 20 kcal mol-1 higher in energy (in the gas phase) than compound 3. All the calculations, including orbital analysis (NBO 3.0, have been carried out using Gaussian 03 program package, 12a] A detailed description of the methods is provided in the supporting info. a) Gaussian 03, Revision B.03, M. J. Frisch, et al, see the Supporting Information
-
[12a] A detailed description of the methods is provided in the supporting info. a) Gaussian 03, Revision B.03, M. J. Frisch, et al., see the Supporting Information.
-
-
-
-
40
-
-
0000061312
-
-
a) T. E. Glassman, M. G. Vale, R. R. Schrock, J. Am. Chem. Soc. 1992, 114, 8098;
-
(1992)
J. Am. Chem. Soc
, vol.114
, pp. 8098
-
-
Glassman, T.E.1
Vale, M.G.2
Schrock, R.R.3
-
42
-
-
36249025004
-
-
A substituent-free N atom bonded to a metal atom is normally referred to as a nitrido ligand. However, these ligands are to be understood as formally trianionic and triply bonded to the metal. This situation is not the case for the hypothetical Zr-N species referred to in this discussion. This species has different bonding characteristics, and the required formal oxidation state of the metal center in the case of its formulation as a nitride (+ VI) is not accessible. For reviews of the chemistry of nitride complexes, see: a) K. Dehnicke, J. Strähle, Angew. Chem. 1981, 93, 451;
-
A substituent-free N atom bonded to a metal atom is normally referred to as a "nitrido ligand". However, these ligands are to be understood as formally trianionic and triply bonded to the metal. This situation is not the case for the hypothetical Zr-N species referred to in this discussion. This species has different bonding characteristics, and the required formal oxidation state of the metal center in the case of its formulation as a nitride (+ VI) is not accessible. For reviews of the chemistry of nitride complexes, see: a) K. Dehnicke, J. Strähle, Angew. Chem. 1981, 93, 451;
-
-
-
-
45
-
-
33751140722
-
-
955; as well as
-
Angew. Chem. Int. Ed. Engl. 1992, 31, 955; as well as ref. [19d].
-
(1992)
Angew. Chem. Int. Ed. Engl
, vol.31
-
-
-
46
-
-
32244439080
-
-
a) Y.-J. Kim, X. Chang, J.-T. Han, M. S. Lim, S. W. Lee, Dalton Trans. 2004, 3699;
-
(2004)
Dalton Trans
, pp. 3699
-
-
Kim, Y.-J.1
Chang, X.2
Han, J.-T.3
Lim, M.S.4
Lee, S.W.5
-
47
-
-
0037151950
-
-
b) Y.-J. Kim, Y.-S. Joo, J.-T. Han, W. S. Han, S. W. Lee, J. Chem. Soc. Dalton Trans. 2002, 3611;
-
(2002)
J. Chem. Soc. Dalton Trans
, pp. 3611
-
-
Kim, Y.-J.1
Joo, Y.-S.2
Han, J.-T.3
Han, W.S.4
Lee, S.W.5
-
48
-
-
0036007653
-
-
c) Y.-J. Kim, Y.-S. Kwak, Y.-S. Joo, S. W. Lee, J. Chem. Soc. Dalton Trans. 2001, 144;
-
(2001)
J. Chem. Soc. Dalton Trans
, pp. 144
-
-
Kim, Y.-J.1
Kwak, Y.-S.2
Joo, Y.-S.3
Lee, S.W.4
-
49
-
-
0000032868
-
-
d) Y.-J. Kim, Y.-S. Kwak, S. W. Lee, J. Organomet. Chem. 2000, 603, 152.
-
(2000)
J. Organomet. Chem
, vol.603
, pp. 152
-
-
Kim, Y.-J.1
Kwak, Y.-S.2
Lee, S.W.3
-
50
-
-
85178819503
-
-
Ti carbodimides have been synthesized by other routes: e H. Plenio, H. W. Roesky, Z. Naturforsch. B 1989, 44, 94;
-
Ti carbodimides have been synthesized by other routes: e) H. Plenio, H. W. Roesky, Z. Naturforsch. B 1989, 44, 94;
-
-
-
-
51
-
-
0001166827
-
-
f) G. Veneziani, S. Shimada, M. Tanaka, Organometallics 1998, 17, 2926.
-
(1998)
Organometallics
, vol.17
, pp. 2926
-
-
Veneziani, G.1
Shimada, S.2
Tanaka, M.3
-
52
-
-
0032496935
-
-
T. J. Crevier, S. Lovell, J. M. Mayer, A. L. Rheingold, I. A. Guzei, J. Am. Chem. Soc. 1998, 120, 6607.
-
(1998)
J. Am. Chem. Soc
, vol.120
, pp. 6607
-
-
Crevier, T.J.1
Lovell, S.2
Mayer, J.M.3
Rheingold, A.L.4
Guzei, I.A.5
-
53
-
-
16244389346
-
-
Recent examples of the use of propylene sulfide a S-atom transfer reagent: a S. Blum, V. A. Rivera, R. T. Ruck, F. E. Michael, R. G. Bergman, Organometallics 2005, 24, 1647;
-
Recent examples of the use of propylene sulfide a S-atom transfer reagent: a) S. Blum, V. A. Rivera, R. T. Ruck, F. E. Michael, R. G. Bergman, Organometallics 2005, 24, 1647;
-
-
-
-
54
-
-
0035977760
-
-
S. M. Mullins, A. P. Duncan, R. G. Bergman, J. Arnold, Inorg. Chem. 2001, 40, 6952.
-
(2001)
Inorg. Chem
, vol.40
, pp. 6952
-
-
Mullins, S.M.1
Duncan, A.P.2
Bergman, R.G.3
Arnold, J.4
-
55
-
-
0000166746
-
-
Examples of the use of triphenylphosphine selenide as a Se-atom transfer reagent: a S. M. Stuczynski, Y.-U. Kwon, M. L. Steigerwald, J. Organomet. Chem. 1993, 449, 167;
-
Examples of the use of triphenylphosphine selenide as a Se-atom transfer reagent: a) S. M. Stuczynski, Y.-U. Kwon, M. L. Steigerwald, J. Organomet. Chem. 1993, 449, 167;
-
-
-
-
56
-
-
0001322128
-
-
b) M. L. Steigerwald, T. Siegrist, E. M. Gyorgy, B. Hessen, Y.-U. Kwon, S. M. Tanzler, Inorg. Chem. 1994, 33, 3389;
-
(1994)
Inorg. Chem
, vol.33
, pp. 3389
-
-
Steigerwald, M.L.1
Siegrist, T.2
Gyorgy, E.M.3
Hessen, B.4
Kwon, Y.-U.5
Tanzler, S.M.6
-
57
-
-
0042889499
-
-
R. D. Adams, O.-Sung Kwon, S. Sanyal, J. Organomet. Chem. 2003, 681, 258;
-
c) R. D. Adams, O.-Sung Kwon, S. Sanyal, J. Organomet. Chem. 2003, 681, 258;
-
-
-
-
58
-
-
0036025592
-
-
d) D. Belletti, D. Cauzzi, C. Graiff, A. Minarelli, R. Pattacini, G. Predieri, A. Tiripicchio, J. Chem. Soc. Dalton Trans. 2002, 3160.
-
(2002)
J. Chem. Soc. Dalton Trans
, pp. 3160
-
-
Belletti, D.1
Cauzzi, D.2
Graiff, C.3
Minarelli, A.4
Pattacini, R.5
Predieri, G.6
Tiripicchio, A.7
-
61
-
-
0006438444
-
-
Ed, H. W. Roesky, Elesevier, Amsterdam
-
c) H. W. Roesky in Rings, Clusters and Polymers of Main Group and Transition Elements (Ed.: H. W. Roesky), Elesevier, Amsterdam, 1989, p. 369;
-
(1989)
Rings, Clusters and Polymers of Main Group and Transition Elements
, pp. 369
-
-
Roesky, H.W.1
-
62
-
-
57249084545
-
-
d) K. Dehnicke, F. Weller, J. Strähle, Chem. Soc. Rev. 2001, 30, 125;
-
(2001)
Chem. Soc. Rev
, vol.30
, pp. 125
-
-
Dehnicke, K.1
Weller, F.2
Strähle, J.3
-
64
-
-
0035813854
-
-
Angew. Chem. Int. Ed. 2001, 40, 3960.
-
(2001)
Chem. Int. Ed
, vol.40
, pp. 3960
-
-
Angew1
-
65
-
-
0036555563
-
-
a) J. Mason, L. F. Larkworthy, E. A. Moore, Chem. Rev. 2002, 102, 913;
-
(2002)
Chem. Rev
, vol.102
, pp. 913
-
-
Mason, J.1
Larkworthy, L.F.2
Moore, E.A.3
-
67
-
-
85178834822
-
-
NSN; a K. Hösler, F. Weller, K. Dehnicke, Z. Naturforsch. B 1989, 44, 1325;
-
NSN; a) K. Hösler, F. Weller, K. Dehnicke, Z. Naturforsch. B 1989, 44, 1325;
-
-
-
-
69
-
-
84866569066
-
-
A. Dietrich, B. Neumüller, K. Dehnicke, Z. Anorg. Allg. Chem. 2002, 628, 243.
-
c) A. Dietrich, B. Neumüller, K. Dehnicke, Z. Anorg. Allg. Chem. 2002, 628, 243.
-
-
-
-
70
-
-
85178790865
-
-
2- fragment coordinated to metals, nor - to our knowledge - any characterizing data on the unit itself. Organic selenodiimides have been reported: a M. Herberhold, W. Jellen, Z. Naturforsch. B 1986, 41, 144;
-
2- fragment coordinated to metals, nor - to our knowledge - any characterizing data on the unit itself. Organic selenodiimides have been reported: a) M. Herberhold, W. Jellen, Z. Naturforsch. B 1986, 41, 144;
-
-
-
-
71
-
-
9144229660
-
-
b) T. Maaninen, H. M. Tuononen, K. Kosunen, R. Oilunkaniemi, J. Hiitola, R. Laitinen, T. Chivers, Z. Anorg. Allg. Chem. 2004, 630, 1947;
-
(2004)
Z. Anorg. Allg. Chem
, vol.630
, pp. 1947
-
-
Maaninen, T.1
Tuononen, H.M.2
Kosunen, K.3
Oilunkaniemi, R.4
Hiitola, J.5
Laitinen, R.6
Chivers, T.7
-
72
-
-
0036969866
-
-
an X-ray diffraction study of AdNSeNAd: c T. Maaninen, R. Laitinen, T. Chivers, Chem. Commun. 2002, 1812;
-
an X-ray diffraction study of AdNSeNAd: c) T. Maaninen, R. Laitinen, T. Chivers, Chem. Commun. 2002, 1812;
-
-
-
-
73
-
-
37049086300
-
-
2Se, see: d) J. Gindl, M. Börgvinsson, H. W. Roesky, C. Freire-Erdbrügger, G. M. Sheldrick, J. Chem. Soc. Dalton Trans. 1993, 811;
-
2Se, see: d) J. Gindl, M. Börgvinsson, H. W. Roesky, C. Freire-Erdbrügger, G. M. Sheldrick, J. Chem. Soc. Dalton Trans. 1993, 811;
-
-
-
-
74
-
-
36249024465
-
-
2N2} cycle in Group 10 metal complexes: e P. F. Kelly, A. M. Z. Slawin, Angew. Chem. 1995, 107, 1903;
-
2N2} cycle in Group 10 metal complexes: e) P. F. Kelly, A. M. Z. Slawin, Angew. Chem. 1995, 107, 1903;
-
-
-
-
77
-
-
0012905360
-
-
a) D. Leusser, B. Walfort, D. Stalke, Angew. Chem. 2002, 114, 2183;
-
(2002)
Angew. Chem
, vol.114
, pp. 2183
-
-
Leusser, D.1
Walfort, B.2
Stalke, D.3
-
78
-
-
0037124797
-
-
Angew. Chem. Int. Ed. 2002, 41, 2079;
-
(2002)
Chem. Int. Ed
, vol.41
, pp. 2079
-
-
Angew1
-
79
-
-
1242336827
-
-
b) D. Leusser, J. Kenn, N. Kocher, B. Engels, D. Stalke, J. Am. Chem. Soc. 2004, 126, 1781.
-
(2004)
J. Am. Chem. Soc
, vol.126
, pp. 1781
-
-
Leusser, D.1
Kenn, J.2
Kocher, N.3
Engels, B.4
Stalke, D.5
-
80
-
-
37549021889
-
-
Note added in proof: While this work was in press the N-N fragmentation of a Ti hydrazide has been reported: J. D. Selby, C. D. Manley, M. Feliz, A. D. Schwarz, E. Clot, P. Mountford, Chem. Commun. 2007, DOI: 10.1039/b711941k.
-
Note added in proof: While this work was in press the N-N fragmentation of a Ti hydrazide has been reported: J. D. Selby, C. D. Manley, M. Feliz, A. D. Schwarz, E. Clot, P. Mountford, Chem. Commun. 2007, DOI: 10.1039/b711941k.
-
-
-
|