-
3
-
-
85021008855
-
-
US patent 3600473
-
J. D. Surmantis, US patent 3600473, 1971
-
(1971)
-
-
Surmantis, J.D.1
-
7
-
-
73549124422
-
-
C. J. O'Brien, J. L. Tellez, Z. S. Nixon, L. J. Kang, A. L. Carter, S. R. Kunkel, K. C. Przeworski, G. A. Chass, Angew. Chem. 2009, 121, 6968-6971
-
(2009)
Angew. Chem.
, vol.121
, pp. 6968-6971
-
-
O'Brien, C.J.1
Tellez, J.L.2
Nixon, Z.S.3
Kang, L.J.4
Carter, A.L.5
Kunkel, S.R.6
Przeworski, K.C.7
Chass, G.A.8
-
8
-
-
69649084793
-
-
Angew. Chem. Int. Ed. 2009, 48, 6836-6839
-
(2009)
Angew. Chem. Int. Ed.
, vol.48
, pp. 6836-6839
-
-
-
11
-
-
85021031067
-
-
For a general introduction, see
-
For a general introduction, see
-
-
-
-
12
-
-
84953405629
-
-
(Ed.: F. R. Hartley), Wiley, Chichester; for selected laboratory methods for reducing phosphane oxides by using the indicated reagents, see
-
J. W. Hartley, The Chemistry of Organophosphorus Compounds, Vol. 2, Phosphine Oxides, Sulphides, Selenides and Tellurides (Ed.:, F. R. Hartley,), 1992, Wiley, Chichester; for selected laboratory methods for reducing phosphane oxides by using the indicated reagents, see
-
(1992)
The Chemistry of Organophosphorus Compounds, Vol. 2, Phosphine Oxides, Sulphides, Selenides and Tellurides
-
-
Hartley, J.W.1
-
16
-
-
39349114563
-
-
[diisobutylaluminium hydride (DIBAL-H)]
-
C. A. Busacca, R. Raju, N. Grinberg, N. Haddad, P. James-Jones, H. Lee, J. C. Lorenz, A. Saha, C. H. Senanayake, J. Org. Chem. 2008, 73, 1524-1531 [diisobutylaluminium hydride (DIBAL-H)]
-
(2008)
J. Org. Chem.
, vol.73
, pp. 1524-1531
-
-
Busacca, C.A.1
Raju, R.2
Grinberg, N.3
Haddad, N.4
James-Jones, P.5
Lee, H.6
Lorenz, J.C.7
Saha, A.8
Senanayake, C.H.9
-
18
-
-
0010688587
-
-
(aminoalanes)
-
E. Cernia, G. M. Marcati, W. Marconi, N. Palladino, Inorg. Chim. Acta 1974, 11, 195-200 (aminoalanes)
-
(1974)
Inorg. Chim. Acta
, vol.11
, pp. 195-200
-
-
Cernia, E.1
Marcati, G.M.2
Marconi, W.3
Palladino, N.4
-
19
-
-
0030785756
-
-
(Schwartz' reagent)
-
M. Zablocka, B. Delest, A. Igau, A. Skowronska, J.-P. Majoral, Tetrahedron Lett. 1997, 38, 5997-6000 (Schwartz' reagent)
-
(1997)
Tetrahedron Lett.
, vol.38
, pp. 5997-6000
-
-
Zablocka, M.1
Delest, B.2
Igau, A.3
Skowronska, A.4
Majoral, J.-P.5
-
22
-
-
34347405797
-
-
(Ti(OiPr)/polymethylhydrosiloxanes)
-
M. Berthod, A. Favre-Réguillon, J. Mohamed, G. Mignani, G. Docherty, M. Lemaire, Synlett 2007, 1545-1548 (Ti(OiPr)/ polymethylhydrosiloxanes)
-
(2007)
Synlett
, pp. 1545-1548
-
-
Berthod, M.1
Favre-Réguillon, A.2
Mohamed, J.3
Mignani, G.4
Docherty, G.5
Lemaire, M.6
-
23
-
-
45949119640
-
-
4/electrochemically); for selected patented methods for reducing phosphane oxides directly, i.e. without transformation into dichlorophosphoranes, see
-
4/electrochemically); for selected patented methods for reducing phosphane oxides directly, i.e. without transformation into dichlorophosphoranes, see
-
(1987)
Tetrahedron Lett.
, vol.28
, pp. 5821-5822
-
-
Lecat, J.L.1
Devaud, M.2
-
25
-
-
83455184203
-
-
German Patent 3523320, (paraffin oil/activated charcoal)
-
T. Dockner, German Patent 3523320, 1985 (paraffin oil/activated charcoal)
-
(1985)
-
-
Dockner, T.1
-
26
-
-
85021004169
-
-
US patent 4507503, (trialkyalane/trialkylborane)
-
F. Frey, J. Y. Lee, US patent 4507503, 1983 (trialkyalane/trialkylborane)
-
(1983)
-
-
Frey, F.1
Lee, J.Y.2
-
27
-
-
85021042837
-
-
Ref. [2] (DIBAL-H)
-
Ref. [2] (DIBAL-H).
-
-
-
-
29
-
-
83455168128
-
-
German Patent 954247
-
G. Wittig, H. Pommer, German Patent 954247, 1956.
-
(1956)
-
-
Wittig, G.1
Pommer, H.2
-
30
-
-
0342904136
-
-
K. Akiba, K. Okada, K. Ohkata, Tetrahedron Lett. 1986, 27, 5221-5224
-
(1986)
Tetrahedron Lett.
, vol.27
, pp. 5221-5224
-
-
Akiba, K.1
Okada, K.2
Ohkata, K.3
-
32
-
-
0035413396
-
-
M. V. Kazantseva, B. V. Timokhin, A. V. Rokhin, D. G. Blazhev, A. I. Golubin, Y. V. Rybakova, Russ. J. Gen. Chem. 2001, 71, 1233-1235.
-
(2001)
Russ. J. Gen. Chem.
, vol.71
, pp. 1233-1235
-
-
Kazantseva, M.V.1
Timokhin, B.V.2
Rokhin, A.V.3
Blazhev, D.G.4
Golubin, A.I.5
Rybakova, Y.V.6
-
33
-
-
0008683075
-
-
G. Märkl, D. E. Fischer, H. Olbrich, Tetrahedron Lett. 1970, 11, 645-648
-
(1970)
Tetrahedron Lett.
, vol.11
, pp. 645-648
-
-
Märkl, G.1
Fischer, D.E.2
Olbrich, H.3
-
34
-
-
83455184204
-
-
German Patent 1259883
-
J. G. Natoli, German Patent 1259883, 1965.
-
(1965)
-
-
Natoli, J.G.1
-
36
-
-
72149097599
-
-
T. Yano, M. Kuroboshi, H. Tanaka, Tetrahedron Lett. 2010, 51, 698-701
-
(2010)
Tetrahedron Lett.
, vol.51
, pp. 698-701
-
-
Yano, T.1
Kuroboshi, M.2
Tanaka, H.3
-
37
-
-
77749280616
-
-
T. Yano, M. Hoshino, M. Kuroboshi, H. Tanaka, Synlett 2010, 801-803.
-
(2010)
Synlett
, pp. 801-803
-
-
Yano, T.1
Hoshino, M.2
Kuroboshi, M.3
Tanaka, H.4
-
38
-
-
0011835383
-
-
this transformation is also relevant for industrial processes; the reduction of phosphane oxides to phosphanes is commonly achieved by transformation to the significantly more reactive dichlorophosphoranes and subsequent reduction, e.g.: ref. [5m]
-
G. Wunsch, K. Wintersberger, H. Geierhaas, Z. Anorg. Allg. Chem. 1969, 369, 33-37; this transformation is also relevant for industrial processes; the reduction of phosphane oxides to phosphanes is commonly achieved by transformation to the significantly more reactive dichlorophosphoranes and subsequent reduction, e.g.: ref. [5m]
-
(1969)
Z. Anorg. Allg. Chem.
, vol.369
, pp. 33-37
-
-
Wunsch, G.1
Wintersberger, K.2
Geierhaas, H.3
-
40
-
-
79951856755
-
-
H. Tanaka, T. Yano, K. Kobayashi, S. Kamenoue, M. Kuroboshi, H. Kawakubo, Synlett 2011, 582-584.
-
(2011)
Synlett
, pp. 582-584
-
-
Tanaka, H.1
Yano, T.2
Kobayashi, K.3
Kamenoue, S.4
Kuroboshi, M.5
Kawakubo, H.6
-
42
-
-
0000680344
-
-
C. C. Santini, J. Fischer, F. Mathey, A. Mitschler, J. Am. Chem. Soc. 1980, 102, 5809-5815.
-
(1980)
J. Am. Chem. Soc.
, vol.102
, pp. 5809-5815
-
-
Santini, C.C.1
Fischer, J.2
Mathey, F.3
Mitschler, A.4
-
43
-
-
37049083255
-
-
A. M. Z. Slawin, D. J. Williams, P. T. Wood, J. D. Woollins, J. Chem. Soc. Chem. Commun. 1987, 1741.
-
(1987)
J. Chem. Soc. Chem. Commun.
, pp. 1741
-
-
Slawin, A.M.Z.1
Williams, D.J.2
Wood, P.T.3
Woollins, J.D.4
-
45
-
-
0000827464
-
-
T. W. Campbell, J. J. Monagle, V. S. Foldi, J. Am. Chem. Soc. 1962, 84, 3673-3677
-
(1962)
J. Am. Chem. Soc.
, vol.84
, pp. 3673-3677
-
-
Campbell, T.W.1
Monagle, J.J.2
Foldi, V.S.3
-
46
-
-
0009658930
-
-
J. J. Monagle, T. W. Campbell, H. F. McShane, Jr., J. Am. Chem. Soc. 1962, 84, 4288-4295.
-
(1962)
J. Am. Chem. Soc.
, vol.84
, pp. 4288-4295
-
-
Monagle, J.J.1
Campbell, T.W.2
Mcshane Jr., H.F.3
-
47
-
-
34250483833
-
-
H. Hoffmann, H. Förster, G. Tor-Poghossian, Monatsh. Chem. 1969, 100, 311-315.
-
(1969)
Monatsh. Chem.
, vol.100
, pp. 311-315
-
-
Hoffmann, H.1
Förster, H.2
Tor-Poghossian, G.3
-
49
-
-
83455168125
-
-
J. J. Weigand, K.-O. Feldmann, A. K. C. Echterhoff, A. W. Ehlers, K. Lammertsma, Angew. Chem. 2010, 122, 6314-6317
-
(2010)
Angew. Chem.
, vol.122
, pp. 6314-6317
-
-
Weigand, J.J.1
Feldmann, K.-O.2
Echterhoff, A.K.C.3
Ehlers, A.W.4
Lammertsma, K.5
-
50
-
-
77956041260
-
-
Angew. Chem. Int. Ed. 2010, 49, 6178-6181.
-
(2010)
Angew. Chem. Int. Ed.
, vol.49
, pp. 6178-6181
-
-
-
51
-
-
85021017629
-
-
4
-
4.
-
-
-
-
52
-
-
85021034704
-
-
2 at 300 K; varying chemical shifts have been reported for 2a in the literature, for example
-
2 at 300 K; varying chemical shifts have been reported for 2a in the literature, for example
-
-
-
-
53
-
-
33646192747
-
-
δ=23.7 ppm (in CDCl3)
-
δ=23.7 ppm (in CDCl3):, H. Rao, Y. Jin, H. Fu, Y. Jiang, Y. Zhao, Chem. Eur. J. 2006, 12, 3636-3646
-
(2006)
Chem. Eur. J.
, vol.12
, pp. 3636-3646
-
-
Rao, H.1
Jin, Y.2
Fu, H.3
Jiang, Y.4
Zhao, Y.5
-
54
-
-
65249087840
-
-
δ=29.8 ppm (in CDCl3)
-
δ=29.8 ppm (in CDCl3):, F.-H. Hu, L.-S. Wang, S.-F. Cai, J. Chem. Eng. Data 2009, 54, 1382-1384.
-
(2009)
J. Chem. Eng. Data
, vol.54
, pp. 1382-1384
-
-
Hu, F.-H.1
Wang, L.-S.2
Cai, S.-F.3
-
55
-
-
0039950516
-
-
J. Grebe, G. K. Harms, F. Weller, K. Dehnicke, Z. Anorg. Allg. Chem. 1995, 621, 1489-1495.
-
(1995)
Z. Anorg. Allg. Chem.
, vol.621
, pp. 1489-1495
-
-
Grebe, J.1
Harms, G.K.2
Weller, F.3
Dehnicke, K.4
-
56
-
-
0025999307
-
-
E. E. Nifantyev, M. K. Gratchev, S. Y. Burmistrov, L. K. Vasyanina, M. Y. Antipin, Y. T. Struchkov, Tetrahedron 1991, 47, 9839-9860.
-
(1991)
Tetrahedron
, vol.47
, pp. 9839-9860
-
-
Nifantyev, E.E.1
Gratchev, M.K.2
Burmistrov, S.Y.3
Vasyanina, L.K.4
Antipin, M.Y.5
Struchkov, Y.T.6
-
57
-
-
54049110430
-
-
I. M. Dixon, E. Lebon, G. Loustau, P. Sutra, L. Vendier, A. Igau, A. Juris, Dalton Trans. 2008, 5627-5635.
-
(2008)
Dalton Trans.
, pp. 5627-5635
-
-
Dixon, I.M.1
Lebon, E.2
Loustau, G.3
Sutra, P.4
Vendier, L.5
Igau, A.6
Juris, A.7
-
58
-
-
36048945418
-
-
J. J. Weigand, N. Burford, A. Decken, A. Schulz, Eur. J. Inorg. Chem. 2007, 4868-4872.
-
(2007)
Eur. J. Inorg. Chem.
, pp. 4868-4872
-
-
Weigand, J.J.1
Burford, N.2
Decken, A.3
Schulz, A.4
-
59
-
-
0037875345
-
-
S. Fischer, J. Hoyano, L. K. Peterson, Can. J. Chem. 1976, 54, 2710.
-
(1976)
Can. J. Chem.
, vol.54
, pp. 2710
-
-
Fischer, S.1
Hoyano, J.2
Peterson, L.K.3
-
60
-
-
85021029562
-
-
See the Supporting Information for further details
-
See the Supporting Information for further details.
-
-
-
-
61
-
-
11244333240
-
-
N. Burford, D. E. Herbert, P. J. Ragogna, R. McDonald, M. J. Ferguson, J. Am. Chem. Soc. 2004, 126, 17067
-
(2004)
J. Am. Chem. Soc.
, vol.126
, pp. 17067
-
-
Burford, N.1
Herbert, D.E.2
Ragogna, P.J.3
McDonald, R.4
Ferguson, M.J.5
-
62
-
-
0344875180
-
-
N. Burford, P. J. Ragogna, R. McDonald, M. J. Ferguson, J. Am. Chem. Soc. 2003, 125, 14404-14407.
-
(2003)
J. Am. Chem. Soc.
, vol.125
, pp. 14404-14407
-
-
Burford, N.1
Ragogna, P.J.2
McDonald, R.3
Ferguson, M.J.4
-
63
-
-
85021004167
-
-
All calculations were performed at the B3LYP/6-311G(2d) level of theory by using Gaussian 09. See the Supporting Information for further details and full citation
-
All calculations were performed at the B3LYP/6-311G(2d) level of theory by using Gaussian 09. See the Supporting Information for further details and full citation.
-
-
-
-
64
-
-
85020993079
-
-
2. However, the absolute value is strongly dependent on a solvate model and we refrain here from a detailed calculation
-
2. However, the absolute value is strongly dependent on a solvate model and we refrain here from a detailed calculation.
-
-
-
-
65
-
-
85020973093
-
-
2+, calculated by using NBO Version 3.1, developed by E. D. Glendening, A. E. Reed, J. E. Carpenter, and F. Weinhold
-
2+, calculated by using NBO Version 3.1, developed by E. D. Glendening, A. E. Reed, J. E. Carpenter, and F. Weinhold
-
-
-
-
66
-
-
0011083499
-
-
A. E. Reed, L. A. Curtiss, F. Weinhold, Chem. Rev. 1988, 88, 899.
-
(1988)
Chem. Rev.
, vol.88
, pp. 899
-
-
Reed, A.E.1
Curtiss, L.A.2
Weinhold, F.3
-
67
-
-
84855226367
-
-
4 typically gives yields of 60-80 %; (Ed.: F. R. Hartley), Wiley, Chichester, p.
-
4 typically gives yields of 60-80 %; The Chemistry of Organophosphorus Compounds, Vol. 2, Phosphine Oxides, Sulphides, Selenides and Tellurides (Ed.:, F. R. Hartley,), Wiley, Chichester, 1992, p. 292.
-
(1992)
The Chemistry of Organophosphorus Compounds, Vol. 2, Phosphine Oxides, Sulphides, Selenides and Tellurides
, pp. 292
-
-
-
68
-
-
0347266400
-
-
S.-L. You, H. Razavi, J. W. Kelly, Angew. Chem. 2003, 115, 87-89
-
(2003)
Angew. Chem.
, vol.115
, pp. 87-89
-
-
You, S.-L.1
Razavi, H.2
Kelly, J.W.3
-
72
-
-
85020961539
-
-
SAINT 7.23A, Bruker AXS, Inc, Madison, Wisconsin (USA), 2006
-
SAINT 7.23A, Bruker AXS, Inc, Madison, Wisconsin (USA), 2006
-
-
-
-
73
-
-
0006156922
-
-
Inc., Madison, Wisconsin (USA)
-
G. M. Sheldrick, SADABS, Bruker AXS, Inc., Madison, Wisconsin (USA), 2004.
-
(2004)
SADABS, Bruker AXS
-
-
Sheldrick, G.M.1
-
75
-
-
84870441500
-
-
Universität Göttingen, Göttingen (Germany)
-
G. M. Sheldrick, SHELXL-97; Universität Göttingen, Göttingen (Germany), 1997.
-
(1997)
SHELXL-97
-
-
Sheldrick, G.M.1
-
76
-
-
85020964547
-
-
These data can be obtained free of charge from the Cambridge Crystallographic Data Centre at
-
These data can be obtained free of charge from the Cambridge Crystallographic Data Centre at.
-
-
-
|