-
1
-
-
0003400107
-
-
Wiley, New York
-
R. Noyori in Asymmetric Catalysis in Organic Synthesis, Wiley, New York, 1994; Catalytic Asymmetric Synthesis (Ed.: I. Ojima), Wiley-VCH, Weinheim, 2000; Comprehensive Asymmetric Catalysis (Eds.: E. N. Jacobson, A. Pfaltz, H. Yamamoto), Springer, Heidelberg, 1999; M. McCarthy, P. J. Guiry, Tetrahedron 2001, 57, 3809-3844.
-
(1994)
Asymmetric Catalysis in Organic Synthesis
-
-
Noyori, R.1
-
2
-
-
0003544583
-
-
(Ed.: I. Ojima), Wiley-VCH, Weinheim
-
R. Noyori in Asymmetric Catalysis in Organic Synthesis, Wiley, New York, 1994; Catalytic Asymmetric Synthesis (Ed.: I. Ojima), Wiley-VCH, Weinheim, 2000; Comprehensive Asymmetric Catalysis (Eds.: E. N. Jacobson, A. Pfaltz, H. Yamamoto), Springer, Heidelberg, 1999; M. McCarthy, P. J. Guiry, Tetrahedron 2001, 57, 3809-3844.
-
(2000)
Catalytic Asymmetric Synthesis
-
-
-
3
-
-
0003445429
-
-
(Eds.: E. N. Jacobson, A. Pfaltz, H. Yamamoto), Springer, Heidelberg
-
R. Noyori in Asymmetric Catalysis in Organic Synthesis, Wiley, New York, 1994; Catalytic Asymmetric Synthesis (Ed.: I. Ojima), Wiley-VCH, Weinheim, 2000; Comprehensive Asymmetric Catalysis (Eds.: E. N. Jacobson, A. Pfaltz, H. Yamamoto), Springer, Heidelberg, 1999; M. McCarthy, P. J. Guiry, Tetrahedron 2001, 57, 3809-3844.
-
(1999)
Comprehensive Asymmetric Catalysis
-
-
-
4
-
-
0035971715
-
-
R. Noyori in Asymmetric Catalysis in Organic Synthesis, Wiley, New York, 1994; Catalytic Asymmetric Synthesis (Ed.: I. Ojima), Wiley-VCH, Weinheim, 2000; Comprehensive Asymmetric Catalysis (Eds.: E. N. Jacobson, A. Pfaltz, H. Yamamoto), Springer, Heidelberg, 1999; M. McCarthy, P. J. Guiry, Tetrahedron 2001, 57, 3809-3844.
-
(2001)
Tetrahedron
, vol.57
, pp. 3809-3844
-
-
McCarthy, M.1
Guiry, P.J.2
-
5
-
-
0042880932
-
-
P. Kočovský, Š. Vyskočil, M. Smrčina, Chem. Rev. 2003, 103, 3213-3245; for a comprehensive review on N,P ligands in general, see: P. J. Guiry, C. P. Saunders, Adv. Synth. Catal. 2004, 346, 497-537.
-
(2003)
Chem. Rev.
, vol.103
, pp. 3213-3245
-
-
Kočovský, P.1
Vyskočil, Š.2
Smrčina, M.3
-
6
-
-
2542451759
-
-
P. Kočovský, Š. Vyskočil, M. Smrčina, Chem. Rev. 2003, 103, 3213-3245; for a comprehensive review on N,P ligands in general, see: P. J. Guiry, C. P. Saunders, Adv. Synth. Catal. 2004, 346, 497-537.
-
(2004)
Adv. Synth. Catal.
, vol.346
, pp. 497-537
-
-
Guiry, P.J.1
Saunders, C.P.2
-
7
-
-
0033846922
-
-
K. Sumi, T. Ikariya, R. Noyori, Can. J. Chem. 2000, 78, 697-703.
-
(2000)
Can. J. Chem.
, vol.78
, pp. 697-703
-
-
Sumi, K.1
Ikariya, T.2
Noyori, R.3
-
9
-
-
0002017795
-
-
a) Š. Vyskočil, M. Smrčina, V. Hanuš, M. Polášek, P. Kočovský, J. Org. Chem. 1998, 63, 7738-7748;
-
(1998)
J. Org. Chem.
, vol.63
, pp. 7738-7748
-
-
Vyskočil, Š.1
Smrčina, M.2
Hanuš, V.3
Polášek, M.4
Kočovský, P.5
-
10
-
-
0032976808
-
-
b) K. Ding, Y. Wang, H. Yun, J. Liu, Y. Wu, M. Terada, Y. Okubo, K. Mikami, Chem. Eur. J. 1999, 5, 1734-1737.
-
(1999)
Chem. Eur. J.
, vol.5
, pp. 1734-1737
-
-
Ding, K.1
Wang, Y.2
Yun, H.3
Liu, J.4
Wu, Y.5
Terada, M.6
Okubo, Y.7
Mikami, K.8
-
11
-
-
0033524686
-
-
A formal synthesis of MAP-type ligands from (R)-binol can be envisioned as (R)-nobin has been prepared from (R)-binol in 6 steps (61% overall yield); see: R. A. Singer, S. L. Buchwald, Tetrahedron Lett. 1999, 40, 1095-1098.
-
(1999)
Tetrahedron Lett.
, vol.40
, pp. 1095-1098
-
-
Singer, R.A.1
Buchwald, S.L.2
-
12
-
-
0025017980
-
-
L. Kurz, G. Lee, D. Morgans, Jr., M. J. Waldyke, T. Ward, Tetrahedron Lett. 1990, 31, 6321-6324.
-
(1990)
Tetrahedron Lett.
, vol.31
, pp. 6321-6324
-
-
Kurz, L.1
Lee, G.2
Morgans Jr., D.3
Waldyke, M.J.4
Ward, T.5
-
13
-
-
0141522864
-
-
For the introduction of phosphane and phosphane oxide groups, see: I. P. Beletskaya, M. A. Kazankova, Russ. J. Org. Chem. 2002, 38, 1391-1430; for the introduction of aryl groups, see: T. Hayashi, J. W. Han, A. Takeda, J. Tang, K. Nohmi, K. Mukaide, H. Tsuji, Y. Uozumi, Adv. Synth. Catal. 2001, 343, 279-283.
-
(2002)
Russ. J. Org. Chem.
, vol.38
, pp. 1391-1430
-
-
Beletskaya, I.P.1
Kazankova, M.A.2
-
14
-
-
0001254371
-
-
For the introduction of phosphane and phosphane oxide groups, see: I. P. Beletskaya, M. A. Kazankova, Russ. J. Org. Chem. 2002, 38, 1391-1430; for the introduction of aryl groups, see: T. Hayashi, J. W. Han, A. Takeda, J. Tang, K. Nohmi, K. Mukaide, H. Tsuji, Y. Uozumi, Adv. Synth. Catal. 2001, 343, 279-283.
-
(2001)
Adv. Synth. Catal.
, vol.343
, pp. 279-283
-
-
Hayashi, T.1
Han, J.W.2
Takeda, A.3
Tang, J.4
Nohmi, K.5
Mukaide, K.6
Tsuji, H.7
Uozumi, Y.8
-
15
-
-
0038579438
-
-
X. Huang, K. W. Anderson, D. Zim, L. Jiang, A. Klapars, S. L. Buchwald, J. Am. Chem. Soc. 2003, 125, 6653-6655.
-
(2003)
J. Am. Chem. Soc.
, vol.125
, pp. 6653-6655
-
-
Huang, X.1
Anderson, K.W.2
Zim, D.3
Jiang, L.4
Klapars, A.5
Buchwald, S.L.6
-
16
-
-
0002017795
-
-
a) Š. Vyskočil, M. Smrčina, V. Hanuš, M. Polášek, P. Kočovský, J. Org. Chem. 1998, 63, 7738-7748;
-
(1998)
J. Org. Chem.
, vol.63
, pp. 7738-7748
-
-
Vyskočil, Š.1
Smrčina, M.2
Hanuš, V.3
Polášek, M.4
Kočovský, P.5
-
17
-
-
0033549049
-
-
b) A. Aranyos, D. W. Old, A. Kiyomori, J. P. Wolfe, P. Sadigishi, S. L. Buchwald, J. Am. Chem. Soc. 1999, 121, 4369-4378;
-
(1999)
J. Am. Chem. Soc.
, vol.121
, pp. 4369-4378
-
-
Aranyos, A.1
Old, D.W.2
Kiyomori, A.3
Wolfe, J.P.4
Sadigishi, P.5
Buchwald, S.L.6
-
18
-
-
0032506564
-
-
c) Š. Vyskočil, M. Smrčina, P. Koč ovský, Tetrahedron Lett. 1998, 39, 9289-9292;
-
(1998)
Tetrahedron Lett.
, vol.39
, pp. 9289-9292
-
-
Vyskočil, Š.1
Smrčina, M.2
Kočovský, P.3
-
19
-
-
0032560932
-
-
d) D. W. Old, J. P. Wolfe, S. L. Buchwald, J. Am. Chem. Soc. 1998, 120, 9722-9723.
-
(1998)
J. Am. Chem. Soc.
, vol.120
, pp. 9722-9723
-
-
Old, D.W.1
Wolfe, J.P.2
Buchwald, S.L.3
-
20
-
-
0345529047
-
-
For a recent article on Pd-catalyzed aminations starting from nonaflates, see: K. W. Anderson, M. Mendez-Perez, J. Priego, S. L. Buchwald, J. Org. Chem. 2003, 68, 9563-9573.
-
(2003)
J. Org. Chem.
, vol.68
, pp. 9563-9573
-
-
Anderson, K.W.1
Mendez-Perez, M.2
Priego, J.3
Buchwald, S.L.4
-
21
-
-
4544303109
-
-
a) O. David, W. J. N. Meester, H. Bieräugel, H. E. Schoemaker, H. Hiemstra, J. H. van Maarseveen, Angew. Chem. 2003, 115, 4509-4511; Angew. Chem. Int. Ed. 2003, 42, 4373-4375;
-
(2003)
Angew. Chem.
, vol.115
, pp. 4509-4511
-
-
David, O.1
Meester, W.J.N.2
Bieräugel, H.3
Schoemaker, H.E.4
Hiemstra, H.5
Van Maarseveen, J.H.6
-
22
-
-
0141869035
-
-
a) O. David, W. J. N. Meester, H. Bieräugel, H. E. Schoemaker, H. Hiemstra, J. H. van Maarseveen, Angew. Chem. 2003, 115, 4509-4511; Angew. Chem. Int. Ed. 2003, 42, 4373-4375;
-
(2003)
Angew. Chem. Int. Ed.
, vol.42
, pp. 4373-4375
-
-
-
23
-
-
0034677879
-
-
for the original work on Staudinger ligations, see: b) E. Saxon, C. R. Bertozzi, Science 2000, 287, 2007-2010;
-
(2000)
Science
, vol.287
, pp. 2007-2010
-
-
Saxon, E.1
Bertozzi, C.R.2
-
24
-
-
0034643993
-
-
c) E. Saxon, J. I. Armstrong, C. R. Bertozzi, Org. Lett. 2000, 2, 2141-2143;
-
(2000)
Org. Lett.
, vol.2
, pp. 2141-2143
-
-
Saxon, E.1
Armstrong, J.I.2
Bertozzi, C.R.3
-
25
-
-
0037132659
-
-
d) E. Saxon, S. J. Luchansky, H. C. Hang, C. Yu, S. C. Lee, C. R. Bertozzi, J. Am. Chem. Soc. 2002, 124, 14893-14902;
-
(2002)
J. Am. Chem. Soc.
, vol.124
, pp. 14893-14902
-
-
Saxon, E.1
Luchansky, S.J.2
Hang, H.C.3
Yu, C.4
Lee, S.C.5
Bertozzi, C.R.6
-
26
-
-
0034729576
-
-
e) B. L. Nilsson, L. L. Kiessling, R. T. Raines, Org. Lett. 2000, 2, 1939;
-
(2000)
Org. Lett.
, vol.2
, pp. 1939
-
-
Nilsson, B.L.1
Kiessling, L.L.2
Raines, R.T.3
-
27
-
-
0035843279
-
-
f) B. L. Nilsson, L. L. Kiessling, R. T. Raines, Org. Lett. 2001, 3, 9-12;
-
(2001)
Org. Lett.
, vol.3
, pp. 9-12
-
-
Nilsson, B.L.1
Kiessling, L.L.2
Raines, R.T.3
-
28
-
-
0037067343
-
-
g) M. B. Soellner, B. L. Nilsson, R. T. Raines, J. Org. Chem. 2002, 67, 4993-4996.
-
(2002)
J. Org. Chem.
, vol.67
, pp. 4993-4996
-
-
Soellner, M.B.1
Nilsson, B.L.2
Raines, R.T.3
-
29
-
-
0000363937
-
-
For reviews on the Staudinger reaction, see: a) Y. G. Gololobov, I. N. Zhmurova, L. F. Kasukhin, Tetrahedron 1981, 37, 437-472;
-
(1981)
Tetrahedron
, vol.37
, pp. 437-472
-
-
Gololobov, Y.G.1
Zhmurova, I.N.2
Kasukhin, L.F.3
-
31
-
-
0033677807
-
-
3: a) K. Hemming, M. J. Bevan, C. Loukou, S. D. Patel, D. Renaudeau, Synlett 2000, 1565-1568;
-
(2000)
Synlett
, pp. 1565-1568
-
-
Hemming, K.1
Bevan, M.J.2
Loukou, C.3
Patel, S.D.4
Renaudeau, D.5
-
33
-
-
0033600690
-
-
For the synthesis of focal-point-functionalized carbosilane dendritic wedges, see: R. van Heerbeek, P. C. J. Kamer, J. N. H. Reek, P. W. N. M. van Leeuwen, Tetrahedron Lett. 1999, 40, 7127-7130.
-
(1999)
Tetrahedron Lett.
, vol.40
, pp. 7127-7130
-
-
Van Heerbeek, R.1
Kamer, P.C.J.2
Reek, J.N.H.3
Van Leeuwen, P.W.N.M.4
-
34
-
-
0036087844
-
-
P. N. M. Botman, M. Postma, J. Fraanje, K. Goubitz, H. Schenk, J. H. van Maarseveen, H. Hiemstra, Eur. J. Org. Chem. 2002, 1952-1955.
-
(2002)
Eur. J. Org. Chem.
, pp. 1952-1955
-
-
Botman, P.N.M.1
Postma, M.2
Fraanje, J.3
Goubitz, K.4
Schenk, H.5
Van Maarseveen, J.H.6
Hiemstra, H.7
-
35
-
-
4544265766
-
-
submitted
-
P. N. M. Botman, J. Fraanje, K. Goubitz, R. Peschar, J. W. Verhoeven, J. H. van Maarseveen, H. Hiemstra, Adv. Synth. Cat., submitted.
-
Adv. Synth. Cat.
-
-
Botman, P.N.M.1
Fraanje, J.2
Goubitz, K.3
Peschar, R.4
Verhoeven, J.W.5
Van Maarseveen, J.H.6
Hiemstra, H.7
-
38
-
-
4544358887
-
-
CCDC 239743 contains the supplementary crystallographic data for this paper. These data can be obtained free of charge via www.ccdc.cam.ac.uk/conts/ retrieving.html (or from the Cambridge Crystallographic Data Centre, 12, Union Road, Cambridge CB2 1EZ, UK; fax: (+44) 1223-336-033; or deposit@ ccdc.cam.ac.uk).
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