-
1
-
-
84891580093
-
-
3 rd ed. (Ed.: I. Ojima), Wiley, Hoboken.
-
Catalytic Asymmetric Synthesis, 3 rd ed., (Ed.: I. Ojima,), Wiley, Hoboken, 2010.
-
(2010)
Catalytic Asymmetric Synthesis
-
-
-
2
-
-
53849089968
-
-
J. Steinreiber, K. Faber, H. Griengl, Chem. Eur. J. 2008, 14, 8060
-
(2008)
Chem. Eur. J.
, vol.14
, pp. 8060
-
-
Steinreiber, J.1
Faber, K.2
Griengl, H.3
-
3
-
-
0042880932
-
-
P. Kočovský, Š. Vyskočil, M. Smrčina, Chem. Rev. 2003, 103, 3213.
-
(2003)
Chem. Rev.
, vol.103
, pp. 3213
-
-
Kočovský, P.1
Vyskočil, Š.2
Smrčina, M.3
-
5
-
-
53349113487
-
-
Angew. Chem. 2008, 120, 264
-
(2008)
Angew. Chem.
, vol.120
, pp. 264
-
-
-
6
-
-
84878502378
-
-
M. T. Oliveira, D. Audisio, S. Niyomchon, N. Maulide, ChemCatChem 2013, 5, 1239.
-
(2013)
ChemCatChem
, vol.5
, pp. 1239
-
-
Oliveira, M.T.1
Audisio, D.2
Niyomchon, S.3
Maulide, N.4
-
7
-
-
35048857286
-
-
For an account on DYKAT in asymmetric allylic alkylation, see.
-
For an account on DYKAT in asymmetric allylic alkylation, see, B. M. Trost, D. R. Fandrick, Aldrichimica Acta 2007, 40, 59.
-
(2007)
Aldrichimica Acta
, vol.40
, pp. 59
-
-
Trost, B.M.1
Fandrick, D.R.2
-
8
-
-
0029837557
-
-
N. Sträter, W. N. Lipscomb, T. Klabunde, B. Krebs, Angew. Chem. Int. Ed. Engl. 1996, 35, 2024
-
(1996)
Angew. Chem. Int. Ed. Engl.
, vol.35
, pp. 2024
-
-
Sträter, N.1
Lipscomb, W.N.2
Klabunde, T.3
Krebs, B.4
-
9
-
-
0001233207
-
-
Angew. Chem. 1996, 108, 2158.
-
(1996)
Angew. Chem.
, vol.108
, pp. 2158
-
-
-
10
-
-
0030567369
-
-
M. Sawamura, M. Sudoh, Y. Ito, J. Am. Chem. Soc. 1996, 118, 3309.
-
(1996)
J. Am. Chem. Soc.
, vol.118
, pp. 3309
-
-
Sawamura, M.1
Sudoh, M.2
Ito, Y.3
-
11
-
-
84878349078
-
-
S. Krautwald, D. Sarlah, M. A. Schafroth, E. M. Carreira, Science 2013, 340, 1065
-
(2013)
Science
, vol.340
, pp. 1065
-
-
Krautwald, S.1
Sarlah, D.2
Schafroth, M.A.3
Carreira, E.M.4
-
15
-
-
84876733776
-
-
X. Huang, S. Klimczyk, L. F. Veiros, N. Maulide, Chem. Sci. 2013, 4, 1105.
-
(2013)
Chem. Sci.
, vol.4
, pp. 1105
-
-
Huang, X.1
Klimczyk, S.2
Veiros, L.F.3
Maulide, N.4
-
18
-
-
79955760094
-
-
Y. P. Xiao, X. Y. Liu, C. M. Che, Angew. Chem. Int. Ed. 2011, 50, 4937
-
(2011)
Angew. Chem. Int. Ed.
, vol.50
, pp. 4937
-
-
Xiao, Y.P.1
Liu, X.Y.2
Che, C.M.3
-
19
-
-
84939562951
-
-
Angew. Chem. 2011, 123, 5039
-
(2011)
Angew. Chem.
, vol.123
, pp. 5039
-
-
-
21
-
-
33746305736
-
-
Angew. Chem. 2006, 118, 1779
-
(2006)
Angew. Chem.
, vol.118
, pp. 1779
-
-
-
22
-
-
79951482180
-
-
N. D. Shapiro, V. Rauniyar, G. L. Hamilton, J. Wu, F. D. Toste, Nature 2011, 470, 245
-
(2011)
Nature
, vol.470
, pp. 245
-
-
Shapiro, N.D.1
Rauniyar, V.2
Hamilton, G.L.3
Wu, J.4
Toste, F.D.5
-
23
-
-
18244399612
-
-
C. Nieto-Oberhuber, S. Lõpez, A. M. Echavarren, J. Am. Chem. Soc. 2005, 127, 6178
-
(2005)
J. Am. Chem. Soc.
, vol.127
, pp. 6178
-
-
Nieto-Oberhuber, C.1
Lõpez, S.2
Echavarren, A.M.3
-
25
-
-
80052080149
-
-
Angew. Chem. 2011, 123, 936.
-
(2011)
Angew. Chem.
, vol.123
, pp. 936
-
-
-
26
-
-
84921726245
-
-
For enantioselective gold-catalyzed cyclopropanation, see.
-
For enantioselective gold-catalyzed cyclopropanation, see, D. Qian, J. Zhang, Chem. Soc. Rev. 2015, 44, 677.
-
(2015)
Chem. Soc. Rev.
, vol.44
, pp. 677
-
-
Qian, D.1
Zhang, J.2
-
27
-
-
77949418593
-
-
H. Teller, R. Flügge, R. Goddard, A. Fürstner, Angew. Chem. Int. Ed. 2010, 49, 1949
-
(2010)
Angew. Chem. Int. Ed.
, vol.49
, pp. 1949
-
-
Teller, H.1
Flügge, R.2
Goddard, R.3
Fürstner, A.4
-
28
-
-
77950260496
-
-
Angew. Chem. 2010, 122, 1993
-
(2010)
Angew. Chem.
, vol.122
, pp. 1993
-
-
-
29
-
-
84866510167
-
-
H. Teller, M. Corbet, L. Mantilli, G. Gopakumar, R. Goddard, W. Thiel, A. Fürstner, J. Am. Chem. Soc. 2012, 134, 15331.
-
(2012)
J. Am. Chem. Soc.
, vol.134
, pp. 15331
-
-
Teller, H.1
Corbet, M.2
Mantilli, L.3
Gopakumar, G.4
Goddard, R.5
Thiel, W.6
Fürstner, A.7
-
31
-
-
0000817646
-
-
Angew. Chem. 2000, 112, 4407
-
(2000)
Angew. Chem.
, vol.112
, pp. 4407
-
-
-
34
-
-
34548635326
-
-
Angew. Chem. 2007, 119, 3478
-
(2007)
Angew. Chem.
, vol.119
, pp. 3478
-
-
-
37
-
-
51049121927
-
-
Z. Li, C. Brouwer, C. He, Chem. Rev. 2008, 108, 3239
-
(2008)
Chem. Rev.
, vol.108
, pp. 3239
-
-
Li, Z.1
Brouwer, C.2
He, C.3
-
42
-
-
85000247101
-
-
Angew. Chem. 2006, 118, 4299
-
(2006)
Angew. Chem.
, vol.118
, pp. 4299
-
-
-
43
-
-
34547567515
-
-
G. L. Hamilton, E. J. Kang, M. Mba, F. D. Toste, Science 2007, 317, 496.
-
(2007)
Science
, vol.317
, pp. 496
-
-
Hamilton, G.L.1
Kang, E.J.2
Mba, M.3
Toste, F.D.4
-
44
-
-
34547413527
-
-
For a related rearrangement, see, In control experiments, we have established that allylic isomerization requires the presence of the gold catalyst and is independent of the ylide appendage. See the Supporting Information for details.
-
For a related rearrangement, see, N. Marion, R. Gealageas, S. P. Nolan, Org. Lett. 2007, 9, 2653. In control experiments, we have established that allylic isomerization requires the presence of the gold catalyst and is independent of the ylide appendage. See the Supporting Information for details.
-
(2007)
Org. Lett.
, vol.9
, pp. 2653
-
-
Marion, N.1
Gealageas, R.2
Nolan, S.P.3
-
45
-
-
84939562065
-
-
In support of this hypothesis, the enantiomeric ratio of the product remains constant throughout the entire reaction and the formed enantioenriched product does not racemize upon exposure to the reaction conditions. See the Supporting Information for details
-
In support of this hypothesis, the enantiomeric ratio of the product remains constant throughout the entire reaction and the formed enantioenriched product does not racemize upon exposure to the reaction conditions. See the Supporting Information for details.
-
-
-
-
46
-
-
84939567015
-
-
For corner/edge-coordinated cyclopropanes as intermediates in gold-catalyzed olefin cyclopropanation, see
-
For corner/edge-coordinated cyclopropanes as intermediates in gold-catalyzed olefin cyclopropanation, see
-
-
-
-
47
-
-
80052858561
-
-
for generic, metal-σ complexes of cyclopropane, see
-
V. Lõpez-Carrillo, N. Huguet, A. Mosquera, A. M. Echavarren, Chem. Eur. J. 2011, 17, 10972; for generic, metal-σ complexes of cyclopropane, see
-
(2011)
Chem. Eur. J.
, vol.17
, pp. 10972
-
-
Lõpez-Carrillo, V.1
Huguet, N.2
Mosquera, A.3
Echavarren, A.M.4
-
48
-
-
0011455075
-
-
A. Cutler, R. W. Fish, W. W. Giering, M. Rosenblum, J. Am. Chem. Soc. 1972, 94, 4354.
-
(1972)
J. Am. Chem. Soc.
, vol.94
, pp. 4354
-
-
Cutler, A.1
Fish, R.W.2
Giering, W.W.3
Rosenblum, M.4
-
49
-
-
84939573265
-
-
See NMR studies in the Supporting Information for details
-
See NMR studies in the Supporting Information for details.
-
-
-
-
50
-
-
84939576091
-
-
More-detailed studies are underway to elucidate the true origin of this unique phenomenon. For the preparation of mononuclear complex L17 AuCl, see the Supporting Information
-
More-detailed studies are underway to elucidate the true origin of this unique phenomenon. For the preparation of mononuclear complex L17 AuCl, see the Supporting Information.
-
-
-
-
51
-
-
38849130630
-
-
C. Lalli, A. Trabocchi, G. Menchi, A. Guarna, Synlett 2008, 189.
-
(2008)
Synlett
, pp. 189
-
-
Lalli, C.1
Trabocchi, A.2
Menchi, G.3
Guarna, A.4
-
52
-
-
34548792285
-
-
T. Ok, A. Jeon, J. Lee, J. H. Lim, C. S. Hong, H.-S. Lee, J. Org. Chem. 2007, 72, 7390
-
(2007)
J. Org. Chem.
, vol.72
, pp. 7390
-
-
Ok, T.1
Jeon, A.2
Lee, J.3
Lim, J.H.4
Hong, C.S.5
Lee, H.-S.6
-
53
-
-
79955453983
-
-
for a review on donor-acceptor cyclopropanes, see
-
A. G. Smith, M. C. Slade, J. S. Johnson, Org. Lett. 2011, 13, 1996; for a review on donor-acceptor cyclopropanes, see
-
(2011)
Org. Lett.
, vol.13
, pp. 1996
-
-
Smith, A.G.1
Slade, M.C.2
Johnson, J.S.3
-
54
-
-
84901449253
-
-
T. F. Schneider, J. Kasche, D. B. Werz, Angew. Chem. Int. Ed. 2014, 53, 5504
-
(2014)
Angew. Chem. Int. Ed.
, vol.53
, pp. 5504
-
-
Schneider, T.F.1
Kasche, J.2
Werz, D.B.3
-
55
-
-
84905366483
-
-
Angew. Chem. 2014, 126, 5608.
-
(2014)
Angew. Chem.
, vol.126
, pp. 5608
-
-
-
56
-
-
84939565107
-
-
Prior syntheses of 15
-
Prior syntheses of 15
-
-
-
-
57
-
-
79952161685
-
-
B. Mao, K. Geurts, M. Fananas-Mastrál, A. W. van Zijl, S. P. Fletcher, A. J. Minnaard, B. L. Feringa, Org. Lett. 2011, 13, 948
-
(2011)
Org. Lett.
, vol.13
, pp. 948
-
-
Mao, B.1
Geurts, K.2
Fananas-Mastrál, M.3
Van Zijl, A.W.4
Fletcher, S.P.5
Minnaard, A.J.6
Feringa, B.L.7
-
58
-
-
65449144684
-
-
A. Armstrong, C. Ashraff, H. Chung, L. Murtagh, Tetrahedron 2009, 65, 4490
-
(2009)
Tetrahedron
, vol.65
, pp. 4490
-
-
Armstrong, A.1
Ashraff, C.2
Chung, H.3
Murtagh, L.4
-
59
-
-
0035826638
-
-
C. Forzato, R. Gandolfi, F. Molinari, P. Nitti, G. Pitaccoa, E. Valentina, Tetrahedron: Asymmetry 2001, 12, 1039
-
(2001)
Tetrahedron: Asymmetry
, vol.12
, pp. 1039
-
-
Forzato, C.1
Gandolfi, R.2
Molinari, F.3
Nitti, P.4
Pitaccoa, G.5
Valentina, E.6
-
60
-
-
0001349316
-
-
C. W. Jefford, A. W. Sledeski, J. Boukouvalas, Helv. Chim. Acta 1989, 72, 1362
-
(1989)
Helv. Chim. Acta
, vol.72
, pp. 1362
-
-
Jefford, C.W.1
Sledeski, A.W.2
Boukouvalas, J.3
-
61
-
-
0030893869
-
-
S. Fukuzawa, K. Seki, M. Tatsuzawa, K. Mutoh, J. Am. Chem. Soc. 1997, 119, 1482
-
(1997)
J. Am. Chem. Soc.
, vol.119
, pp. 1482
-
-
Fukuzawa, S.1
Seki, K.2
Tatsuzawa, M.3
Mutoh, K.4
-
62
-
-
0029165982
-
-
H. Takahata, Y. Uchida, T. Momose, J. Org. Chem. 1995, 60, 5628
-
(1995)
J. Org. Chem.
, vol.60
, pp. 5628
-
-
Takahata, H.1
Uchida, Y.2
Momose, T.3
-
63
-
-
84859445240
-
-
D. A. Devalankar, P. V. Chouthaiwale, A. Sudalai, Tetrahedron: Asymmetry 2012, 23, 240.
-
(2012)
Tetrahedron: Asymmetry
, vol.23
, pp. 240
-
-
Devalankar, D.A.1
Chouthaiwale, P.V.2
Sudalai, A.3
|