-
3
-
-
70350494926
-
-
R. Giri, B.-F. Shi, K. M. Engle, N. Maugel, J.-Q. Yu, Chem. Soc. Rev. 2009, 38, 3242–3272.
-
(2009)
Chem. Soc. Rev.
, vol.38
, pp. 3242-3272
-
-
Giri, R.1
Shi, B.-F.2
Engle, K.M.3
Maugel, N.4
Yu, J.-Q.5
-
4
-
-
77349105953
-
-
M. P. Doyle, R. Duffy, M. Ratnikov, L. Zhou, Chem. Rev. 2010, 110, 704–724.
-
(2010)
Chem. Rev.
, vol.110
, pp. 704-724
-
-
Doyle, M.P.1
Duffy, R.2
Ratnikov, M.3
Zhou, L.4
-
6
-
-
84872864159
-
-
Y. Kuninobu, K. Yamauchi, N. Tamura, T. Seiki, K. Takai, Angew. Chem. Int. Ed. 2013, 52, 1520–1522;
-
(2013)
Angew. Chem. Int. Ed.
, vol.52
, pp. 1520-1522
-
-
Kuninobu, Y.1
Yamauchi, K.2
Tamura, N.3
Seiki, T.4
Takai, K.5
-
7
-
-
84885651749
-
-
Angew. Chem. 2013, 125, 1560–1562.
-
(2013)
Angew. Chem.
, vol.125
, pp. 1560-1562
-
-
-
8
-
-
84960533133
-
-
M. Murai, Y. Takeuchi, K. Yamauchi, Y. Kuninobu, K. Takai, Chem. Eur. J. 2016, 22, 6048–6058.
-
(2016)
Chem. Eur. J.
, vol.22
, pp. 6048-6058
-
-
Murai, M.1
Takeuchi, Y.2
Yamauchi, K.3
Kuninobu, Y.4
Takai, K.5
-
9
-
-
84928801929
-
-
T. Shibata, T. Shizuno, T. Sasaki, Chem. Commun. 2015, 51, 7802–7804.
-
(2015)
Chem. Commun.
, vol.51
, pp. 7802-7804
-
-
Shibata, T.1
Shizuno, T.2
Sasaki, T.3
-
10
-
-
84930507701
-
-
Q. W. Zhang, K. An, L. C. Liu, Y. Yue, W. He, Angew. Chem. Int. Ed. 2015, 54, 6918–6921;
-
(2015)
Angew. Chem. Int. Ed.
, vol.54
, pp. 6918-6921
-
-
Zhang, Q.W.1
An, K.2
Liu, L.C.3
Yue, Y.4
He, W.5
-
11
-
-
84939531633
-
-
Angew. Chem. 2015, 127, 7022–7025.
-
(2015)
Angew. Chem.
, vol.127
, pp. 7022-7025
-
-
-
12
-
-
84934908417
-
-
M. Murai, K. Matsumoto, Y. Takeuchi, K. Takai, Org. Lett. 2015, 17, 3102–3105.
-
(2015)
Org. Lett.
, vol.17
, pp. 3102-3105
-
-
Murai, M.1
Matsumoto, K.2
Takeuchi, Y.3
Takai, K.4
-
13
-
-
84930664672
-
-
T. Lee, T. W. Wilson, R. Berg, P. Ryberg, J. F. Hartwig, J. Am. Chem. Soc. 2015, 137, 6742–6745.
-
(2015)
J. Am. Chem. Soc.
, vol.137
, pp. 6742-6745
-
-
Lee, T.1
Wilson, T.W.2
Berg, R.3
Ryberg, P.4
Hartwig, J.F.5
-
14
-
-
84930631159
-
-
M. Murai, H. Takeshima, H. Morita, Y. Kuninobu, K. Takai, J. Org. Chem. 2015, 80, 5407–5414.
-
(2015)
J. Org. Chem.
, vol.80
, pp. 5407-5414
-
-
Murai, M.1
Takeshima, H.2
Morita, H.3
Kuninobu, Y.4
Takai, K.5
-
16
-
-
83055161417
-
-
M. Wasa, K. M. Engle, D. W. Lin, E. J. Yoo, J.-Q. Yu, J. Am. Chem. Soc. 2011, 133, 19598–19601.
-
(2011)
J. Am. Chem. Soc.
, vol.133
, pp. 19598-19601
-
-
Wasa, M.1
Engle, K.M.2
Lin, D.W.3
Yoo, E.J.4
Yu, J.-Q.5
-
17
-
-
84922767264
-
-
K. S. L. Chan, H.-Y. Fu, J.-Q. Yu, J. Am. Chem. Soc. 2015, 137, 2042–2046.
-
(2015)
J. Am. Chem. Soc.
, vol.137
, pp. 2042-2046
-
-
Chan, K.S.L.1
Fu, H.-Y.2
Yu, J.-Q.3
-
19
-
-
84875781890
-
-
Angew. Chem. 2012, 124, 13014–13017.
-
(2012)
Angew. Chem.
, vol.124
, pp. 13014-13017
-
-
-
20
-
-
84938925256
-
-
J. Pedroni, T. Saget, P. A. Donets, N. Cramer, Chem. Sci. 2015, 6, 5164–5171.
-
(2015)
Chem. Sci.
, vol.6
, pp. 5164-5171
-
-
Pedroni, J.1
Saget, T.2
Donets, P.A.3
Cramer, N.4
-
22
-
-
84977760760
-
-
Angew. Chem. 2015, 127, 11992–11995.
-
(2015)
Angew. Chem.
, vol.127
, pp. 11992-11995
-
-
-
23
-
-
55349127837
-
-
Formation of carbon–heteroatom bonds by enantioselective deprotonation of cyclopropyl C−H bonds with a stoichiometric amount of sparteine has been reported
-
Formation of carbon–heteroatom bonds by enantioselective deprotonation of cyclopropyl C−H bonds with a stoichiometric amount of sparteine has been reported: S. Lauru, N. S. Simpkins, D. Gethin, C. Wilson, Chem. Commun. 2008, 5390–5392.
-
(2008)
Chem. Commun.
, pp. 5390-5392
-
-
Lauru, S.1
Simpkins, N.S.2
Gethin, D.3
Wilson, C.4
-
24
-
-
84892970497
-
-
N. Ghavtadze, F. S. Melkonyan, A. V. Gulevich, C. Huang, V. Gevorgyan, Nat. Chem. 2014, 6, 122–125.
-
(2014)
Nat. Chem.
, vol.6
, pp. 122-125
-
-
Ghavtadze, N.1
Melkonyan, F.S.2
Gulevich, A.V.3
Huang, C.4
Gevorgyan, V.5
-
25
-
-
84938841741
-
-
C. Chen, M. Guan, J. Zhang, Z. Wen, Y. Zhao, Org. Lett. 2015, 17, 3646–3649.
-
(2015)
Org. Lett.
, vol.17
, pp. 3646-3649
-
-
Chen, C.1
Guan, M.2
Zhang, J.3
Wen, Z.4
Zhao, Y.5
-
26
-
-
84872537508
-
-
Y. Kuninobu, T. Nakahara, H. Takeshima, K. Takai, Org. Lett. 2013, 15, 426–428.
-
(2013)
Org. Lett.
, vol.15
, pp. 426-428
-
-
Kuninobu, Y.1
Nakahara, T.2
Takeshima, H.3
Takai, K.4
-
27
-
-
84888369128
-
-
T. Mita, K. Michigami, Y. Sato, Chem. Asian J. 2013, 8, 2970–2973.
-
(2013)
Chem. Asian J.
, vol.8
, pp. 2970-2973
-
-
Mita, T.1
Michigami, K.2
Sato, Y.3
-
28
-
-
84900328445
-
-
B. Li, M. Driess, J. F. Hartwig, J. Am. Chem. Soc. 2014, 136, 6586–6589.
-
(2014)
J. Am. Chem. Soc.
, vol.136
, pp. 6586-6589
-
-
Li, B.1
Driess, M.2
Hartwig, J.F.3
-
29
-
-
0037997232
-
-
A diastereoselective reduction of cyclopropanone has been reported
-
A diastereoselective reduction of cyclopropanone has been reported: G. S. Zaitseva, I. F. Lutsenko, A. V. Kisin, Y. I. Baukov, J. Lorberth, J. Organomet. Chem. 1988, 345, 253–262.
-
(1988)
J. Organomet. Chem.
, vol.345
, pp. 253-262
-
-
Zaitseva, G.S.1
Lutsenko, I.F.2
Kisin, A.V.3
Baukov, Y.I.4
Lorberth, J.5
-
32
-
-
84905368533
-
-
Q. Li, M. Driess, J. F. Hartwig, Angew. Chem. Int. Ed. 2014, 53, 8471–8474;
-
(2014)
Angew. Chem. Int. Ed.
, vol.53
, pp. 8471-8474
-
-
Li, Q.1
Driess, M.2
Hartwig, J.F.3
-
33
-
-
84919380516
-
-
Angew. Chem. 2014, 126, 8611–8614.
-
(2014)
Angew. Chem.
, vol.126
, pp. 8611-8614
-
-
-
36
-
-
0028802899
-
-
A. G. Bessmertnykh, K. A. Blinov, Y. K. Grishin, N. A. Donskaya, I. P. Beletskaya, Tetrahedron Lett. 1995, 36, 7901–7904.
-
(1995)
Tetrahedron Lett.
, vol.36
, pp. 7901-7904
-
-
Bessmertnykh, A.G.1
Blinov, K.A.2
Grishin, Y.K.3
Donskaya, N.A.4
Beletskaya, I.P.5
-
37
-
-
0030850587
-
-
A. G. Bessmertnykh, K. A. Blinov, Y. K. Grishin, N. A. Donskaya, E. V. Tveritinova, N. M. Yur eva, I. P. Beletskaya, J. Org. Chem. 1997, 62, 6069–6076.
-
(1997)
J. Org. Chem.
, vol.62
, pp. 6069-6076
-
-
Bessmertnykh, A.G.1
Blinov, K.A.2
Grishin, Y.K.3
Donskaya, N.A.4
Tveritinova, E.V.5
Yur eva, N.M.6
Beletskaya, I.P.7
-
38
-
-
85043096943
-
-
entries 6, 7, 9).
-
Ring opening of the cyclopropane by the hydrosilyl group was observed under the conditions listed in Table 1 (entries 6, 7, 9).
-
-
-
-
39
-
-
85043134678
-
-
The sensitivity of oxasilolanes to silica and the similar polarity or boiling points of oxasilolanes to side products or ligands caused the yields of pure, isolated material to be lower than those determined by GC or NMR analysis.
-
The sensitivity of oxasilolanes to silica and the similar polarity or boiling points of oxasilolanes to side products or ligands caused the yields of pure, isolated material to be lower than those determined by GC or NMR analysis.
-
-
-
-
41
-
-
84933531292
-
-
Angew. Chem. 2001, 113, 40–75.
-
(2001)
Angew. Chem.
, vol.113
, pp. 40-75
-
-
-
43
-
-
0001015795
-
-
Angew. Chem. 1998, 110, 2092–2118.
-
(1998)
Angew. Chem.
, vol.110
, pp. 2092-2118
-
-
-
45
-
-
84863668849
-
-
Angew. Chem. 2012, 124, 3120–3126.
-
(2012)
Angew. Chem.
, vol.124
, pp. 3120-3126
-
-
-
47
-
-
54749136535
-
-
H. Ito, Y. Kosaka, K. Nonoyama, Y. Sasaki, M. Sawamura, Angew. Chem. Int. Ed. 2008, 47, 7424–7427;
-
(2008)
Angew. Chem. Int. Ed.
, vol.47
, pp. 7424-7427
-
-
Ito, H.1
Kosaka, Y.2
Nonoyama, K.3
Sasaki, Y.4
Sawamura, M.5
-
48
-
-
74549156927
-
-
Angew. Chem. 2008, 120, 7534–7537.
-
(2008)
Angew. Chem.
, vol.120
, pp. 7534-7537
-
-
|