-
1
-
-
0003445429
-
-
E. N. Jacobsen, A. Pfaltz and H. Yamamoto, Springer-Verlag, Berlin
-
Comprehensive Asymmetric Catalysis II, ed., E. N. Jacobsen, A. Pfaltz, and, H. Yamamoto Springer-Verlag, Berlin, 1999
-
(1999)
Comprehensive Asymmetric Catalysis II, Ed.
-
-
-
3
-
-
28644442668
-
-
E. N. Jacobsen, A. Pfaltz and H. Yamamoto, Springer-Verlag, Berlin
-
Comprehensive Asymmetric Catalysis: Supplement 1, ed., E. N. Jacobsen, A. Pfaltz, and, H. Yamamoto Springer-Verlag, Berlin, 2003
-
(2003)
Comprehensive Asymmetric Catalysis: Supplement 1, Ed.
-
-
-
4
-
-
20444390269
-
-
S. V. Malhotra, American Chemical Society, Washington, DC
-
Methodologies in Asymmetric Catalysis, ed., S. V. Malhotra American Chemical Society, Washington, DC, 2004
-
(2004)
Methodologies in Asymmetric Catalysis, Ed.
-
-
-
10
-
-
0035356736
-
-
Y. Yamamoto R. Hattori T. Miwa Y. Nakagai T. Kubota C. Yamamoto Y. Okamoto K. Itoh J. Org. Chem. 2001 66 3865
-
(2001)
J. Org. Chem.
, vol.66
, pp. 3865
-
-
Yamamoto, Y.1
Hattori, R.2
Miwa, T.3
Nakagai, Y.4
Kubota, T.5
Yamamoto, C.6
Okamoto, Y.7
Itoh, K.8
-
11
-
-
35349014208
-
-
D. -Y. Wang X. -P. Hu J. -D. Huang J. Deng S. -B. Yu Z. -C. Duan X. -F. Xu Z. Zheng Angew. Chem., Int. Ed. 2007 46 7810
-
(2007)
Angew. Chem., Int. Ed.
, vol.46
, pp. 7810
-
-
Wang, D.-Y.1
Hu, X.-P.2
Huang, J.-D.3
Deng, J.4
Yu S.-B5
Duan, Z.-C.6
Xu, X.-F.7
Zheng, Z.8
-
15
-
-
33646677236
-
-
L. Qiu F. Y. Kwong J. Wu W. H. Lam S. Chan W. -Y. Yu Y. -M. Li R. Guo Z. Zhou A. S. C. Chan J. Am. Chem. Soc. 2006 128 5955
-
(2006)
J. Am. Chem. Soc.
, vol.128
, pp. 5955
-
-
Qiu, L.1
Kwong, F.Y.2
Wu, J.3
Lam, W.H.4
Chan, S.5
Yu, W.-Y.6
Li, Y.-M.7
Guo, R.8
Zhou, Z.9
Chan, A.S.C.10
-
19
-
-
0345529029
-
-
A. V. Malkov M. Bell M. Orsini D. Pernazza A. Massa P. Herrmann P. Meghani P. Kocovsky J. Org. Chem. 2003 68 9659
-
(2003)
J. Org. Chem.
, vol.68
, pp. 9659
-
-
Malkov, A.V.1
Bell, M.2
Orsini, M.3
Pernazza, D.4
Massa, A.5
Herrmann, P.6
Meghani, P.7
Kocovsky, P.8
-
51
-
-
4544286694
-
-
A. Gutnov B. Heller C. Fischer H. -J. Drexler A. Spannenberg B. Sundermann C. Sundermann Angew. Chem., Int. Ed. 2004 43 3795
-
(2004)
Angew. Chem., Int. Ed.
, vol.43
, pp. 3795
-
-
Gutnov, A.1
Heller, B.2
Fischer, C.3
Drexler, H.-J.4
Spannenberg, A.5
Sundermann, B.6
Sundermann, C.7
-
53
-
-
11144315960
-
-
When adduct 3ac was heat at 80 °C in DCE for 1 h, a significant decrease of diastereomeric ratio was observed (from 10: 1 to 5: 1) As a reference experiment, the cycloaddition of alkynes 2a and 2c with a diyne, in place of enynes, was examined under the same reaction conditions: the reaction of alkyne 2c achieved much higher enantioselectivity than that of 2a (details in supplemental information). These results suggest that diastereoselectivity was determined by the induction of axial chirality at the stage of alkyne insertion
-
K. Tanaka G. Nishida A. Wada K. Noguchi Angew. Chem., Int. Ed. 2004 43 6510
-
(2004)
Angew. Chem., Int. Ed.
, vol.43
, pp. 6510
-
-
Tanaka, K.1
Nishida, G.2
Wada, A.3
Noguchi, K.4
|