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1
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0041878778
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For a general review, see: and references cited therein.
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For a general review, see:. Denmark S.E., and Fu J. Chem. Rev. 103 (2003) 2763 and references cited therein.
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Chem. Rev.
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Denmark, S.E.1
Fu, J.2
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2
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42149130246
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For recent examples on the asymmetric allylation of aldehydes, see:
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For recent examples on the asymmetric allylation of aldehydes, see:. Malkov A.V., Ramirez-Lopez P., Biedermannova L., Rulisek L., Dufkova L., Kotora M., Zhu F., and Kocovsky P. J. Am. Chem. Soc. 130 (2008) 5341
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J. Am. Chem. Soc.
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Malkov, A.V.1
Ramirez-Lopez, P.2
Biedermannova, L.3
Rulisek, L.4
Dufkova, L.5
Kotora, M.6
Zhu, F.7
Kocovsky, P.8
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4
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34247126420
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Liu L.-y., Sun J., Liu N., Chang W.-x., and Li J. Tetrahedron: Asymmetry 18 (2007) 710
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(2007)
Tetrahedron: Asymmetry
, vol.18
, pp. 710
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Liu, L.-y.1
Sun, J.2
Liu, N.3
Chang, W.-x.4
Li, J.5
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9
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33645007092
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Chen M., Zheng Y., Fan S., Gao G., Yang L., Tian L., Du Y., Tang F., and Hua W. Synth. Commun. 36 (2006) 1063
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(2006)
Synth. Commun.
, vol.36
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Chen, M.1
Zheng, Y.2
Fan, S.3
Gao, G.4
Yang, L.5
Tian, L.6
Du, Y.7
Tang, F.8
Hua, W.9
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10
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33750968173
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Chai Q., Song C., Sun Z., Ma Y., Ma C., Dai Y., and Andrus M.B. Tetrahedron Lett. 47 (2006) 8611
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(2006)
Tetrahedron Lett.
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, pp. 8611
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Chai, Q.1
Song, C.2
Sun, Z.3
Ma, Y.4
Ma, C.5
Dai, Y.6
Andrus, M.B.7
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13
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23644459055
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Chen M., Guo S., Zheng Y., Chen L., Tang F., and Hua W. Heterocycl. Commun. 11 (2005) 285
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(2005)
Heterocycl. Commun.
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Chen, M.1
Guo, S.2
Zheng, Y.3
Chen, L.4
Tang, F.5
Hua, W.6
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23
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0000544839
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Recently diastereoselective allylation was reported
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Tanaka K., Yoda H., Isobe Y., and Kaji A. J. Org. Chem. 51 (1986) 1856 Recently diastereoselective allylation was reported
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(1986)
J. Org. Chem.
, vol.51
, pp. 1856
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Tanaka, K.1
Yoda, H.2
Isobe, Y.3
Kaji, A.4
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24
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39649097618
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Nishigaichi Y., Tamura K., Ueda N., Iwamoto H., and Takuwa A. Tetrahedron Lett. 49 (2008) 2124
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(2008)
Tetrahedron Lett.
, vol.49
, pp. 2124
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Nishigaichi, Y.1
Tamura, K.2
Ueda, N.3
Iwamoto, H.4
Takuwa, A.5
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26
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18644380296
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Janecki T., Blaszczyk E., Studzian K., Janecka A., Krajewska U., and Rosalski M. J. Med. Chem. 48 (2005) 3516
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(2005)
J. Med. Chem.
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Janecki, T.1
Blaszczyk, E.2
Studzian, K.3
Janecka, A.4
Krajewska, U.5
Rosalski, M.6
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28
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45649083673
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For recent examples, see:
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For recent examples, see:. Isabelle C., Françoise Z., Jacques L., and Jean V. Tetrahedron 64 (2008) 2441
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(2008)
Tetrahedron
, vol.64
, pp. 2441
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Isabelle, C.1
Françoise, Z.2
Jacques, L.3
Jean, V.4
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30
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33750046044
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Le Lamer A.-C., Gouault N., David M., Boustie J., and Uriac P. J. Comb. Chem. 8 (2006) 643
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(2006)
J. Comb. Chem.
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, pp. 643
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Le Lamer, A.-C.1
Gouault, N.2
David, M.3
Boustie, J.4
Uriac, P.5
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35
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12344274699
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For recent examples, see:
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For recent examples, see:. Lu J., Ji S.-J., Teo Y.-C., and Loh T.-P. Org. Lett. 7 (2005) 159
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(2005)
Org. Lett.
, vol.7
, pp. 159
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Lu, J.1
Ji, S.-J.2
Teo, Y.-C.3
Loh, T.-P.4
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38
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25144446723
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Lu J., Hong M.-L., Ji S.-J., Teo Y.-C., and Loh T.-P. Chem. Commun. (2005) 4217
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(2005)
Chem. Commun.
, pp. 4217
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Lu, J.1
Hong, M.-L.2
Ji, S.-J.3
Teo, Y.-C.4
Loh, T.-P.5
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41
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45649083354
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note
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A general method for preparation of β-amido allylstannanes was reported in Ref. 2b.
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42
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45649083010
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note
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2+Na: 290.1157, found 290.1128.
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43
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0342547018
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The absolute configuration of the stereogenic center of 6a was easily determined to be S after derivation to the corresponding α-methylene-γ-butyrolactone 7a as shown below, see: {A figure is presented}
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The absolute configuration of the stereogenic center of 6a was easily determined to be S after derivation to the corresponding α-methylene-γ-butyrolactone 7a as shown below, see:. Csuk R., Schröder C., Hutter S., and Mohr K. Tetrahedron: Asymmetry 8 (1997) 1411 {A figure is presented}
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(1997)
Tetrahedron: Asymmetry
, vol.8
, pp. 1411
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Csuk, R.1
Schröder, C.2
Hutter, S.3
Mohr, K.4
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44
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45549122277
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note
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2a after cyclization again to the corresponding lactone 7b as shown below.{A figure is presented}
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