-
1
-
-
0035813890
-
-
Representative examples of natural products:
-
Representative examples of natural products:. Paterson I., Chen D.Y.-K., Coster M.J., Acena J.L., Bach J., Gibson K.R., Keown L.E., Oballa R.M., Trieselmann T., Wallace D.J., Hodgson A.P., and Norcross R.D. Angew. Chem., Int. Ed. 40 (2001) 4055-4060
-
(2001)
Angew. Chem., Int. Ed.
, vol.40
, pp. 4055-4060
-
-
Paterson, I.1
Chen, D.Y.-K.2
Coster, M.J.3
Acena, J.L.4
Bach, J.5
Gibson, K.R.6
Keown, L.E.7
Oballa, R.M.8
Trieselmann, T.9
Wallace, D.J.10
Hodgson, A.P.11
Norcross, R.D.12
-
4
-
-
0141664612
-
-
Barton D.H.R., Nakanishi K., and Meth-Cohn O. (Eds), Pergamon, Oxford, UK
-
Misra M., Luthra R., Singh K.L., and Sushil K. In: Barton D.H.R., Nakanishi K., and Meth-Cohn O. (Eds). Comprehensive Natural Products Chemistry Vol. 4 (1999), Pergamon, Oxford, UK 25
-
(1999)
Comprehensive Natural Products Chemistry
, vol.4
, pp. 25
-
-
Misra, M.1
Luthra, R.2
Singh, K.L.3
Sushil, K.4
-
5
-
-
0000214961
-
-
Representative examples in organic synthesis:
-
Representative examples in organic synthesis:. Noyori R., and Kato M. Bull. Chem. Soc. Jpn. 47 (1974) 1460-1466
-
(1974)
Bull. Chem. Soc. Jpn.
, vol.47
, pp. 1460-1466
-
-
Noyori, R.1
Kato, M.2
-
21
-
-
0038603070
-
-
van Lingen H.L., Zhuang W., Hansen T., Rutjes F.P.J.T., and Jørgensen K.A. Org. Biomol. Chem. 1 (2003) 1953-1958
-
(2003)
Org. Biomol. Chem.
, vol.1
, pp. 1953-1958
-
-
van Lingen, H.L.1
Zhuang, W.2
Hansen, T.3
Rutjes, F.P.J.T.4
Jørgensen, K.A.5
-
31
-
-
33646142092
-
-
For papers see:
-
For papers see:. Mase N., Watanabe K., Yoda H., Takabe K., Tanaka F., and Barbas III C.F. J. Am. Chem. Soc. 128 (2006) 4966-4967
-
(2006)
J. Am. Chem. Soc.
, vol.128
, pp. 4966-4967
-
-
Mase, N.1
Watanabe, K.2
Yoda, H.3
Takabe, K.4
Tanaka, F.5
Barbas III, C.F.6
-
32
-
-
31444456557
-
-
Mase N., Nakai Y., Ohara N., Yoda H., Takabe K., Tanaka F., and Barbas III C.F. J. Am. Chem. Soc. 128 (2006) 734-735
-
(2006)
J. Am. Chem. Soc.
, vol.128
, pp. 734-735
-
-
Mase, N.1
Nakai, Y.2
Ohara, N.3
Yoda, H.4
Takabe, K.5
Tanaka, F.6
Barbas III, C.F.7
-
39
-
-
18144384748
-
-
The enantiomeric excess (ee) of tandem product 11 (synthesized from chiral diamine 2e-catalysis) was 11% and was determined by chiral-phase HPLC analyses. The absolute stereochemistry was not determined. For syntheses of Basavaiah-Baylis-Hillman product 11 by other methods, see:
-
The enantiomeric excess (ee) of tandem product 11 (synthesized from chiral diamine 2e-catalysis) was 11% and was determined by chiral-phase HPLC analyses. The absolute stereochemistry was not determined. For syntheses of Basavaiah-Baylis-Hillman product 11 by other methods, see:. Reingold I.D., Butterfield A.M., Daglen B.C., Walters Jr. R.S., Allen K., Scheuring S., Kratz K., Gembicky M., and Baran P. Tetrahedron Lett. 46 (2005) 3835-3837
-
(2005)
Tetrahedron Lett.
, vol.46
, pp. 3835-3837
-
-
Reingold, I.D.1
Butterfield, A.M.2
Daglen, B.C.3
Walters Jr., R.S.4
Allen, K.5
Scheuring, S.6
Kratz, K.7
Gembicky, M.8
Baran, P.9
-
47
-
-
33748982708
-
-
Kaufman, H. A.; Napier, R. P. Ger. Offen., 1970, pp 7. CODEN: GWXXBX DE 2016666 19701105; Chem. Abstr. 1970, 74:30977 (Patent written in German).
-
-
-
|