3 pages, 1 scheme.-- Part 29 in the series “New Sources of Steroid Sapogenins”. For Part 28 see González, A. G., Francisco, C. G., Freire, R., Hernández, R., Salazar, J. A. and Suárez, E. (1975) Phytochemistry 14, 2259, http://digital.csic.es/handle/10261/15180The structure of andesgenin, a new steroid sapogenin isolated from Solanum hypomalacophyllum, was determined on the basis of spectral data and synthesis of its Huang-Minlon reduction products to be (20S, 22R, 25R)-3β-hydroxy-5α-cholestan-22,26-epoxy-4,23-dione.One of us (R.H.) thanks the CSIC for a postdoctoral fellowship
Fig. 3. Key NOESY correlations of compounds 1, 2, 4 and 7.Published as part of Xu, Zhen-Peng, Liu, Y...
International audienceSteroidal alkaloids are secondary metabolites mainly isolated from species of ...
Fig. 1. Chemical structures of compounds 1 to 13.Published as part of Liu, Liang-Yu, Yang, Yu-Ke, Wa...
4 pages, 1 table, 2 schemes.-- Part XVIII: A. G. González, R. Freire, R. Hernández, J. A. Salazar an...
2 pages, 1 scheme.-- Part 27 in the series New Sources of Steroid Sapogenins. For Part 26 see Gonzál...
4 pages, 2 schemes.-- Part 28 in the series “New Sources of Steroid Sapogenins”. For Part 27 see Gon...
7 pages, 1 table, 1 scheme.-- For Part XVII see A.G. González, R. Freire Barreira, C. García Francis...
Fig. 2. 1H–1H COSY of the aglycones and key HMBC correlations of compounds 1–8.Published as part of ...
Fig. 1. Chemical structures of compounds 1–6.Published as part of Kaunda, Joseph Sakah, Qin, Xu-Jie,...
Fig. 1. Chemical structures of compounds 1–8.Published as part of Xu, Zhen-Peng, Liu, Yan, Wang, Si-...
4 pages, 1 scheme.-- Part XXXI in the series “New Sources of Steroid Sapogenins”. For Part XXX, see ...
Fig. 2. Key 1H–1H COSY and HMBC correlations of 1 and 6.Published as part of Kaunda, Joseph Sakah, Q...
Fig. 4. Plausible biosynthesis pathway of 16,26-epoxy-furostanol saponins.Published as part of Xu, Z...
Fig. 4. Key 1H–1H COSY, HMBC, ROESY correlations of 4.Published as part of Kaunda, Joseph Sakah, Qin...
Fig. 3. Key ROESY correlations for the aglycone moiety of 1.Published as part of Kaunda, Joseph Saka...
Fig. 3. Key NOESY correlations of compounds 1, 2, 4 and 7.Published as part of Xu, Zhen-Peng, Liu, Y...
International audienceSteroidal alkaloids are secondary metabolites mainly isolated from species of ...
Fig. 1. Chemical structures of compounds 1 to 13.Published as part of Liu, Liang-Yu, Yang, Yu-Ke, Wa...
4 pages, 1 table, 2 schemes.-- Part XVIII: A. G. González, R. Freire, R. Hernández, J. A. Salazar an...
2 pages, 1 scheme.-- Part 27 in the series New Sources of Steroid Sapogenins. For Part 26 see Gonzál...
4 pages, 2 schemes.-- Part 28 in the series “New Sources of Steroid Sapogenins”. For Part 27 see Gon...
7 pages, 1 table, 1 scheme.-- For Part XVII see A.G. González, R. Freire Barreira, C. García Francis...
Fig. 2. 1H–1H COSY of the aglycones and key HMBC correlations of compounds 1–8.Published as part of ...
Fig. 1. Chemical structures of compounds 1–6.Published as part of Kaunda, Joseph Sakah, Qin, Xu-Jie,...
Fig. 1. Chemical structures of compounds 1–8.Published as part of Xu, Zhen-Peng, Liu, Yan, Wang, Si-...
4 pages, 1 scheme.-- Part XXXI in the series “New Sources of Steroid Sapogenins”. For Part XXX, see ...
Fig. 2. Key 1H–1H COSY and HMBC correlations of 1 and 6.Published as part of Kaunda, Joseph Sakah, Q...
Fig. 4. Plausible biosynthesis pathway of 16,26-epoxy-furostanol saponins.Published as part of Xu, Z...
Fig. 4. Key 1H–1H COSY, HMBC, ROESY correlations of 4.Published as part of Kaunda, Joseph Sakah, Qin...
Fig. 3. Key ROESY correlations for the aglycone moiety of 1.Published as part of Kaunda, Joseph Saka...
Fig. 3. Key NOESY correlations of compounds 1, 2, 4 and 7.Published as part of Xu, Zhen-Peng, Liu, Y...
International audienceSteroidal alkaloids are secondary metabolites mainly isolated from species of ...
Fig. 1. Chemical structures of compounds 1 to 13.Published as part of Liu, Liang-Yu, Yang, Yu-Ke, Wa...