Zobrazeno 1 - 10
of 15
pro vyhledávání: '"O. A. Dasse"'
Autor:
O. A. Dasse, R.K. Kondru, C.E. Schwartz, D. Zou, A. Volosov, H.-X. Zhai, P. Collart, K. Hamilton, J. B. Eckman, J.-M. Nicolas, J. L. Evans, E. Hill, P. J. Higgins, F. Chan, Jeremy Kintigh
Publikováno v:
Letters in Drug Design & Discovery. 4:263-271
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::3fd1c21b41b2fd9cbe7dfd15c8f0bf1e
https://doi.org/10.2174/157018007784619989
https://doi.org/10.2174/157018007784619989
Publikováno v:
The Journal of Organic Chemistry. 64:2475-2485
The A/B and the C/D/E rings of the xestobergsterol skeleton have been stereoselectively synthesized starting with testosterone and epiandrosterone, respectively. A deconjugative ketalization of the A-ring enone of testosterone provided a handle for f
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::4b577e4b7896a3915163847d715c4f05
https://doi.org/10.1021/jo982319w
https://doi.org/10.1021/jo982319w
Publikováno v:
Tetrahedron. 54:7033-7044
An approach to the synthesis of the histamine release inhibitor xestobergsterol is described. The intramolecular Pauson-Khand reaction was used to generate the D and E rings of the steroid.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::1ca352b379038ee55c27162e9fa7f628
https://doi.org/10.1016/s0040-4020(98)00345-7
https://doi.org/10.1016/s0040-4020(98)00345-7
Publikováno v:
Pure and Applied Chemistry. 70:1083-1090
Highly regioselective additions to allylic acetates, catalyzed by palladium (0), can be achieved by incorporation of a thioether or tertiary amine on the substrate. Reactions with malonate anion are highly selective for the terminus of the allyl moie
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::9e357c832cce47b9f875f7bae9c85ecc
https://doi.org/10.1351/pac199870051083
https://doi.org/10.1351/pac199870051083
Publikováno v:
The Journal of Organic Chemistry. 60:5093-5101
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::a1a44019a4f172221452b2d278b7cf77
https://doi.org/10.1021/jo00121a029
https://doi.org/10.1021/jo00121a029
Publikováno v:
ChemInform. 25
The Ireland ester enolate Claisen rearrangement gives rise to Z-trisubstituted alkenes via heteroatom mediated substrate pre-organization prior to rearrangement.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::1070dd2e1cb784e00e57bb2f6062da03
https://doi.org/10.1002/chin.199415076
https://doi.org/10.1002/chin.199415076
Publikováno v:
ChemInform. 26
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::2cbd8915538a200b5bf9a15c5cf71949
https://doi.org/10.1002/chin.199550031
https://doi.org/10.1002/chin.199550031
Autor:
M. K. Mollman, Marie E. Krafft, O. A. Dasse, A. M. Wilson, B. Shao, Y. Y. Cheung, Llorente V. R. Bonaga, Z. Fu
Publikováno v:
ChemInform. 27
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::ac35a09f2a12495dd4b2403e45c081b8
https://doi.org/10.1002/chin.199640044
https://doi.org/10.1002/chin.199640044
Publikováno v:
ChemInform. 29
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::e1b92bb326ac4644150e9af7956f1d54
https://doi.org/10.1002/chin.199830071
https://doi.org/10.1002/chin.199830071
Publikováno v:
ChemInform. 29
An approach to the synthesis of the histamine release inhibitor xestobergsterol is described. The intramolecular Pauson-Khand reaction was used to generate the D and E rings of the steroid.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::4a06e16ad7f503cb69d5245620d745fa
https://doi.org/10.1002/chin.199841192
https://doi.org/10.1002/chin.199841192