Zobrazeno 1 - 10
of 13
pro vyhledávání: '"David A. Oare"'
Autor:
David A. Oare, I-hung Shih, Laura S. Lehman, Erik De Clercq, Eric Mabery, Steven S. Bondy, Weidong Zhong, Inge Vliegen, Matthew Paulson, Johan Neyts, Gerhard Pürstinger, Hans Reiser, Jan Paeshuyse, Nina Boddeker, Tine De Burghgraeve, William A. Lee
Publikováno v:
Journal of Hepatology
Background/Aims Following lead optimization, a set of substituted imidazopyridines was identified as potent and selective inhibitors of in vitro HCV replication. The particular characteristics of one of the most potent compounds in this series (5-[[3
ChemInform Abstract: Acyclic Stereocontrol in Michael Addition Reactions of Enamines and Enol Ethers
Autor:
David A. Oare, Clayton H. Heathcock
Publikováno v:
ChemInform. 22
Publikováno v:
The Journal of Organic Chemistry. 55:132-157
Autor:
David A. Oare, Clayton H. Heathcock
Publikováno v:
The Journal of Organic Chemistry. 55:157-172
Autor:
David A. Oare, Clayton H. Heathcock
Publikováno v:
Topics in Stereochemistry
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::a7186b6b57fde37d167b596a597f33fb
https://doi.org/10.1002/9780470147283.ch5
https://doi.org/10.1002/9780470147283.ch5
Autor:
Clayton H. Heathcock, David A. Oare
Publikováno v:
Topics in Stereochemistry, Volume 20
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::1ed614d1b5d915b79d301f9562dec8f6
https://doi.org/10.1002/9780470147290.ch2
https://doi.org/10.1002/9780470147290.ch2
Autor:
David A. Oare, Clayton H. Heathcock
Publikováno v:
ChemInform. 21
Publikováno v:
ChemInform. 21
Autor:
Bruno Canard, Barbara Selisko, Weidong Zhong, David A. Oare, Steven S. Bondy, Hélène Dutartre, Johan Neyts, Inge Vliegen, Laura S. Lehman, Sofie Roofthooft, Nina Boddeker, William A. Lee, Jan Paeshuyse, Gerhard Pürstinger, Erik De Clercq
Publikováno v:
Antiviral Research. 74:A37-A37
Autor:
Clayton H. Heathcock, David A. Oare
Publikováno v:
Tetrahedron Letters. 27:6169-6172
Preformed lithium enolates of ketones react with acyclic α,β-unsaturated ketones to give 1,5-diketones in good chemical yields. A strong correlation exists between enolate geometry and product stereochemistry; enolates having the Z configuration pr