Zobrazeno 1 - 10
of 36
pro vyhledávání: '"A J, Luzzio"'
Autor:
Xiaoming Zhang, William G. Dauben, Michael J. Luzzio, Shung C. Wu, Bipin Pandy, Robert T. Hendricks
Publikováno v:
Tetrahedron Letters. 36:2385-2388
Two efficient enantioselective syntheses of an A-ring precursor to 1 α,25-dihydroxyvitamin D3 have been developed. The key step in these sequences involves the stereoselective cyclopropanation of a chiral γ-alkoxy-α-diazo-β-keto ester. In one seq
Publikováno v:
ChemInform. 23
Publikováno v:
The Journal of Organic Chemistry. 55:918-924
La synthese du compose du titre necessite la preparation de l'intermediaire cle suivant: 3-hydroxymethyl-6-oxo-perhydropyrano [3,4-c] pyrrole-2-carboxylate de methyl; a partir du N-methoxycarbonyl glycinate de methyl et du 4-t-butoxycrotonate d'ethyl
Publikováno v:
Tetrahedron Letters. 31:6969-6972
A series of unsaturated α-diazo carbonyl compounds underwent enantioselective intramolecular cyclopropanation (ee = 4–77%) when treated with an enantiomerically pure chiral copper catalyst. The nature of the diazo substrate was critical: α-diazo
Autor:
D L, Emerson, R, Bendele, E, Brown, S, Chiang, J P, Desjardins, L C, Dihel, S C, Gill, M, Hamilton, J D, LeRay, L, Moon-McDermott, K, Moynihan, F C, Richardson, B, Tomkinson, M J, Luzzio, D, Baccanari
Publikováno v:
Clinical cancer research : an official journal of the American Association for Cancer Research. 6(7)
Lurtotecan is a clinically active water-soluble camptothecin analogue that has been formulated into a low-clearance unilamellar liposome, NX 211. Comparative studies between free drug and NX 211 have been performed assessing pharmacokinetics in nude
Autor:
Micheal J. Luzzio, E. Hinnant, J. Yates, Tiechao Li, Wuyi Wang, Robert Milburn, Giorgio Attardo, Stuart A. Noble
Publikováno v:
Bioorganicmedicinal chemistry letters. 8(13)
Novel antitumor 5,10-dihydro-5,10-dioxo-1 H -benzo[ g ]isochromene-3-carboxamides were discovered.
Autor:
Tona M. Gilmer, Michael J. Luzzio
Publikováno v:
Drug Discovery Today: Therapeutic Strategies. 2:297-298
Autor:
D L, Emerson, J M, Besterman, H R, Brown, M G, Evans, P P, Leitner, M J, Luzzio, J E, Shaffer, D D, Sternbach, D, Uehling, A, Vuong
Publikováno v:
Cancer research. 55(3)
The development of camptothecin-like compounds as inhibitors of topoisomerase I for the treatment of resistant tumors has generated clinical excitement in this new class of drugs. We have developed two novel water-soluble camptothecin analogues which
Autor:
Stephen T. Davis, Bill G. Benson, H. Neal Bramson, Dennis E. Chapman, Scott H. Dickerson, Karen M. Dold, Derek J. Eberwein, Mark Edelstein, Stephen V. Frye, Robert T. Gampe, Robert J. Griffin, Philip A. Harris, Anne M. Hassell, William D. Holmes, Robert N. Hunter, Victoria B. Knick, Karen Lackey, Brett Lovejoy, Michael J. Luzzio, Doris Murray, Patricia Parker, Warren J. Rocque, Lisa Shewchuk-Chapman, James M. Veal, Duncan H. Walker, Lee F. Kuyper
Publikováno v:
Science. 298:2327-2327