Уважаемые коллеги!
Буду признателен за следующие статьи:
1. T. W. Lee, J. R. Proudfoot, D. S. Thomson A concise asymmetric route for the synthesis of a novel class of glucocorticoid mimetics containing a trifluoromethyl-substituted alcohol // Bioorganic & Medicinal Chemistry Letters, 2006. V. 16. Iss. 3. P. 654-657.
Код: Выделить всё
http://dx.doi.org/10.1016/j.bmcl.2005.10.039
2. D. O'Hagan, N. A. Zaidi, R. B. Lamont The synthesis of (R)-γ-phenyl-γ-(trifluoromethyl) -butyrolactone and (2R,3S)-1,1,1-trifluoro-2-methoxy-2-phenyl-3,4-epoxybutane in homochiral forms // Tetrahedron: Asymmetry, 1993. V. 4. Iss. 7. P. 1703-1708.
Код: Выделить всё
http://dx.doi.org/10.1016/S0957-4166(00)80378-X
3. Brunhilde Voigt, Andrea Porzel, Dieter Golsch, Waldemar Adam and Günter Adam.
Regioselective oxyfunctionalization of brassinosteroids by methyl(trifluoromethyl) dioxirane: Synthesis of 25-hydroxy-brassinolide and 25-hydroxy-24-epibrassinolide by direct C-H insertion // Tetrahedron. Volume 52, Issue 32, 1996, Pages 10653-10658
Код: Выделить всё
http://dx.doi.org/10.1016/0040-4020(96)00587-X
4. Dmitry Zuev, Jodi A. Michne, Sokhom S. Pin, Jie Zhang, Matthew T. Taber and Gene M. Dubowchik. Optimization of CRF1R binding affinity of 2-(2,4,6-trichlorophenyl)-4-trifluoromethyl -5-aminomethylthiazoles through rapid and selective parallel synthesis // Bioorganic & Medicinal Chemistry Letters. Volume 15, Issue 2, 2005, Pages 431-434
Код: Выделить всё
http://dx.doi.org/10.1016/j.bmcl.2004.10.055
5. Margherita Moreno, Monica Sani, Guido Raos, Stefano V. Meille, Dorina Belotti, Raffaella Giavazzi, Stefano Bellosta, Alessandro Volonterio and Matteo Zanda. Stereochemically pure α-trifluoromethyl -malic hydroxamates: synthesis and evaluation as inhibitors of matrix metalloproteinases // Tetrahedron. Volume 62, Issue 43, 2006, Pages 10171-10181
Код: Выделить всё
http://dx.doi.org/10.1016/j.tet.2006.08.036
6. Hideto Fukui, Tetsuo Shibata, Takanobu Naito, Jun Nakano, Tetsuro Maejima, Hisato Senda, Wakao Iwatani, Yoshiyuki Tatsumi, Masahiro Suda and Ta-i Arika. Synthesis and antibacterial activity of novel 7-(3-substituted-3 or 4-trifluoromethyl -1-pyrrolidinyl)-8-methoxyfluoroquinolones. // Bioorganic & Medicinal Chemistry Letters. Volume 8, Issue 20, 1998, Pages 2833-2838
Код: Выделить всё
http://dx.doi.org/10.1016/S0960-894X(98)00514-9
7. Roberta Sinisi, Monica Sani, Gabriele Candiani, Rachele Parente, Françoise Pecker, Stefano Bellosta and Matteo Zanda.
Synthesis of α-trifluoromethyl -α-amino-β-sulfone hydroxamates: novel nanomolar inhibitors of matrix metalloproteinases
Tetrahedron Letters. Volume 46, Issue 38, 2005, Pages 6515-6518
Код: Выделить всё
http://dx.doi.org/10.1016/j.tetlet.2005.07.078
8. Anton V. Gulevich, Nikolay E. Shevchenko, Elisabeth S. Balenkova, Gerd-Volker Röschenthaler, and Valentine G. Nenajdenko.
The Ugi reaction with CF3-carbonyl compounds: effective synthesis of α-trifluoromethyl amino acid derivatives // Tetrahedron
Volume 64, Issue 51, 2008, Pages 11706-11712
Код: Выделить всё
http://dx.doi.org/10.1016/j.tet.2008.10.004
