Z. Hayouka, M. Hurevich, A. Levin, H. Benyamini, A. Iosub, M. Maes, D. E. Shalev, A. Loyter, C. Gilon, and A. Friedler. 2010. “Cyclic peptide inhibitors of HIV-1 integrase derived from the LEDGF/p75 protein.” Bioorganic & Medicinal Chemistry, 18, 23, Pp. 8388-8395. Publisher's Version
M. Hurevich, Y. Tal-Gan, S. Klein, Y. Barda, A. Levitzki, and C. Gilon. 2010. “Novel method for the synthesis of urea backbone cyclic peptides using new Alloc-protected glycine building units.” Journal of Peptide Science, 16, 4, Pp. 178-185. Publisher's Version
M. Hurevich, A. Swed, S. Joubran, S. Cohen, N. S. Freeman, E. Britan-Rosich, L. Briant-Longuet, M. Bardy, C. Devaux, M. Kotler, A. Hoffman, and C. Gilon. 2010. “Rational conversion of noncontinuous active region in proteins into a small orally bioavailable macrocyclic drug-like molecule: The HIV-1 CD4:gp120 paradigm.” Bioorganic & Medicinal Chemistry, 18, 15, Pp. 5754-5761. Publisher's Version
N. S. Freeman, M. Hurevich, and C. Gilon. 2009. “Synthesis of N '-substituted Ddz-protected hydrazines and their application in solid phase synthesis of aza-peptides.” Tetrahedron, 65, 8, Pp. 1737-1745. Publisher's Version
F. Nuti, N. Qvit, F. Rizzolo, M. Hurevich, A. Carotenuto, E. Peroni, M. Chelli, R. Paolo, G. Chaim, and A. M. Papini. 2008. “Microwave-assisted solid phase synthesis of backbone cyclic glycopeptide libraries.” Journal of Peptide Science, 14, 8, Pp. 131-131. Publisher's Version
N. S. Freeman, M. Hurevich, and C. Gilon. 2008. “Solid phase synthesis of azapeptides using activated N beta ss (TM)-Substituted ddz protected hydrazines.” Journal of Peptide Science, 14, 8, Pp. 66-66. Publisher's Version
M. Hurevich, Y. Barda, and C. Gilon. 2007. “Synthesis of novel urea bridged macrocyclic molecules using BTC.” Heterocycles, 73, 1, Pp. 617-+. Publisher's Version
M. Hurevich, Y. Barda, and C. Gilon. 2004. “On-Resin Urea Cyclization of Diamines Using Triphosgene.” Journal of Peptide Science, 10, Pp. 127-127. Publisher's Version