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73. Zeng, Z. S.; Liang, Y. H.; Feng, X. Q.; Chen, F. E.; Pannecouque, C.; Balzarini, J.; De Clercq, E., Lead Optimization of Diarylpyrimidines as Non-nucleoside Inhibitors of HIV-1 Reverse Transcriptase. ChemMedChem 2010, 5 (6), 837-840.

72. Zeng, Z. S.; He, Q. Q.; Liang, Y. H.; Feng, X. Q.; Chen, F. E.; De Clercq, E.; Balzarini, J.; Pannecouque, C., Hybrid diarylbenzopyrimidine non-nucleoside reverse transcriptase inhibitors as promising new leads for improved anti-HIV-1 chemotherapy. Bioorganic & Medicinal Chemistry 2010, 18 (14), 5039-5047.

71. Xiong, F.; Chen, X. X.; Liu, Z. Q.; Chen, F. E., A novel synthetic strategy for the stereospecific total synthesis of (+/-)-biotin. Tetrahedron Letters 2010, 51 (28), 3670-3672.

70. Xiong, F.; Chen, X. X.; Chen, F. E., An improved asymmetric total synthesis of (+)-biotin via the enantioselective desymmetrization of a meso-cyclic anhydride mediated by cinchona alkaloid-based sulfonamide. Tetrahedron-Asymmetry 2010, 21 (6), 665-669.

69. Liang, Y. H.; He, Q. Q.; Zeng, Z. S.; Liu, Z. Q.; Feng, X. Q.; Chen, F. E.; Balzarini, J.; Pannecouque, C.; De Clercq, E., Synthesis and anti-HIV activity of 2-naphthyl substituted DAPY analogues as non-nucleoside reverse transcriptase inhibitors. Bioorganic & Medicinal Chemistry 2010, 18 (13), 4601-4605.

68. Kuang, Y. Y.; Niu, J. Z.; Chen, F. E., Synthetic Studies on Camptothecins Part 3 Total Synthesis of (20S)-7-Ethyl-10-hydroxycamptothecin via a Bifunctional Thiourea-Based Cinchona Alkaloid-Mediated Enantioselective Cyanosilylation Strategy. Helvetica Chimica Acta 2010, 93 (10), 2094-2099.

67. Huang, J. P.; Chen, X. X.; Gu, S. X.; Zhao, L.; Chen, W. X.; Chen, F. E., An Efficient Method for Removal of Residual Palladium from Organic Solution of Faropenem Sodium in the Pd(II)-Catalyzed Cleavage of Allyl Faropenem. Organic Process Research & Development 2010, 14 (4), 939-941.

66. Feng, X. Q.; Zeng, Z. S.; Liang, Y. H.; Chen, F. E.; Pannecouque, C.; Balzarini, J.; De Clercq, E., Synthesis and biological evaluation of 4-(hydroxyimino)arylmethyl diarylpyrimidine analogues as potential non-nucleoside reverse transcriptase inhibitors against HIV. Bioorganic & Medicinal Chemistry 2010, 18 (7), 2370-2374.

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