Pure and Applied Chemistry

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• Hsieh Pei-Wen, Wu Jin-Bin, Wu Yang-Chang: Chemistry and biology of Phellinus linteus. BioMedicine 2013, 3, 106. <http://dx.doi.org/10.1016/j.biomed.2013.01.002>
• Karunamoorthi Kaliyaperumal, Sabesan Shanmugavelu, Jegajeevanram Kaliyaperumal, Vijayalakshmi Jayaraman: Role of Traditional Antimalarial Plants in the Battle Against the Global Malaria Burden. Vector-Borne and Zoonotic Diseases 2013, 13, 521. <http://dx.doi.org/10.1089/vbz.2011.0946>
• Hwang Min Woo, Lee Hee Jung, Song Ho Joon, Kim Byung Joo: Involvement of MAPKs and PLC Pathways in Modulation of Pacemaking Activity by So-Cheong-Ryong-Tang in Interstitial Cells of Cajal from Murine Small Intestine. The Scientific World Journal 2013, 2013, 1. <http://dx.doi.org/10.1155/2013/536350>
• Hassan Haider M., Jiang Zi-Hua, Syed Tarannum A., Qin Wensheng: Review: Northern Ontario medicinal plants. Can. J. Plant Sci. 2012, 92, 815. <http://dx.doi.org/10.4141/cjps2012-006>
• BAI D.: ChemInform Abstract: Traditional Chinese Medicines and New Drug Development. ChemInform 2010, 24, no. <http://dx.doi.org/10.1002/chin.199336307>
• Pan Qiang-Biao, Ma Da-Wei: Chiral Guanidine Catalyzed Annulation to the Core Structure of (-)-Huperzine A. Chin J Chem 2010, 21, 793. <http://dx.doi.org/10.1002/cjoc.20030210716>
• Özçelik Berrin, Aslan Sinem, Kartal Murat, Karaoglu Taner, Şener Bilge, Terzioglu Salih, Choudhary M. Iqbal, Orhan Ilkay: Antioxidant and antimicrobial actions of the clubmoss Lycopodium clavatum L. Phytochem Rev 2007, 6, 189. <http://dx.doi.org/10.1007/s11101-006-9053-x>
• Orhan Ilkay, Küpeli Esra, Şener Bilge, Yesilada Erdem: Appraisal of anti-inflammatory potential of the clubmoss, Lycopodium clavatum L. Journal of Ethanopharmacology 2007, 109, 146. <http://dx.doi.org/10.1016/j.jep.2006.07.018>
• Zhou Mei, Liu Yang, Chen Tianbao, Fang Xuexun, Walker Brian, Shaw Chris: Components of the peptidome and transcriptome persist in lin wa pi: The dried skin of the Heilongjiang brown frog (Rana amurensis) as used in traditional Chinese medicine. Peptides (Fayetteville) 2006, 27, 2688. <http://dx.doi.org/10.1016/j.peptides.2006.05.009>
• Choi Lee Ihl Young, Hong Joong Yeoun, Jung Myung Hee, Lee Hyo Won: Synthesis of huperzine B through ring closing metathesis. Tetrahetron Lett 2004, 45, 285. <http://dx.doi.org/10.1016/j.tetlet.2003.10.169>
• Bello-Ramirez Angelica M., Nava-Ocampo Alejandro A.: The local anesthetic activity of Aconitum alkaloids can be explained by their structural properties: a QSAR analysis. Fundam Clin Pharmacol 2004, 18, 157. <http://dx.doi.org/10.1111/j.1472-8206.2004.00222.x>
• Bello-Ramirez Angelica M., Buendia-Orozco Jacob, Nava-Ocampo Alejandro A.: A QSAR analysis to explain the analgesic properties of Aconitum alkaloids. Fundam Clin Pharmacol 2003, 17, 575. <http://dx.doi.org/10.1046/j.1472-8206.2003.00189.x>
• Lee Ihl Young Choi, Jung Myung Hee, Lee Hyo Won, Yang Joon Youn: Synthesis of huperzine intermediates via Mn(III)-mediated radical cyclization. Tetrahetron Lett 2002, 43, 2407. <http://dx.doi.org/10.1016/S0040-4039(02)00270-8>
• Camps Pelayo, Muñoz-Torrero Diego, Simon Montserrat: EASY ACCESS TO 4-SUBSTITUTED (±)-HUPERZINE A ANALOGUES. Synth Common 2001, 31, 3507. <http://dx.doi.org/10.1081/SCC-100106212>
• Carlier Paul R., Du Da-Ming, Han Yi-Fan, Liu Jing, Perola Emanuele, Williams Ian D., Pang Yuan-Ping: Dimerization of an Inactive Fragment of Huperzine A Produces a Drug with Twice the Potency of the Natural Product. Angew Chem 2000, 112, 1845. <http://dx.doi.org/10.1002/(SICI)1521-3757(20000515)112:10<1845::AID-ANGE1845>3.0.CO;2-S>
• Camps Pelayo, Contreras Joan, El Achab Rachid, Morral Jordi, Muñoz-Torrero Diego, Font-Bardia Mercè, Solans Xavier, Badia Albert, Vivas Nuria M: New Syntheses of rac-Huperzine A and its rac-7-Ethyl-Derivative. Evaluation of Several Huperzine A Analogues as Acetylcholinesterase Inhibitors. Tetrahedron 2000, 56, 4541. <http://dx.doi.org/10.1016/S0040-4020(00)00363-X>
• Ling Y.-C, Teng H.-C, Cartwright C: Supercritical fluid extraction and clean-up of organochlorine pesticides in Chinese herbal medicine. J Chromatogr A 1999, 835, 145. <http://dx.doi.org/10.1016/S0021-9673(98)01077-2>
• Camps Pelayo, Contreras Joan, Morral Jordi, Muñoz-Torrero Diego, Font-Bardia Mercè, Solans Xavier: Synthesis of an 11-unsubstituted analogue of (±)-huperzine A. Tetrahedron 1999, 55, 8481. <http://dx.doi.org/10.1016/S0040-4020(99)00434-2>
• Chassaing Christophe, Haudrechy Arnaud, Langlois Yves: Asymmetric palladium annulation: formal synthesis of (+)-huperzine A. Tetrahetron Lett 1999, 40, 8805. <http://dx.doi.org/10.1016/S0040-4039(99)01874-2>
• Kaneko Satoru, Yoshino Toshiharu, Katoh Tadashi, Terashima Shiro: Synthetic studies of huperzine A and its fluorinated analogues. 1. Novel asymmetric syntheses of an enantiomeric pair of huperzine A. Tetrahedron 1998, 54, 5471. <http://dx.doi.org/10.1016/S0040-4020(98)00227-0>
• Kaneko Satoru, Nakajima Noriyuki, Shikano Mayumi, Katoh Tadashi, Terashima Shiro: Synthetic studies of huperzine A and its fluorinated analogues. 2. Synthesis and acetylcholinesterase inhibitory activity of novel fluorinated huperzine A analogues. Tetrahedron 1998, 54, 5485. <http://dx.doi.org/10.1016/S0040-4020(98)00228-2>
• He Xu-Chang, Wang Bin, Bai Donglu: Studies on asymmetric synthesis of hyperzine A 1. Palladium-catalyzed asymmetric bicycloannulation of 5,6,7,8-tetrahydro-2-methoxy-6-oxo-5-quinolinecarboxylic esters. Tetrahetron Lett 1998, 39, 411. <http://dx.doi.org/10.1016/S0040-4039(97)10535-4>
• Da-Yuan Zhu, Dong-Lu Bai, Xi-Can Tang: Recent studies on traditional Chinese medicinal plants. Drug Dev Res 1996, 39, 147. <http://dx.doi.org/10.1002/(SICI)1098-2299(199610)39:2<147::AID-DDR6>3.0.CO;2-P>
• Kaneko Satoru, Nakajima Noriyuki, Shikano Mayumi, Katoh Ta-i, Terashima Shiro: Synthesis and acetylcholinesterase inhibitory activity of fluorinated analogues of huperzine A. Biorg Med Chem Lett 1996, 6, 1927. <http://dx.doi.org/10.1016/0960-894X(96)00337-X>
• Zhu Da-Yuan, Jiang Shang-Hao, Huang Mei-Fen, Lin Long-Ze, Cordell Geoffrey A.: Huperserratinine from Huperzia serrata. Phytochemisry 1994, 36, 1069. <http://dx.doi.org/10.1016/S0031-9422(00)90493-X>