Pure and Applied Chemistry

CrossRef Cited-by Linking

• Ishihara Yoshihiro, Mendoza Abraham, Baran Phil S.: Total synthesis of taxane terpenes: cyclase phase. Tetrahedron 2013, 69, 5685. <http://dx.doi.org/10.1016/j.tet.2013.04.028>
• FALLIS A. G.: ChemInform Abstract: From Tartrate to Taxoids: A Double, Intramolecular Diels-Alder Strategy. ChemInform 2010, 28, no. <http://dx.doi.org/10.1002/chin.199728237>
• Sun Youmin, Chen Dezhan, Liu Chengbu, Yang Zuoyin, Xu Xiufang, Wang Guichang, Shang Zhenfeng, Cai Zunsheng, Pan Yinming, Zhao Xuezhuang, Vijaya R, Sastry G.Narahari: Evaluation of the effectiveness of AM1 geometry used in calculating O���H bond dissociation enthalpy. Journal of Molecular Structure: THEOCHEM 2002, 618, 181. <http://dx.doi.org/10.1016/S0166-1280(02)00405-0>
• Martin Catherine, Macintosh Nicole, Lamb Nancy, Fallis Alex G.: Benzobicyclo[8.4.0.^1,60^8,13]tetradecenones:  Ring CD-Taxoid Models by Planar Tether Controlled Cycloaddition. Org Lett 2001, 3, 1021. <http://dx.doi.org/10.1021/ol015559y>
• Fallis Alex G, Forgione Pat, Woo Simon, Legoupy Stephanie, Py Sandrine, Harwig Curtis, Rietveld Tanya: Organometallic reagents and protocols for synthesis. J Polyhedron 2000, 19, 533. <http://dx.doi.org/10.1016/S0277-5387(99)00402-7>
• Melekhov Alex, Forgione Pat, Legoupy Stéphanie, Fallis Alex G.: Tether-Controlled Cycloadditions for the Asymmetric Synthesis of Decalins:  Increased Selectivity in Acetonitrile Solvent. Org Lett 2000, 2, 2793. <http://dx.doi.org/10.1021/ol0062042>
• Comanita Bogdan M., Heuft Matthew A., Rietveld Tanya, Fallis Alex G.: A mild route to α-alkoxyacetylenes mediated by lewis acids and synthetic routes to 10-, 11-, and 12-membered ring enediyne carbocycles. Isr J Chem 2000, 40, 241. <http://dx.doi.org/10.1560/7J4F-D8BG-3FQR-E3TD>
• P. Dell Colin: Cycloadditions in synthesis. J Chem Soc Perkin Trans 1 1998, 3873. <http://dx.doi.org/10.1039/a803583k>
• Wong Timothy, Wilson Peter D., Woo Simon, Fallis Alex G.: Isopropylidene acetals: Tether control groups for asymmetric intramolecular Diels-Alder reactions. Tetrahetron Lett 1997, 38, 7045. <http://dx.doi.org/10.1016/S0040-4039(97)01708-5>