Pure and Applied Chemistry

CrossRef Cited-by Linking

• Huang Aiping, Qiao Zhi, Zhang Xinhai, Yu Wei, Zheng Qingqing, Ma Ying, Ma Chen: A transition metal-free tandem process to pyrrolopyrazino[2,3-d]pyridazine-diones. Tedrahedron 2012, 68, 906. <http://dx.doi.org/10.1016/j.tet.2011.11.021>
• Martinelli Jonathan, Gugliotta Giuseppe, Tei Lorenzo: Synthesis of 6-Substituted 6-Nitroperhydro-1,4-diazepines via Novel Tandem Retro-Henry and Mannich/Michael Reactions. Org Lett 2012, 14, 716. <http://dx.doi.org/10.1021/ol203101s>
• Gong Jian, Xie Fuchun, Ren Wenming, Chen Hong, Hu Youhong: Domino reactions of 2-methyl chromones containing an electron withdrawing group with chromone-fused dienes. Biomol Chem 2012, 10, 486. <http://dx.doi.org/10.1039/c1ob06613g>
• Song Zhen-Lei, Fan Chun-An, Tu Yong-Qiang: Semipinacol Rearrangement in Natural Product Synthesis. Chemistry Review 2011, 111, 7523. <http://dx.doi.org/10.1021/cr200055g>
• Hájíček Josef: Recent developments in syntheses of the post-secodine indole alkaloids. Part III: Rearranged alkaloid types. Collection Czech Chem Commun 2011, 76, 2023. <http://dx.doi.org/10.1135/cccc2011099>
• Anastas Paul, Eghbali Nicolas: Green Chemistry: Principles and Practice. Chem Soc Rev 2010, 39, 301. <http://dx.doi.org/10.1039/b918763b>
• Tadano Kin-ichi: Natural Product Synthesis Featuring Intramolecular Diels-Alder Approaches - Total Syntheses of Tubelactomicins and Spiculoic Acid A. Eur J Org Chem 2009, 2009, 4381. <http://dx.doi.org/10.1002/ejoc.200900409>
• Bonfield E. Ryan, Li Chao-Jun: Efficient Preparation of the Isoindoline Frameworkvia a Six Component, Tandem Double A3-Coupling and [2+2+2] Cycloaddition Reaction. Adv Synth Catal 2008, 350, 370. <http://dx.doi.org/10.1002/adsc.200700500>
• Dadwal Mamta, Kesharwani Manoj K., Danayak Vaishalee, Ganguly Bishwajit, Mobin Shaikh M., Muruganantham Rajendran, Namboothiri Irishi N. N.: Synthetic and Theoretical Investigations on the Construction of Oxanorbornenes by a Michael Addition and Intramolecular Diels-Alder Furan Reaction. Eur J Org Chem 2008, 2008, 6106. <http://dx.doi.org/10.1002/ejoc.200800681>
• Mejía-Oneto José M., Padwa Albert: Total Synthesis of the Alkaloid (±)-Aspidophytine Based on Carbonyl Ylide Cycloaddition Chemistry. HCA 2008, 91, 285. <http://dx.doi.org/10.1002/hlca.200890034>
• Guillena Gabriela, Ramón Diego J., Yus Miguel: Organocatalytic enantioselective multicomponent reactions (OEMCRs). Tet Asymm 2007, 18, 693. <http://dx.doi.org/10.1016/j.tetasy.2007.03.002>
• Hájíček Josef: A Review on Recent Developments in Syntheses of the post-Secodine Indole Alkaloids. Part II: Modified Alkaloid Types. Collect Czech Chem Commun 2007, 72, 821. <http://dx.doi.org/10.1135/cccc20070821>
• Nicolaou K. C., Edmonds David J., Bulger Paul G.: Kaskadenreaktionen in der Totalsynthese. Angew Chem 2006, 118, 7292. <http://dx.doi.org/10.1002/ange.200601872>
• Nicolaou K. C., Edmonds David J., Bulger Paul G.: Cascade Reactions in Total Synthesis. Angew Chem Int Ed 2006, 45, 7134. <http://dx.doi.org/10.1002/anie.200601872>
• Nikolaev Vsevolod V., Heimgartner Heinz, Linden Anthony, Krylov Ivan S., Nikolaev Valerij A.: RhII-Catalyzed Reactions of Diazocarbonyl Compounds with Dicarboximides. Eur J Org Chem 2006, 2006, 4737. <http://dx.doi.org/10.1002/ejoc.200600396>
• Nikolaev Vsevolod, Hennig Lothar, Heimgartner Heinz, Schulze Barbel, Nikolaev Valerij: Dual reactivity of imidic carbonyl ylides in Rh(II)-catalyzed reactions of α-diazocarbonyl compounds with succinimide. Tetrahetron Lett 2006, 47, 2643. <http://dx.doi.org/10.1016/j.tetlet.2006.01.155>
• Herdeis Claus, Küpper Patrick, Plé Sophie: An expeditious stereoselective synthesis of natural (–)-Cassine via cascade HWE [3 + 2]-cycloaddition process. Org Biomol Chem 2006, 4, 524. <http://dx.doi.org/10.1039/b516888k>
• Laleu Beno?t, Machado Marco Santarem, Lacour J?r?me: Pummerer fragmentation vs. Pummerer rearrangement: a mechanistic analysis. Chem Commun 2006, 2786. <http://dx.doi.org/10.1039/b605187a>
• Padwa Albert: Tandem Methodology for Heterocyclic Synthesis. ChemInform 2005, 36. <http://dx.doi.org/10.1002/chin.200520273>