Pure and Applied Chemistry

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• He Chi, Zhu Chenlong, Dai Zhifeng, Tseng Chih-Chung, Ding Hanfeng: Divergent Total Synthesis of Indoxamycins A, C, and F. Angew. Chem. 2013, 125, 13498. <http://dx.doi.org/10.1002/ange.201307426>
• He Chi, Zhu Chenlong, Dai Zhifeng, Tseng Chih-Chung, Ding Hanfeng: Divergent Total Synthesis of Indoxamycins A, C, and F. Angew. Chem. Int. Ed. 2013, 52, 13256. <http://dx.doi.org/10.1002/anie.201307426>
• Jalli Venkata Prasad, Jaggavarapu Satyanarayana Reddy, Kamalakaran Anand Solomon, Gangisetty Sravan Kumar, Nanubolu Jagadeesh Babu, Gaddamanugu Gopikrishna: Direct access to novel chromeno-pyrimidine-N-oxides via tandem base catalyzed double nucleophilic addition/dehydration reaction. Tetrahedron Letters 2013, 54, 1491. <http://dx.doi.org/10.1016/j.tetlet.2013.01.044>
• Xu Xinfang, Zavalij Peter Y., Hu Wenhao, Doyle Michael P.: Vinylogous Reactivity of Enol Diazoacetates with Donor–Acceptor Substituted Hydrazones. Synthesis of Substituted Pyrazole Derivatives. J. Org. Chem. 2013, 78, 1583. <http://dx.doi.org/10.1021/jo302696y>
• Niu Xiaoyi, Yang Bingchuan, Li Yanqiu, Fang Shuai, Huang Zixiao, Xie Caixia, Ma Chen: A transition metal-free tandem process to pyridazinopyrido[3,2-f][1,4]thiazepine-diones via Smiles rearrangement. Org. Biomol. Chem. 2013, 11, 4102. <http://dx.doi.org/10.1039/c3ob40719e>
• Jha Amitabh, Naidu Ajaya B., Abdelkhalik Ashraf M.: Transition metal-free one-pot cascade synthesis of 7-oxa-2-azatricyclo[7.4.0.02,6]trideca-1(9),10,12-trien-3-ones from biomass-derived levulinic acid under mild conditions. Org. Biomol. Chem. 2013, 11, 7559. <http://dx.doi.org/10.1039/c3ob41826j>
• Mishra Priya, Singh Sarita, Ankit Preyas, Fatma Shahin, Singh Divya, Singh Jagdamba: Novel Synthesis of 3-Phenyl-chromen-4-ones Using N-Heterocyclic Carbene as Organocatalyst: An Efficient Domino Catalysis Type Approach. Bulletin of the Korean Chemical Society 2013, 34, 1070. <http://dx.doi.org/10.5012/bkcs.2013.34.4.1070>
• 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>
• Downey C. Wade, Craciun Smaranda, Vivelo Christina A., Neferu Ana M., Mueller Carly J., Corsi Stephanie: One-pot three-step thioconjugate addition-oxidation-Diels–Alder reactions of ethyl propiolate. Tetrahedron Letters 2012, 53, 5766. <http://dx.doi.org/10.1016/j.tetlet.2012.08.054>
• 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>
• Gembus Vincent, Bonfanti Jean-François, Querolle Olivier, Jubault Philippe, Levacher Vincent, Hoarau Christophe: Palladium Catalyzed One-Pot Sequential Suzuki Cross-Coupling–Direct C–H Functionalization of Imidazo[1,2-a]pyrazines. Org. Lett. 2012, 14, 6012. <http://dx.doi.org/10.1021/ol3029059>
• 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>
• Hong Xuechuan, France Stefan, Padwa Albert: A dipolar cycloaddition approach toward the kopsifoline alkaloid framework. Tetrahedron 2007, 63, 5962. <http://dx.doi.org/10.1016/j.tet.2007.01.064>
• 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>