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Synthetic Communications
An International Journal for Rapid Communication of Synthetic Organic Chemistry
Volume 35, 2005 - Issue 13
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Original Articles

Synthesis of Novel Spiroheterocyclic Framework via the Regioselective 1,3‐Dipolar Cycloaddition Reaction of Azomethine Ylides

Xiao‐Fen Hu Department of Fine Chemicals, School of Chemical Engineering, Tianjin University, Tianjin, China
&
Ya‐Qing Feng Department of Fine Chemicals, School of Chemical Engineering, Tianjin University, Tianjin, ChinaCorrespondence[email protected]
Pages 1747-1752 | Received 16 Mar 2005, Published online: 15 Aug 2006

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Reza Heydari, Batool Tahamipour, Niloofar Akbarzadeh Torbati, Claudia Graiff & Morteza Ziyaadini. (2013) One-Pot Synthesis and X-Ray Structure of New, Stable Tetrahydropyrrolo [1,2-a][1,10]phenanthrolines with Four Diastereoisomeric Centers. Synthetic Communications 43:15, pages 2031-2041.
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Articles from other publishers (9)

Xuemin Li, Huiyuan Liang, Yaxin O Yang, Xi Wang, Jingran Zhang, Donghua Wang, Fengxia Sun & Yunfei Du. (2020) Synthesis of Spiro[benzofuran‐2,2'‐benzo[ b ]thiophene]‐3,3'‐diones via PIDA/CuBr‐Mediated Spirocyclization . European Journal of Organic Chemistry 2020:42, pages 6563-6569.
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Jun Yang, Xiong-Wei Liu, Dan-Dan Wang, Min-Yi Tian, Shuo-Nan Han, Ting-Ting Feng, Xiong-Li Liu, Ren-Qiang Mei & Ying Zhou. (2016) Diversity-oriented one-pot multicomponent synthesis of spirooxindole derivatives and their biological evaluation for anticancer activities. Tetrahedron 72:52, pages 8523-8536.
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Xiong-Li Liu, Ting-Ting Feng, Wei-Dong Jiang, Chao Yang, Min-Yi Tian, Yan Jiang, Bing Lin, Zhi Zhao & Ying Zhou. (2016) Molecular hybridization-guided 1,3-dipolar cycloaddition reaction enabled pyrimidine-fused spiropyrrolidine oxindoles synthesis as potential anticancer agents. Tetrahedron Letters 57:39, pages 4411-4416.
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Xiong-Li Liu, Chao Yang, Wen-Hui Zhang, Gen Zhou, Xi-Tao Ma, Bing Lin, Min Zhang, Ying Zhou & Ting-Ting Feng. (2016) Construction of turmerone motif-fused spiropyrrolidine oxindoles and their biological evaluation for anticancer activities. Tetrahedron Letters 57:12, pages 1385-1389.
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Qin Xu, De Wang, Yin Wei & Min Shi. (2014) Highly Efficient and Stereoselective Construction of Bispirooxindole Derivatives via a Three‐Component 1,3‐Dipolar Cycloaddition Reaction. ChemistryOpen 3:3, pages 93-98.
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A. A. Shvets & S. V. Kurbatov. (2012) Synthesis of bis-β,β′-spiro-pyrrolidinyl-oxindoles, containing a rhodanine fragment. Chemistry of Heterocyclic Compounds 48:5, pages 799-806.
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Mahalingam Poornachandran & Ragavachary Raghunathan. (2006) Synthesis of dispirooxindolecycloalka[d]pyrimidino[2,3-b]-thiazole pyrrolidine/thiapyrrolizidine ring systems. Tetrahedron 62:48, pages 11274-11281.
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Ronald Grigg & Mohammed Abul Basher Sarker. (2006) XY–ZH compounds as potential 1,3-dipoles. Part 63: Silver catalysed azomethine ylide cycloaddition—the synthesis of spiro homoserine lactone analogues. Tetrahedron 62:44, pages 10332-10343.
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Xiao‐Fen Hu & Ya‐Qing Feng. (2005) Synthesis of Novel Spiroheterocyclic Framework via the Regioselective 1,3‐Dipolar Cycloaddition Reaction of Azomethine Ylides.. ChemInform 36:46.
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