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Synthetic Communications
An International Journal for Rapid Communication of Synthetic Organic Chemistry
Volume 31, 2001 - Issue 12
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Original Articles

IMIDATION OF CYCLIC CARBOXYLIC ANHYDRIDES UNDER MICROWAVE IRRADIATION

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Pages 1927-1931 | Received 29 Aug 2000, Published online: 16 Aug 2006

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Joseph W. Rumer, Christine K.L. Hor, Iain Meager, Chin P. Yau, Zhenggang Huang, Christian B. Nielsen, Scott E. Watkins, Hugo Bronstein & Iain McCulloch. (2013) Alkyl side-chain branching point effects in thieno[3,4-c]pyrrole-4,6-dione copolymers. Journal of Organic Semiconductors 1:1, pages 30-35.
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Charles Goussu, Jean-Jacques Vasseur, Hervé Bazin & François Morvan. (2005) MICROWAVES SYNTHESIS OF SOLID SUPPORTS FOR THE SYNTHESIS OF 3′-AMINOALKYL OLIGODEOXYNUCLEOTIDES. Nucleosides, Nucleotides & Nucleic Acids 24:5-7, pages 623-627.
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Yanqing Peng, Gonghua Song & Ling Liu. (2004) SYNTHESIS OF 3-SUBSTITUTED-2-ACYLIMINO-4-THIAZOLIDONES UNDER MICROWAVE IRRADIATION. Organic Preparations and Procedures International 36:2, pages 151-155.
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Articles from other publishers (16)

Frank Betancourt, James Helmkay & Hongbin Yan. (2020) Microwave-Assisted Synthesis and Fluorescent Properties of 4-Phenyl-1,8-naphthalimide. Molbank 2020:2, pages M1127.
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Luxiao Liu, Hong-Yu Zhang, Guohui Yin, Yuecheng Zhang & Jiquan Zhao. (2019) Synthesis of N-unsubstituted cyclic imides from anhydride with urea in deep eutectic solvent (DES) choline chloride/urea. Chemical Papers 74:4, pages 1351-1357.
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R. Alan Aitken. 2019. Imides. Imides 1 28 .
Syed Sabir, Mansour Ibrahim Alhazza & Ahmed Aidid Ibrahim. (2016) A review on heterocyclic moieties and their applications. Catalysis for Sustainable Energy 2:1, pages 99-115.
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Xinhua Cao, Jing Zhou, Ying Zou, Mingming Zhang, Xudong Yu, Song Zhang, Tao Yi & Chunhui Huang. (2011) Fluorescence and Morphology Modulation in a Photochromic Diarylethene Self-Assembly System. Langmuir 27:8, pages 5090-5097.
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Pavel Kucheryavy, Guifeng Li, Shubham Vyas, Christopher Hadad & Ksenija D. Glusac. (2009) Electronic Properties of 4-Substituted Naphthalimides. The Journal of Physical Chemistry A 113:23, pages 6453-6461.
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Régis Barattin & André Gourdon. (2009) Synthesis of Two Complementary Molecular Moulds. European Journal of Organic Chemistry 2009:7, pages 1022-1026.
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Hiroshi Maruoka, Fumi Okabe, Yoshimichi Koutake, Toshihiro Fujioka & Kenji Yamagata. (2009) Diels-Alder Reaction of 2-(Cyclic Amino)-Substituted 3-Furancarbonitriles with Maleimides to Phthalimides. HETEROCYCLES 77:1, pages 617.
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Ellis Benjamin & Yousef Hijji. (2008) The Synthesis of Unsubstituted Cyclic Imides Using Hydroxylamine under Microwave Irradiation. Molecules 13:1, pages 157-169.
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Masaharu Uno, Hyun Seung Ban, Wataru Nabeyama & Hiroyuki Nakamura. (2008) de novo Design and synthesis of N-benzylanilines as new candidates for VEGFR tyrosine kinase inhibitors. Organic & Biomolecular Chemistry 6:6, pages 979.
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Ting-Yueh Tsai, Mohane Selvaraj Coumar, Tsu Hsu, Hsing-Pang Hsieh, Chia-Hui Chien, Chiung-Tong Chen, Chung-Nien Chang, Yu-Kang Lo, Ssu-Hui Wu, Chung-Yu Huang, Yu-Wen Huang, Min-Hsien Wang, Hsin-Yi Wu, Hong-Jen Lee, Xin Chen, Yu-Sheng Chao & Weir-Torn Jiaang. (2006) Substituted pyrrolidine-2,4-dicarboxylic acid amides as potent dipeptidyl peptidase IV inhibitors. Bioorganic & Medicinal Chemistry Letters 16:12, pages 3268-3272.
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Yousef M. Hijji & Ellis Benjamin. (2006) Efficient Microwave Assisted Syntheses of Unsubstituted Cyclic Imides. HETEROCYCLES 68:11, pages 2259.
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Manuela Rodriquez & Maurizio Taddei. 2006. Microwave-Assisted Synthesis of Heterocycles. Microwave-Assisted Synthesis of Heterocycles 213 266 .
Annalisa Mortoni, Marisa Martinelli, Umberto Piarulli, Nickolas Regalia & Stefania Gagliardi. (2004) Microwave-assisted solvent-free synthesis of a quinoline-3,4-dicarboximide library on inorganic solid supports. Tetrahedron Letters 45:35, pages 6623-6627.
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Michael B. Smith. 2003. Compendium of Organic Synthetic Methods. Compendium of Organic Synthetic Methods 226 263 .
Yanqing Peng, Gonghua Song & Xuhong Qian. (2010) ChemInform Abstract: Imidation of Cyclic Carboxylic Anhydrides under Microwave Irradiation.. ChemInform 32:48.
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