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Synthetic Communications
An International Journal for Rapid Communication of Synthetic Organic Chemistry
Volume 37, 2007 - Issue 1
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Original Articles

L‐Proline‐Catalyzed Michael Addition of Aldehydes and Unmodified Ketones to Nitro Olefins Accelerated by Et3N

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Pages 91-98 | Received 17 May 2006, Published online: 25 Jul 2007

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SwapnilR. Sarda, WamanraoN. Jadhav, AmitS. Shete, KiranB. Dhopte, SachinM. Sadawarte, PrashantJ. Gadge & RajendraP. Pawar. (2010) Phosphonium Ionic Liquid–Catalyzed Michael Addition of Mercaptans to α,β-Unsaturated Ketones. Synthetic Communications 40:14, pages 2178-2184.
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Tapaswini Das, Seetaram Mohapatra, Nilima P. Mishra, Sabita Nayak & Bishnu P. Raiguru. (2021) Recent Advances in Organocatalytic Asymmetric Michael Addition Reactions to α, β‐Unsaturated Nitroolefins. ChemistrySelect 6:15, pages 3745-3781.
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Hanbin Lu, Jiamin Lv, Canhua Zhou, Mi Zhou, Yanxiong Fang, Jinxiang Dong, Terumasa Kato, Yan Liu & Keiji Maruoka. (2021) Remarkable Effect of tert ‐Amine Additives in the Asymmetric Direct Michael Reaction of Ketones with β‐Arylnitroethenes Catalyzed by an L ‐Hydroxyproline‐Based Amino Tf‐Amide Organocatalyst . European Journal of Organic Chemistry 2021:12, pages 1909-1912.
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Alan Armstrong & Paul Dingwall. 2016. Lewis Base Catalysis in Organic Synthesis. Lewis Base Catalysis in Organic Synthesis 145 190 .
Han Yu, Mouming Liu & Sheng Han. (2014) Highly efficient asymmetric Michael addition of aldehydes to nitroalkenes with 4,5-methano-l-proline as organocatalysts. Tetrahedron 70:44, pages 8380-8384.
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Zhi-Hua Yu, Hu-Fei Zheng, Wei Yuan, Zi-Long Tang, Ai-Dong Zhang & De-Qing Shi. (2013) An unexpected one-pot synthesis of multi-substituted quinolines via a cascade reaction of Michael/Staudinger/aza-Wittig/aromatization of ortho-azido-β-nitro-styrenes with various carbonyl compounds. Tetrahedron 69:38, pages 8137-8141.
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Kun Xu, Sheng Zhang, Yanbin Hu, Zhenggen Zha & Zhiyong Wang. (2013) Asymmetric Michael Reaction Catalyzed by Proline Lithium Salt: Efficient Synthesis of L ‐Proline and Isoindoloisoquinolinone Derivatives . Chemistry – A European Journal 19:11, pages 3573-3578.
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Zong-Bo Xie, Na Wang, Ming-Yu Wu, Ting He, Zhang-Gao Le & Xiao-Qi Yu. (2012) Catalyst-free and solvent-free Michael addition of 1,3-dicarbonyl compounds to nitroalkenes by a grinding method. Beilstein Journal of Organic Chemistry 8, pages 534-538.
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Shu‐rong Ban, Hong‐yu Xie, Xi‐xia Zhu & Qing‐shan Li. (2011) Highly Enantioselective Michael Addition of Ketones to Nitroolefins with a Pyrrolidine‐Based Phthalimide as an Enamine‐Type Organocatalyst. European Journal of Organic Chemistry 2011:32, pages 6413-6417.
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Thomas C. Nugent, Mohammad Shoaib & Amna Shoaib. (2011) Practical access to highly enantioenriched quaternary carbon Michael adducts using simple organocatalysts. Org. Biomol. Chem. 9:1, pages 52-56.
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Zerong Wang. 2010. Comprehensive Organic Name Reactions and Reagents. Comprehensive Organic Name Reactions and Reagents 1922 1928 .
Matthias Freund, Sebastian Schenker & Svetlana B. Tsogoeva. (2009) Enantioselective nitro-Michael reactions catalyzed by short peptides on water. Organic & Biomolecular Chemistry 7:20, pages 4279.
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Markus Wiesner, Jefferson D. Revell & Helma Wennemers. (2008) Tripeptides as Efficient Asymmetric Catalysts for 1,4‐Addition Reactions of Aldehydes to Nitroolefins–A Rational Approach. Angewandte Chemie International Edition 47:10, pages 1871-1874.
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Markus Wiesner, Jefferson D. Revell & Helma Wennemers. (2008) Tripeptides as Efficient Asymmetric Catalysts for 1,4‐Addition Reactions of Aldehydes to Nitroolefins–A Rational Approach. Angewandte Chemie 120:10, pages 1897-1900.
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Hiyoshizo Kotsuki, Hideaki Ikishima & Atsushi Okuyama. (2008) Organocatalytic Asymmetric Synthesis Using Proline and Related Molecules. Part 2.. HETEROCYCLES 75:4, pages 757.
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P. Kočovskí. 2007. Organic Reaction Mechanisms · 2007. Organic Reaction Mechanisms · 2007 275 337 .
B. M. Choudary, Ch. V. Rajasekhar, G. Gopi Krishna & K. Rajender Reddy. (2007) L‐Proline‐Catalyzed Michael Addition of Aldehydes and Unmodified Ketones to Nitro Olefins Accelerated by Et 3 N. . ChemInform 38:25.
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