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Usp. Khim., 2011, Volume 80, Issue 3, Pages 211–232 (Mi rcr45)  

This article is cited in 81 scientific papers (total in 81 papers)

Aza-Michael reaction: achievements and prospects

A. Yu. Rulev

A. E. Favorsky Irkutsk Institute of Chemistry, Siberian Branch of the Russian Academy of Sciences

Abstract: Data published in the last 10 years on the use of the aza-Michael reaction in organic synthesis are described systematically. The attention is focused on environmentally friendly processes following green chemistry principles and on methods for the synthesis of compounds that are difficult to access by other routes.

Full text: http://www.uspkhim.ru/.../paper_rus.phtml?journal_id=rc&paper_id=4162

English version:
Russian Chemical Reviews, 2011, 80:3, 197–218

Bibliographic databases:

Document Type: Article
Received: 20.05.2010

Citation: A. Yu. Rulev, “Aza-Michael reaction: achievements and prospects”, Usp. Khim., 80:3 (2011), 211–232; Russian Chem. Reviews, 80:3 (2011), 197–218

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  • http://mi.mathnet.ru/eng/rcr/v80/i3/p211

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    Citing articles on Google Scholar: Russian citations, English citations
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    4. Liyan Dai, Yi Zhang, Qianqian Dou, Xiaozhong Wang, Yingqi Chen, “Chemo/Regioselective Aza-Michael additions of amines to conjugate alkenes catalyzed by polystyrene-supported AlCl3”, Tetrahedron, 2012  crossref  isi  scopus
    5. Gloria Martinez, Jayanthi Arumugam, Hollie K. Jacobs, Aravamudan S. Gopalan, “3,2-Hydroxypyridinone (3,2-HOPO) vinyl sulfonamide and acrylamide linkers: aza-Michael addition reactions and the preparation of poly-HOPO chelators”, Tetrahedron Letters, 2012  crossref  isi  scopus
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