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Mendeleev Communications, 2012, Volume 22, Issue 2, Pages 90–91
DOI: https://doi.org/10.1016/j.mencom.2012.03.013
(Mi mendc2750)
 

This article is cited in 5 scientific papers (total in 5 papers)

[3 + 2]-Cycloaddition of azomethine ylide at 1,3-dimethyl-6-(2-oxo-1,2-dihydro-3H-indol-3-ylidene)-3a,9a-diphenyl-3,3a,9,9a-tetrahydroimidazo[4,5-e][1,3]thiazolo[3,2-b][1,2,4]triazine-2,7(1H,6H)-diones

A. N. Kravchenkoa, P. A. Poluboyarova, S. V. Vasilevskiia, G. A. Gazievaa, Yu. V. Nelyubinab

a N.D. Zelinsky Institute of Organic Chemistry, Russian Academy of Sciences, Moscow, Russian Federation
b A.N. Nesmeyanov Institute of Organoelement Compounds of Russian Academy of Sciences, Moscow, Russian Federation
Full-text PDF (295 kB) Citations (5)
Abstract: [3 + 2]-Cycloaddition of azomethine ylide generated from formaldehyde and sarcosine at the double bond of 1,3-dimethyl-6-(2-oxo-1,2-dihydro-3H-indol-3-ylidene)-3a,9a-diphenyl-3,3a,9,9a-tetrahydroimidazo[4,5e][1,3]thiazolo[3,2-b][1,2,4]triazine-2,7(1H,6H)-diones occurs stereospecifically at the face opposite to the phenyl substituents. Product 3a crystallizes as a conglomerate.
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Document Type: Article
Language: English


Citation: A. N. Kravchenko, P. A. Poluboyarov, S. V. Vasilevskii, G. A. Gazieva, Yu. V. Nelyubina, “[3 + 2]-Cycloaddition of azomethine ylide at 1,3-dimethyl-6-(2-oxo-1,2-dihydro-3H-indol-3-ylidene)-3a,9a-diphenyl-3,3a,9,9a-tetrahydroimidazo[4,5-e][1,3]thiazolo[3,2-b][1,2,4]triazine-2,7(1H,6H)-diones”, Mendeleev Commun., 22:2 (2012), 90–91
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  • This publication is cited in the following 5 articles:
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