Double 1,3‐dipolar  cycloaddition  of  N ‐methyl Azomethine ylide to meta‐Dinitrobenzene annelated with nitrogen aromatic heterocycles | Zendy

Bastrakov Maxim A. | Zendy; Starosotnikov Alexey M. | Zendy; Pechenkin Sergey Yu. | Zendy; Kachala Vadim V. | Zendy; Glukhov Ivan V. | Zendy; Shevelev Svyatoslav A. | Zendy

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Double 1,3‐dipolar cycloaddition of N ‐methyl Azomethine ylide to meta‐Dinitrobenzene annelated with nitrogen aromatic heterocycles

Author(s) -

Bastrakov Maxim A.,

Starosotnikov Alexey M.,

Pechenkin Sergey Yu.,

Kachala Vadim V.,

Glukhov Ivan V.,

Shevelev Svyatoslav A.

Publication year - 2010

Publication title -

journal of heterocyclic chemistry

Language(s) - English

Resource type - Journals

SCImago Journal Rank - 0.321

H-Index - 59

eISSN - 1943-5193

pISSN - 0022-152X

DOI - 10.1002/jhet.423

Subject(s) - azomethine ylide , chemistry , cycloaddition , isoindole , 1,3 dipolar cycloaddition , nitrogen , ylide , medicinal chemistry , organic chemistry , catalysis

The 1,3‐dipolar cycloaddition of unstabilized azomethine ylide 1 with meta‐dinitrobenzene fused with nitrogen heterocycles affords the corresponding decahydropyrrolo[3,4‐ e ]isoindole cycloadducts in good yields. This is a first example of [3+2]‐cycloaddition of azomethine ylides to nitroarenes. J. Heterocyclic Chem., (2010).

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