1,3-Dipolar Cycloadditions of Phenanthridinium-Based Azomethine Ylides

DOSTÁL, Jiří, Milan POTÁČEK, Otakar HUMPA and Jaromír MAREK. 1,3-Dipolar Cycloadditions of Phenanthridinium-Based Azomethine Ylides. Bulletin des Sociétés Chimiques Belges. Brusel: Société Royale de Chimie, 1994, vol. 103, 7-8, p. 343-348. ISSN 0037-9646.

Basic information

Original name

1,3-Dipolar Cycloadditions of Phenanthridinium-Based Azomethine Ylides

Name in Czech

1,3-Dipolar Cycloadditions of Phenanthridinium-Based Azomethine Ylides

Authors

DOSTÁL, Jiří (203 Czech Republic, guarantor), Milan POTÁČEK (203 Czech Republic), Otakar HUMPA (203 Czech Republic) and Jaromír MAREK (203 Czech Republic)

Edition

Bulletin des Sociétés Chimiques Belges, Brusel, Société Royale de Chimie, 1994, 0037-9646

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Other information

Language

English

Type of outcome

Článek v odborném periodiku

Field of Study

10401 Organic chemistry

Country of publisher

Belgium

Confidentiality degree

není předmětem státního či obchodního tajemství

Organization unit

Faculty of Science

UT WoS

A1994PQ31500006

Keywords (in Czech)

Dipolar Cycloadditions; Phenanthridinium; Azomethine Ylides

Keywords in English

Dipolar Cycloadditions; Phenanthridinium; Azomethine Ylides

Tags

Azomethine Ylides, Dipolar Cycloadditions, Phenanthridinium

Tags

International impact, Reviewed

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Abstract

V originále

1,3-Dipolar Cycloadditions; Phenanthridinium; Azomethine Ylides. Azomethine ylides generated from 5-(alkoxycarbonylmethyl)phenanthridinium cations were studied in 1,3-dipolar cycloadditions with dimethyl maleate and dimethyl fumarate as dipolarophiles. The cycloadducts with the pyrrolidino[1,2-f]phenanthridine skeleton easily underwent dehydrogenation. The structure of products was determined by X-ray, NMR and MS.

In Czech

1,3-Dipolar Cycloadditions; Phenanthridinium; Azomethine Ylides