The reaction of electron excess aromatic heterocycle, 1,4-dihydropyrrolo[3,2-b]pyrrole and some related compounds with chlorosulfonyl isocyanate (CSI)

Kyosuke Satake; Kentaro Yano; Makoto Fujiwara; Masaiu Kimura

doi:10.3987/COM-96-7616

The reaction of electron excess aromatic heterocycle, 1,4-dihydropyrrolo[3,2-b]pyrrole and some related compounds with chlorosulfonyl isocyanate (CSI)

Kyosuke Satake, Kentaro Yano, Makoto Fujiwara, Masaiu Kimura

Institute for Education and Student Services

Research output: Contribution to journal › Article › peer-review

8 Citations (Scopus)

Abstract

The reaction of 3,6-di-tert-butyl-l,4-dihydropyrrolo[3,2-b]pyrrole and its N,N' -dimethoxycarbonyl derivative with chlorosulfonyl isocyanate (CSI) was investigated. The higher reactivity for the electrophilic reaction and a remarkable electron excessiveness of the system were demonstrated by comparing with those of indole and pyrrole derivatives.

Original language	English
Pages (from-to)	2361-2365
Number of pages	5
Journal	Heterocycles
Volume	43
Issue number	11
DOIs	https://doi.org/10.3987/COM-96-7616
Publication status	Published - Jan 1 1996

ASJC Scopus subject areas

Analytical Chemistry
Pharmacology
Organic Chemistry

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abstract = "The reaction of 3,6-di-tert-butyl-l,4-dihydropyrrolo[3,2-b]pyrrole and its N,N' -dimethoxycarbonyl derivative with chlorosulfonyl isocyanate (CSI) was investigated. The higher reactivity for the electrophilic reaction and a remarkable electron excessiveness of the system were demonstrated by comparing with those of indole and pyrrole derivatives.",

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AU - Satake, Kyosuke

AU - Yano, Kentaro

AU - Fujiwara, Makoto

AU - Kimura, Masaiu

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Y1 - 1996/1/1

N2 - The reaction of 3,6-di-tert-butyl-l,4-dihydropyrrolo[3,2-b]pyrrole and its N,N' -dimethoxycarbonyl derivative with chlorosulfonyl isocyanate (CSI) was investigated. The higher reactivity for the electrophilic reaction and a remarkable electron excessiveness of the system were demonstrated by comparing with those of indole and pyrrole derivatives.

AB - The reaction of 3,6-di-tert-butyl-l,4-dihydropyrrolo[3,2-b]pyrrole and its N,N' -dimethoxycarbonyl derivative with chlorosulfonyl isocyanate (CSI) was investigated. The higher reactivity for the electrophilic reaction and a remarkable electron excessiveness of the system were demonstrated by comparing with those of indole and pyrrole derivatives.

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The reaction of electron excess aromatic heterocycle, 1,4-dihydropyrrolo[3,2-b]pyrrole and some related compounds with chlorosulfonyl isocyanate (CSI)

Abstract

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