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Three‐Component One‐Pot Synthesis of Indolo[3,4‐ a ]acridine Derivatives with High Regioselectivity under Catalyst‐Free Conditions

Three‐component reaction of aldehyde, 9‐ethyl‐9‐carbazol‐3‐amine, and 5,5‐dimethyl cyclohexane‐1,3‐dione under catalyst‐free conditions in EtOH, regioselectivity gave corresponding indolo[3,4‐]acridine rather than indolo[2,3‐]acridine derivatives in high yields, which is confirmed by X‐ray diffracti... Full description

Journal Title: Journal of Heterocyclic Chemistry August 2014, Vol.51(S1), pp.E349-E353
Main Author: Zhang, Mei‐Mei
Other Authors: Wang, Wei , Wang, Xiang‐Shan
Format: Electronic Article Electronic Article
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ID: ISSN: 0022-152X ; E-ISSN: 1943-5193 ; DOI: 10.1002/jhet.1896
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recordid: wj10.1002/jhet.1896
title: Three‐Component One‐Pot Synthesis of Indolo[3,4‐ a ]acridine Derivatives with High Regioselectivity under Catalyst‐Free Conditions
format: Article
creator:
  • Zhang, Mei‐Mei
  • Wang, Wei
  • Wang, Xiang‐Shan
subjects:
  • Resveratrol
ispartof: Journal of Heterocyclic Chemistry, August 2014, Vol.51(S1), pp.E349-E353
description: Three‐component reaction of aldehyde, 9‐ethyl‐9‐carbazol‐3‐amine, and 5,5‐dimethyl cyclohexane‐1,3‐dione under catalyst‐free conditions in EtOH, regioselectivity gave corresponding indolo[3,4‐]acridine rather than indolo[2,3‐]acridine derivatives in high yields, which is confirmed by X‐ray diffraction analysis.
language:
source:
identifier: ISSN: 0022-152X ; E-ISSN: 1943-5193 ; DOI: 10.1002/jhet.1896
fulltext: fulltext
issn:
  • 0022-152X
  • 0022152X
  • 1943-5193
  • 19435193
url: Link


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descriptionThree‐component reaction of aldehyde, 9‐ethyl‐9‐carbazol‐3‐amine, and 5,5‐dimethyl cyclohexane‐1,3‐dione under catalyst‐free conditions in EtOH, regioselectivity gave corresponding indolo[3,4‐]acridine rather than indolo[2,3‐]acridine derivatives in high yields, which is confirmed by X‐ray diffraction analysis.
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titleThree‐Component One‐Pot Synthesis of Indolo[3,4‐ a ]acridine Derivatives with High Regioselectivity under Catalyst‐Free Conditions
descriptionThree‐component reaction of aldehyde, 9‐ethyl‐9‐carbazol‐3‐amine, and 5,5‐dimethyl cyclohexane‐1,3‐dione under catalyst‐free conditions in EtOH, regioselectivity gave corresponding indolo[3,4‐]acridine rather than indolo[2,3‐]acridine derivatives in high yields, which is confirmed by X‐ray diffraction analysis.
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authorZhang, Mei‐Mei ; Wang, Wei ; Wang, Xiang‐Shan
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abstractThree‐component reaction of aldehyde, 9‐ethyl‐9‐carbazol‐3‐amine, and 5,5‐dimethyl cyclohexane‐1,3‐dione under catalyst‐free conditions in EtOH, regioselectivity gave corresponding indolo[3,4‐]acridine rather than indolo[2,3‐]acridine derivatives in high yields, which is confirmed by X‐ray diffraction analysis.
doi10.1002/jhet.1896
pagesE349-E353
date2014-08