Efficient Synthesis of Pyrrolo[1,2-f]phenanthridine Derivatives via Dipolar Cycloaddition of Phenanthridine, Activated Acetylenes, and Ethyl Bromopyruvate
The three-component reactions of phenanthridine, activated acetylenes, and ethyl bromopyruvate through both of simultaneous and stepwise process are surveyed. The reactions afforded the corresponding pyrrolo[1,2-f]phenanthridine derivatives in good yields without using any catalyst and activation. [...
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Published in | Synthetic communications Vol. 44; no. 1; pp. 76 - 81 |
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Main Authors | , |
Format | Journal Article |
Language | English |
Published |
PHILADELPHIA
Taylor & Francis Group
02.01.2014
Taylor & Francis Taylor & Francis Ltd |
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ISSN | 0039-7911 1532-2432 |
DOI | 10.1080/00397911.2013.789525 |
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Abstract | The three-component reactions of phenanthridine, activated acetylenes, and ethyl bromopyruvate through both of simultaneous and stepwise process are surveyed. The reactions afforded the corresponding pyrrolo[1,2-f]phenanthridine derivatives in good yields without using any catalyst and activation.
[Supplementary materials are available for this article. Go to the publisher's online edition of Synthetic Communications® for the following free supplemental resource(s): Full experimental and spectral details.] |
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AbstractList | The three-component reactions of phenanthridine, activated acetylenes, and ethyl bromopyruvate through both of simultaneous and stepwise process are surveyed. The reactions afforded the corresponding pyrrolo[1,2-f]phenanthridine derivatives in good yields without using any catalyst and activation. [Supplementary materials are available for this article. Go to the publisher's online edition of Synthetic Communications (R) for the following free supplemental resource(s): Full experimental and spectral details.] The three-component reactions of phenanthridine, activated acetylenes, and ethyl bromopyruvate through both of simultaneous and stepwise process are surveyed. The reactions afforded the corresponding pyrrolo[1,2-f]phenanthridine derivatives in good yields without using any catalyst and activation. [Supplementary materials are available for this article. Go to the publisher's online edition of Synthetic Communications® for the following free supplemental resource(s): Full experimental and spectral details.] The three-component reactions of phenanthridine, activated acetylenes, and ethyl bromopyruvate through both of simultaneous and stepwise process are surveyed. The reactions afforded the corresponding pyrrolo[1,2-f]phenanthridine derivatives in good yields without using any catalyst and activation. [Supplementary materials are available for this article. Go to the publisher's online edition of Synthetic Communications® for the following free supplemental resource(s): Full experimental and spectral details.] [PUBLICATION ABSTRACT] |
Author | Mehrabi, Hossein Pishahang, Jaleh |
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Keywords | three-component reactions 2-f]phenanthridines ANALOGS AZOMETHINE YLIDES pyrrolo AGENTS Ethyl bromopyruvate phenanthridine DIMETHYL ACETYLENEDICARBOXYLATE |
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SubjectTerms | Chemistry Chemistry, Organic Ethyl bromopyruvate phenanthridine Physical Sciences pyrrolo[1,2-f]phenanthridines Science & Technology three-component reactions |
Title | Efficient Synthesis of Pyrrolo[1,2-f]phenanthridine Derivatives via Dipolar Cycloaddition of Phenanthridine, Activated Acetylenes, and Ethyl Bromopyruvate |
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