4.2.3.3. Knorr Synthesis of Diethyl 3,5-Dimethyl-1<i>H</i>-pyrrole-2,4-dicarboxylate-Reference-Cited by-同舟云学术

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4.2.3.3. Knorr Synthesis of Diethyl 3,5-Dimethyl-1H-pyrrole-2,4-dicarboxylate

Published:2016-12-16 Issue: Volume: Page:373-375
ISSN:
Container-title:Comprehensive Organic Chemistry Experiments for the Laboratory Classroom
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Author:

Pino-González M. Soledad¹,García-Ruiz Cristina¹,Sarabia Francisco¹,Torres Gregorio¹

Affiliation:

1. Organic Chemistry Department, Faculty of Sciences, University of Málaga 29071 Málaga Spain pino@uma.es

Publisher

The Royal Society of Chemistry

Link

https://books.rsc.org/books/edited-volume/chapter-pdf/1686448/bk9781849739634-00373.pdf

Reference11 articles.

1. RECENT ADVANCES IN THE SYNTHESIS OF PYRROLES

2. The Absolute Configuration of Axinellamine A, a Pyrrole Alkaloid of the Marine SpongeAxinella sp., was Determined asR by Synthesizing Its (S)-Isomer

3. Synthesis and antimicrobial activity of new bromine-rich pyrrole derivatives related to monodeoxypyoluteorin

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