Spiro-condensation of 5-methoxycarbonyl-1H-pyrrole-2,3-diones with cyclic enoles to form spiro substituted furo[3,2-c]-coumarins and quinolines-Reference-Cited by-同舟云学术

Spiro-condensation of 5-methoxycarbonyl-1H-pyrrole-2,3-diones with cyclic enoles to form spiro substituted furo[3,2-c]-coumarins and quinolines

Published:2016 Issue:88 Volume:6 Page:84730-84737
ISSN:2046-2069
Container-title:RSC Advances
language:en
Short-container-title:RSC Adv.

Author:

Dubovtsev Alexey Yu.¹²³⁴,Silaichev Pavel S.¹²³⁴,Nazarov Mikhail A.¹²³⁴,Dmitriev Maksim V.¹²³⁴,Maslivets Andrey N.¹²³⁴,Rubin Michael¹⁵⁶⁷¹^ORCID

Affiliation:

1. Department of Chemistry

2. Perm State University

3. Perm 614990

4. Russia

5. North Caucasus Federal University

6. Stavropol 355009

7. Russian Federation

Abstract

Highly efficient spiro-cyclization enabling cyclic enoles to act as 1,3-bis-nucleophiles in reaction with pyrrole-2,3-diones acting as 1,2-bis-electrophiles was developed.

Funder

Ministry of Education and Science of the Russian Federation

Publisher

Royal Society of Chemistry (RSC)

Subject

General Chemical Engineering,General Chemistry

Link

http://pubs.rsc.org/en/content/articlepdf/2016/RA/C6RA16889B

Reference44 articles.

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3. Influence of storage conditions in the evolution of phytochemicals in nutraceutical products applying high resolution mass spectrometry

4. Enantiomeric 3-arylcoumarins and 2-arylcoumarones from the roots of Glycyrrhiza uralensis as protein tyrosine phosphatase 1B (PTP1B) inhibitors

5. Bioactive Constituents of Glycyrrhiza uralensis (Licorice): Discovery of the Effective Components of a Traditional Herbal Medicine

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