Alternative Approach to Access 5-Hydroxy-1H-pyrrol-2-(5H)-ones from Base-Induced Tandem Intramolecular Cyclization of Sulfur Ylide with Ketones and 1,3-Hydroxy Rearrangement-Reference-Cited by-同舟云学术

Alternative Approach to Access 5-Hydroxy-1H-pyrrol-2-(5H)-ones from Base-Induced Tandem Intramolecular Cyclization of Sulfur Ylide with Ketones and 1,3-Hydroxy Rearrangement

Published:2023-12-04 Issue:50 Volume:8 Page:48251-48257
ISSN:2470-1343
Container-title:ACS Omega
language:en
Short-container-title:ACS Omega

Author:

Preetham Habbanakuppe D.¹,Sharath Kumar Kothanahally S.¹,Kandaswamy Aravind²,Rangappa Shobith³,Gatasheh Mansour K.⁴,Muddegowda Umashankara⁵^ORCID,Rangappa Kanchugarakoppal S.¹

Affiliation:

1. Department of Studies in Chemistry, University of Mysore, Manasagangotri, Mysuru 570006. India

2. Graduate School of Life Science, Hokkaido University, Kita 21, Nishi 11, Sapporo 001-0021, Japan

3. Adichunchanagiri Institute for Molecular Medicine, Adichunchanagiri University, B. G. Nagar, Bellur 571448 ,India

4. Department of Biochemistry, College of Science, King Saud University, P.O.Box 2455, Riyadh 11451, Saudi Arabia

5. Department of Studies and Research in Chemistry, Karnataka State Open University, Mukthagangotri, Mysuru 570006, India

Funder

Council of Scientific and Industrial Research, India

University of Mysore

King Saud University

Publisher

American Chemical Society (ACS)

Subject

General Chemical Engineering,General Chemistry

Link

https://pubs.acs.org/doi/pdf/10.1021/acsomega.3c06866

Reference45 articles.

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4. Chemistry and biology of non-tetramic γ-hydroxy-γ-lactams and γ-alkylidene-γ-lactams from natural sources

5. Inhibition of Enterococcus faecalis biofilm formation by highly active lactones and lactams analogues of rubrolides

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