Review on Synthesis of (S)-5-Benzylpyrrolidine-2,4-dione Derivatives with Substitution at C-3 Position by Employing Functional Groups Interconversion
5-benzylpyrrolidine-2,4-dione 9 are versatile scaffolds with a unique structural feature responsible for the diversity of its biological importance. Over the past years, many researchers have reported the synthesis of various bio-active (S)-5-benzylpyrrolidine-2,4-dione derivatives due to their simp...
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2-s2.0-85132267308 Zulkifli M.; Pungot N.H.; Abdullah N.; Ash’ari N.A.N.; Shaameri Z. Review on Synthesis of (S)-5-Benzylpyrrolidine-2,4-dione Derivatives with Substitution at C-3 Position by Employing Functional Groups Interconversion 2022 Mini-Reviews in Organic Chemistry 19 6 10.2174/1570193X19666220110121158 https://www.scopus.com/inward/record.uri?eid=2-s2.0-85132267308&doi=10.2174%2f1570193X19666220110121158&partnerID=40&md5=7effce52750d4691c4d5ef27cc163945 5-benzylpyrrolidine-2,4-dione 9 are versatile scaffolds with a unique structural feature responsible for the diversity of its biological importance. Over the past years, many researchers have reported the synthesis of various bio-active (S)-5-benzylpyrrolidine-2,4-dione derivatives due to their simplicity yet exhibiting promising bioactivities. This review focuses on the synthesis of core structure 9 and its derivatives based on the substitution at carbon-3 position of (S)-5-benzylpyrrolidine2,4-dione 9. This review also reported the effective method for the synthesis of core structure 9 with a 98% yield. Biological evaluations of various prepared derivatives by various researchers were described. © 2022 Bentham Science Publishers. Bentham Science Publishers 1570193X English Article |
author |
Zulkifli M.; Pungot N.H.; Abdullah N.; Ash’ari N.A.N.; Shaameri Z. |
spellingShingle |
Zulkifli M.; Pungot N.H.; Abdullah N.; Ash’ari N.A.N.; Shaameri Z. Review on Synthesis of (S)-5-Benzylpyrrolidine-2,4-dione Derivatives with Substitution at C-3 Position by Employing Functional Groups Interconversion |
author_facet |
Zulkifli M.; Pungot N.H.; Abdullah N.; Ash’ari N.A.N.; Shaameri Z. |
author_sort |
Zulkifli M.; Pungot N.H.; Abdullah N.; Ash’ari N.A.N.; Shaameri Z. |
title |
Review on Synthesis of (S)-5-Benzylpyrrolidine-2,4-dione Derivatives with Substitution at C-3 Position by Employing Functional Groups Interconversion |
title_short |
Review on Synthesis of (S)-5-Benzylpyrrolidine-2,4-dione Derivatives with Substitution at C-3 Position by Employing Functional Groups Interconversion |
title_full |
Review on Synthesis of (S)-5-Benzylpyrrolidine-2,4-dione Derivatives with Substitution at C-3 Position by Employing Functional Groups Interconversion |
title_fullStr |
Review on Synthesis of (S)-5-Benzylpyrrolidine-2,4-dione Derivatives with Substitution at C-3 Position by Employing Functional Groups Interconversion |
title_full_unstemmed |
Review on Synthesis of (S)-5-Benzylpyrrolidine-2,4-dione Derivatives with Substitution at C-3 Position by Employing Functional Groups Interconversion |
title_sort |
Review on Synthesis of (S)-5-Benzylpyrrolidine-2,4-dione Derivatives with Substitution at C-3 Position by Employing Functional Groups Interconversion |
publishDate |
2022 |
container_title |
Mini-Reviews in Organic Chemistry |
container_volume |
19 |
container_issue |
6 |
doi_str_mv |
10.2174/1570193X19666220110121158 |
url |
https://www.scopus.com/inward/record.uri?eid=2-s2.0-85132267308&doi=10.2174%2f1570193X19666220110121158&partnerID=40&md5=7effce52750d4691c4d5ef27cc163945 |
description |
5-benzylpyrrolidine-2,4-dione 9 are versatile scaffolds with a unique structural feature responsible for the diversity of its biological importance. Over the past years, many researchers have reported the synthesis of various bio-active (S)-5-benzylpyrrolidine-2,4-dione derivatives due to their simplicity yet exhibiting promising bioactivities. This review focuses on the synthesis of core structure 9 and its derivatives based on the substitution at carbon-3 position of (S)-5-benzylpyrrolidine2,4-dione 9. This review also reported the effective method for the synthesis of core structure 9 with a 98% yield. Biological evaluations of various prepared derivatives by various researchers were described. © 2022 Bentham Science Publishers. |
publisher |
Bentham Science Publishers |
issn |
1570193X |
language |
English |
format |
Article |
accesstype |
|
record_format |
scopus |
collection |
Scopus |
_version_ |
1809677891358687232 |