Facile synthesis of novel benzothiazolylpyrazolyl anchored 3-thio/seleno/chloro-β-lactams: Synthetic intermediates for novel 3-sulfenyl/sulfonyl, C-3 functionalized monocyclic and spirocyclic β-lactams
Author:
Affiliation:
1. Department of Chemistry, Dev Samaj College for Women, Chandigarh, India;
2. Department of Chemistry and Centre of Advanced Studies in Chemistry, Panjab University, Chandigarh, India
Funder
Department of Science and Technology (DST), New Delhi, Government of India
University Grants Commission (UGC), New Delhi, India
Publisher
Informa UK Limited
Subject
Organic Chemistry
Link
https://www.tandfonline.com/doi/pdf/10.1080/00397911.2018.1515366
Reference20 articles.
1. Chemical Synthesis of β-Lactams: Asymmetric Catalysis and Other Recent Advances
2. Asymmetric synthesis of building-blocks for peptides and peptidomimetics by means of the β-lactam synthon method
3. β-Lactams: Versatile Building Blocks for the Stereoselective Synthesis of Non-β-Lactam Products
4. A comprehensive review in current developments of benzothiazole-based molecules in medicinal chemistry
5. N-Thiolated β-lactams: A new family of anti-Bacillus agents
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1. Stereoselective synthesis of trans-benzo[d]oxazolyl)phenyl substituted β-lactams decorated with C-3 thio/seleno rich motifs: synthetic intermediates for diverse heterocycles;Journal of Sulfur Chemistry;2023-05-02
2. Stereoselective synthesis and in-silico evaluation of C4-benzimidazolyloxyphenyl substituted trans-β-lactam derivatives as promising novel PPARγ activators;Synthetic Communications;2021-10-19
3. Four-Membered Ring Systems;Progress in Heterocyclic Chemistry;2020
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