Stereoselective synthesis and Lewis acid mediated functionalization of novel 3-methylthio-β-lactams
Author:
Publisher
Elsevier BV
Subject
Organic Chemistry,Drug Discovery,Biochemistry
Reference32 articles.
1. Selective Bond Cleavage of the β-Lactam Nucleus: Application in Stereocontrolled Synthesis
2. β-Lactams as Versatile Intermediates in α- and β-Amino Acid Synthesis
3. 4-Oxoazetidine-2-carbaldehydes as useful building blocks in stereocontrolled synthesis
4. From?-lactams to?- and?-amino acid derived peptides
5. Asymmetric synthesis of building-blocks for peptides and peptidomimetics by means of the β-lactam synthon method
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1. A highly stereoselective oxidation and an easy one pot elimination methodology for 3-allyl-3-phenylthio-β-lactams;Journal of Sulfur Chemistry;2021-12-14
2. Studies towards synthesis and Lewis acid catalysed functionalization of 3-(4′-substitutedphenylthio)-azetidin-2-ones;Journal of Chemical Sciences;2020-09-23
3. Stereoselective synthesis of trans-3-functionalized-4-pyrazolo[5,1-b]thiazole-3-carboxylate substituted β-lactams: Potential synthons for diverse biologically active agents;Synthetic Communications;2020-07-09
4. Stereoselective C-3 alkylation of trans-3-phenylsulfonyl-β-lactams with organic halides to access C-3 substituted β-lactams using sulfonyl moiety as an activating group;Tetrahedron Letters;2020-07
5. A Facile and Stereoselective Synthesis of 3‐Phenylsulfinyl‐β‐lactams Using Selectfluor;ChemistrySelect;2019-12-18
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