Rearrangement of unsym-azetidinone disulphides to 2β-(thio-substituted methyl) penams
Author:
Publisher
Elsevier BV
Subject
Organic Chemistry,Drug Discovery,Biochemistry
Reference17 articles.
1. Studies on β-lactam antibiotics. I. A novel conversion of penicillins into cephalosporins
2. Desulphurative approaches to penem antibiotics. II. 4-acyldithioazetidin-2-ones from penicillin derived sulphenimides, thiolsulphonates and disulphides.
3. Desulphurative approaches to penem antibiotics. V. 2-(Functionalized methyl)penems from 3-methylenecepham-1-oxides
4. Desulphurative approaches to penem antibiotics. VI. From penam methyl esters to penem acetonyl esters: A fully conservative conversion
5. Synthesis and .BETA.-lactamase inhibitory properties of 2.BETA.-(thio-substituted methyl)-penam 1,1-dioxides.
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1. Synthesis of Dihydrobenzoxazine‐Fused Spirooxazoline‐4‐ones via [3+2] Cycloaddition of Azaoxyallyl Cations with Vinyl Benzoxazinanones;Asian Journal of Organic Chemistry;2019-10-14
2. [3 + 2] Cycloaddition of Azaoxyallyl Cations with Cyclic Ketones: Access to Spiro-4-oxazolidinones;The Journal of Organic Chemistry;2017-09-26
3. ChemInform Abstract: Rearrangement of unsym-Azetidinone Disulfides to 2β-(Thio- Substituted-Methyl)penams.;ChemInform;2010-08-23
4. A Versatile Strategy for the Solid-Phase Synthesis of Penicillin Derivatives: Efficient Preparation of 2β-Methyl Substituted Penams as β-Lactamase Inhibitor Analogues;Synthesis;2006-10
5. Activation of Leinamycin by Thiols: A Theoretical Study;The Journal of Organic Chemistry;2002-11-13
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