N‐Chlorosulfonyloxazolidin‐2‐ones: Synthesis, Structure, and Reactivity Toward Aminoesters-Reference-Cited by-同舟云学术

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N‐Chlorosulfonyloxazolidin‐2‐ones: Synthesis, Structure, and Reactivity Toward Aminoesters

Published:2004-12-31 Issue:9 Volume:34 Page:1653-1662
ISSN:0039-7911
Container-title:Synthetic Communications
language:en
Short-container-title:Synthetic Communications

Author:

Berredjem Malika¹,Winum Jean‐Yves²,Toupet Loic³,Masmoudi Ouafae²,Aouf Nour‐Eddine¹,Montero Jean‐Louis²

Affiliation:

1. a Laboratoire de Chimie Bioorganique , Université d'Annaba , Annaba, Algérie

2. b Laboratoire de Chimie Biomoléculaire, UMR 5032 , Université Montpellier II, ENSCM , 8 rue de l'Ecole Normale, 34296, Montpellier, Cedex, France

3. c Groupe Matière Condensée et Matériaux, UMR 6626 , Université de Rennes I , Rennes, France

Publisher

Informa UK Limited

Subject

Organic Chemistry

Link

https://www.tandfonline.com/doi/pdf/10.1081/SCC-120030753

Reference28 articles.

1. 1,2-Amino Alcohols and Their Heterocyclic Derivatives as Chiral Auxiliaries in Asymmetric Synthesis

2. Enantioselective aldol condensations. 2. Erythro-selective chiral aldol condensations via boron enolates

3. Transition Stateπ-Solvation by Aromatic Rings: An Electronic Contribution to Diels–Alder Reaction Diastereoselectivity

4. Acyclic stereoselection. 54. Extending the scope of the Evans asymmetric aldol reaction: preparation of anti and "non-Evans" syn aldols

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2. Novel N-acylsulfamoyl-oxazolidin-2ones: Synthesis, antitumor activity, X-ray crystallographic study, molecular docking and POM analyses;Journal of Molecular Structure;2022-08

3. Synthesis, in silico study (DFT, ADMET) and crystal structure of novel sulfamoyloxy-oxazolidinones: Interaction with SARS-CoV-2;Journal of Molecular Structure;2022-06

4. A Novel and Green Method for N-acylation of Amines and Sulfonamides under Ultrasound Irradiation;Oriental Journal of Chemistry;2017-06-25

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