Batch and Continuous‐Flow Iron(II)‐Catalyzed Synthesis of Sulfilimines and Sulfoximines using N ‐Mesyloxycarbamates-Reference-Cited by-同舟云学术

Batch and Continuous‐Flow Iron(II)‐Catalyzed Synthesis of Sulfilimines and Sulfoximines using N ‐Mesyloxycarbamates

Published:2019-05-09 Issue:40 Volume:25 Page:9423-9426
ISSN:0947-6539
Container-title:Chemistry – A European Journal
language:en
Short-container-title:Chem. Eur. J.

Author:

Lai Calvine¹,Mathieu Gary¹,Gabrielli Tabarez Lucia Paola¹,Lebel Hélène¹^ORCID

Affiliation:

1. Department of Chemistry and Centre in Green Chemistry and Catalysis (CGCC)Université de Montréal P.O. Box 6128, Station Downtown Montréal QC H3C 3J7 Canada

Funder

Natural Sciences and Engineering Research Council of Canada

Fonds de Recherche du Québec - Nature et Technologies

Publisher

Wiley

Subject

General Chemistry,Catalysis,Organic Chemistry

Link

https://onlinelibrary.wiley.com/doi/pdf/10.1002/chem.201900953

Reference69 articles.

2. A Sulfilimine Bond Identified in Collagen IV

3. Sulfoximines: A Neglected Opportunity in Medicinal Chemistry

4. Sulfoximine: Eine vernachlässigte Chance in der medizinischen Chemie

5. Novel phthalamides containing sulfiliminyl moieties and derivatives as potential ryanodine receptor modulators

Cited by 20 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. Syntheses of Sulfilimines by Iron-Catalyzed Iminations of Sulfides with 2,2,2-Trichloroethyl Sulfamate;The Journal of Organic Chemistry;2024-06-13

2. Ligand‐Promoted Iron‐Catalyzed Nitrene Transfer for the Synthesis of Hydrazines and Triazanes through N‐Amidation of Arylamines;Angewandte Chemie International Edition;2023-12-06

3. Ligand‐Promoted Iron‐Catalyzed Nitrene Transfer for the Synthesis of Hydrazines and Triazanes through N‐Amidation of Arylamines;Angewandte Chemie;2023-12-06

4. A Domino Radical Amidation/Semipinacol Approach to All‐Carbon Quaternary Centers Bearing an Aminomethyl Group;Chemistry – A European Journal;2023-07-24

5. Sulfur-Arylation of Sulfenamides via Ullmann-Type Coupling with (Hetero)aryl Iodides;Organic Letters;2023-06-20