Overlooked aza-S(iv) motifs: synthesis and transformations of sulfinamidines and sulfinimidate esters
Author:
Affiliation:
1. FLAME-Lab, Flow Chemistry and Microreactor Technology Laboratory Department of Pharmacy–Drug Sciences University of Bari “A. Moro” Via E., Orabona 4-70125 Bari, Italy
Abstract
Funder
Universita degli Studi di Bari Aldo Moro
Publisher
Royal Society of Chemistry (RSC)
Subject
Organic Chemistry,Physical and Theoretical Chemistry,Biochemistry
Link
http://pubs.rsc.org/en/content/articlepdf/2023/OB/D3OB01382K
Reference40 articles.
1. Analysis of US FDA-Approved Drugs Containing Sulfur Atoms
2. How do we address neglected sulfur pharmacophores in drug discovery?
3. Neglected sulfur(vi) pharmacophores in drug discovery: exploration of novel chemical space by the interplay of drug design and method development
4. Sulfoximines from a Medicinal Chemist's Perspective: Physicochemical and in vitro Parameters Relevant for Drug Discovery
5. Conversion and degradation pathways of sulfoximines
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1. Synthesis of chiral sulfilimines by organocatalytic enantioselective sulfur alkylation of sulfenamides;Science Advances;2024-09-13
2. Enantioselective Synthesis of Sulfinamidines via Asymmetric Nitrogen Transfer from N−H Oxaziridines to Sulfenamides;Angewandte Chemie International Edition;2024-06-21
3. Enantioselective Synthesis of Sulfinamidines via Asymmetric Nitrogen Transfer from N−H Oxaziridines to Sulfenamides;Angewandte Chemie;2024-06-21
4. N,N’‐Diaryl‐Sulfurdiimides are Strongly Redox Tuned;Chemistry – A European Journal;2024-03-22
5. Modular construction of sulfinimidate esters: expanding chemical space and enabling late-stage diversification;Organic Chemistry Frontiers;2024
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