Rhodium‐Catalyzed C(sp2)‐ or C(sp3)−H Bond Functionalization Assisted by Removable Directing Groups

S Rej, N Chatani - Angewandte Chemie International Edition, 2019 - Wiley Online Library
In recent years, transition‐metal‐catalyzed C− H activation has become a key strategy in the
field of organic synthesis. Rhodium complexes are widely used as catalysts in a variety of …

Modern stereoselective synthesis of chiral sulfinyl compounds

E Wojaczyńska, J Wojaczyński - Chemical reviews, 2020 - ACS Publications
Chiral sulfinyl compounds, sulfoxides, sulfoximines, sulfinamides, and other derivatives, play
an important role in asymmetric synthesis as versatile auxiliaries, ligands, and catalysts …

Sulfoximines as rising stars in modern drug discovery? Current status and perspective on an emerging functional group in medicinal chemistry

P Mäder, L Kattner - Journal of Medicinal Chemistry, 2020 - ACS Publications
Sulfoximines have been largely disregarded in medicinal chemistry for a long time.
However, recently, they have risen to the apparent level of stardom on the drug discovery …

Enantioselective construction of stereogenic-at-sulfur (IV) centres via catalytic acyl transfer sulfinylation

T Wei, HL Wang, Y Tian, MS **e, HM Guo - Nature Chemistry, 2024 - nature.com
Chiral sulfur pharmacophores are crucial for drug discovery in bioscience and medicinal
chemistry. While the catalytic asymmetric synthesis of sulfoxides and sulfinate esters with …

Photocatalytic carboxylate to sulfinamide switching delivers a divergent synthesis of sulfonamides and sulfonimidamides

JA Andrews, J Kalepu, CF Palmer… - Journal of the …, 2023 - ACS Publications
sulfinamides, sulfonamides, and sulfonimidamides are in-demand motifs in medicinal
chemistry, yet methods for the synthesis of alkyl variants that start from simple, readily …

Neglected sulfur (VI) pharmacophores in drug discovery: exploration of novel chemical space by the interplay of drug design and method development

U Lücking - Organic Chemistry Frontiers, 2019 - pubs.rsc.org
Historically, sulfoximines, sulfondiimines and sulfonimidamides have been neglected
pharmacophores in drug discovery even though they offer very interesting properties. This …

Data science-enabled palladium-catalyzed enantioselective aryl-carbonylation of sulfonimidamides

L van Dijk, BC Haas, NK Lim, K Clagg… - Journal of the …, 2023 - ACS Publications
New methods for the general asymmetric synthesis of sulfonimidamides are of great interest
due to their applications in medicinal chemistry, agrochemical discovery, and academic …

Asymmetric synthesis of S (IV) and S (VI) stereogenic centers

X Zhang, F Wang, CH Tan - JACS Au, 2023 - ACS Publications
Sulfur can form diverse S (IV) and S (VI) stereogenic centers, of which some have gained
significant attention recently due to their increasing use as pharmacophores in drug …

Asymmetric synthesis of sulfoximines, sulfonimidoyl fluorides and sulfonimidamides enabled by an enantiopure bifunctional S (VI) reagent

S Teng, ZP Shultz, C Shan, L Wojtas, JM Lopchuk - Nature chemistry, 2024 - nature.com
An increased interest to expand three-dimensional chemical space for the design of new
materials and medicines has created a demand for isosteric replacement groups of …

Sulfonamide derivatives as multi-target agents for complex diseases

S Apaydın, M Török - Bioorganic & medicinal chemistry letters, 2019 - Elsevier
Sulfonamide derivatives are frequently seen structural motifs in medicinal chemistry. Almost
a century after Gerhard Domagk's pioneering work leading to the first sulfonamide antibiotic …