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 …
field of organic synthesis. Rhodium complexes are widely used as catalysts in a variety of …
Sulfonamide derivatives as multi-target agents for complex diseases
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 …
a century after Gerhard Domagk's pioneering work leading to the first sulfonamide antibiotic …
Sulfoximines as rising stars in modern drug discovery? Current status and perspective on an emerging functional group in medicinal chemistry
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 …
However, recently, they have risen to the apparent level of stardom on the drug discovery …
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 …
chemistry, yet methods for the synthesis of alkyl variants that start from simple, readily …
Data science-enabled palladium-catalyzed enantioselective aryl-carbonylation of sulfonimidamides
New methods for the general asymmetric synthesis of sulfonimidamides are of great interest
due to their applications in medicinal chemistry, agrochemical discovery, and academic …
due to their applications in medicinal chemistry, agrochemical discovery, and academic …
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 …
pharmacophores in drug discovery even though they offer very interesting properties. This …
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 …
an important role in asymmetric synthesis as versatile auxiliaries, ligands, and catalysts …
Synthesis of chiral sulfinate esters by asymmetric condensation
Achiral sulfur functional groups, such as sulfonamide, sulfone, thiol and thioether, are
common in drugs and natural products. By contrast, chiral sulfur functional groups are often …
common in drugs and natural products. By contrast, chiral sulfur functional groups are often …
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 …
significant attention recently due to their increasing use as pharmacophores in drug …
New Opportunities for the Utilization of the Sulfoximine Group in Medicinal Chemistry from the Drug Designer's Perspective
U Lücking - Chemistry–A European Journal, 2022 - Wiley Online Library
Extension of the medicinal chemistry toolbox is in the vital interest of drug designers.
However, the diffusion of an innovation can be a lengthy process. Along these lines, it took …
However, the diffusion of an innovation can be a lengthy process. Along these lines, it took …