Results 201 to 210 of about 86,041 (331)

QM/MM Free Energy Calculations of IRE1 Reveal a Unique Protonation State of the Catalytic Lys599. [PDF]

J Comput Chem
Carlesso A, Conflitti P, Mahdizadeh SJ, Deganutti G, Eriksson LA, Limongelli V.   +5 more
europepmc   +1 more source

Nutzung des kooperativen Energie‐ und Wasserstofftransfers für die direkte Aminierung von nicht aktivierten Alkanen

Angewandte Chemie, Volume 138, Issue 3, 16 January 2026.
Kooperativer EnT & HAT: neue Methode zur direkten C─N‐Kopplung von nicht aktivierten Alkanen. Metallfreie photokatalytische Aminierung. Verwendung von nicht aktivierten Alkanen. Neuartiger Reaktionsweg. Abstrakt Während in letzter Zeit wichtige Fortschritte bei der direkten Funktionalisierung von Alkanen durch photokatalytische Verfahren erzielt wurden,
Sai Teja Kolla, Àlex Díaz‐Jiménez, Sven Trienes, Ignacio Funes‐Ardoiz, Joanna Wencel‐Delord   +4 more
wiley   +1 more source

Camphor-10-Sulfonamide Amino Acid Esters: Synthesis, Antiviral Evaluation, and Molecular Docking Insights. [PDF]

Int J Mol Sci
Dikova K, Vilhelmova-Ilieva N, Mateev E, Petkova Z.   +3 more
europepmc   +1 more source

Electrooxidative Divergent Halocyclizations of Ambident Amides

Angewandte Chemie, Volume 138, Issue 2, 9 January 2026.
Electrooxidation enables tunable halocyclization of ambident amides, yielding either C–O or C–N products through ionic or radical pathways, respectively. While detailed experimental and analytical mechanistic studies highlight mode‐dependent selectivity, in silico experimentation provided insight into the energetic origin of this divergence.
Minki Jeon, Debajit Maiti, Geon Kang, Jinwoo Kim, Isaac Choi   +4 more
wiley   +2 more sources

Design, synthesis and SAR of novel naphthalene-sulfonamide hybrids: anticancer assessment, gene expression analysis of IL6/JAK2/STAT3 signaling in MCF7 cells and antimicrobial evaluation. [PDF]

RSC Adv
Elsayed GH, Abdelazeem NM, Saleh AM, Abd El-Moez S, El-Hussieny M, Al-Ashmawy AAK.   +5 more
europepmc   +1 more source

Enantioconvergent Access to Chiral S(VI) Stereocenters by Kinetic Resolution of Sulfonimidoyl Chlorides

Angewandte Chemie, Volume 138, Issue 2, 9 January 2026.
An enantioconvergent approach for the kinetic resolution of S(VI) stereocenters that leverages the electrophilic reactivity of the chiral sulfur atom is described. The catalytic process provides access to sulfonimidoyl chlorides and sulfonimidates, which are among the least studied S(VI) functionalities.
Arko Das, Shree Krishna Dhakal, Ramon Trevino, Seth O. Fremin, Vy T. B. Nguyen, Arka Porey, Sachchida Nand, Chandan Kumar Giri, Daniel J. Wherritt, Hadi D. Arman, Oleg V. Larionov   +10 more
wiley   +2 more sources

Recent advances in the synthesis of <i>N</i>-acyl sulfonamides. [PDF]

RSC Adv
O'Driscoll M, Reddy GS, O'Sullivan TP.
europepmc   +1 more source

X-ray crystallographic and kinetic studies of biguanide containing aryl sulfonamides as carbonic anhydrase inhibitors

Chiara Baroni, Murat Bozdağ, Gioele Renzi, Viviana De Luca, Clemente Capasso, Carla Bazzicalupi, Silvia Selleri, Marta Ferraroni, Fabrizio Carta, Claudiu T. Supuran   +9 more
openalex   +2 more sources

Fluoride‐Transfer Asymmetric Allylic Alkylation Enables Regiodivergent, Stereoselective Cross‐Electrophile Coupling

Angewandte Chemie, Volume 138, Issue 2, 9 January 2026.
We report a fluoride‐transfer asymmetric allylic alkylation (AAA) in which all reagent atoms, including the leaving group, are incorporated into the products. This atom‐efficient AAA protocol enables the cross‐electrophile coupling of allyl fluorides and gem‐difluoroalkenes, providing a catalyst‐controlled, regiodivergent, and stereoselective access to
Jordi Duran, Vyali Georgian Moldoveanu, Claudia Barroso, Geraldo Augusto Pereira, Bart Limburg, Xavier Companyó   +5 more
wiley   +2 more sources

Total Synthesis of the Cyanobacterial Alkaloid Nostodione A

European Journal of Organic Chemistry, Volume 29, Issue 2, January 16, 2026.
The total synthesis of the alkaloid nostodione A is successfully achieved utilizing 3,4‐dihydrocyclopenta[b]indole‐1,2‐dione as a key intermediate. The sensitive benzylidene moiety is introduced via a Knoevenagel condensation with p‐hydroxybenzaldehyde.
Oscar F. Casadiego‐Díaz, Ángel Rentería‐Gómez, Teresa Ramírez‐Apan, Rubén O. Torres‐Ochoa   +3 more
wiley   +1 more source