Modern photo- and electrochemical approaches to aryl radical generation DOI Creative Commons

Krzysztof Grudzień,

Andrei Zlobin,

Jan Zadworny

et al.

Organic Chemistry Frontiers, Journal Year: 2024, Volume and Issue: 11(18), P. 5232 - 5277

Published: Jan. 1, 2024

This review describes recent advances in the generation of aryl radicals using light and electricity. Such modern techniques allow for efficient energy resource utilization, thus providing more sustainable radical arylation methods.

Language: Английский

Advances in covalent drug discovery DOI Open Access
Lydia Boike, Nathaniel J. Henning, Daniel K. Nomura

et al.

Nature Reviews Drug Discovery, Journal Year: 2022, Volume and Issue: 21(12), P. 881 - 898

Published: Aug. 25, 2022

Language: Английский

Citations

498

Recent progress in self-healing polymers and hydrogels based on reversible dynamic B–O bonds: boronic/boronate esters, borax, and benzoxaborole DOI Creative Commons

Seungwan Cho,

Sung Yeon Hwang, Dongyeop X. Oh

et al.

Journal of Materials Chemistry A, Journal Year: 2021, Volume and Issue: 9(26), P. 14630 - 14655

Published: Jan. 1, 2021

Reversible boronic ester-based polymers/hydrogels achieve cutting-edge biomedical applications including drug delivery, adhesion, bioimplants, healthcare monitoring by self-healing, injectability, biocompatibility, multi-responsiveness to stimuli.

Language: Английский

Citations

277

Fighting antibiotic resistance—strategies and (pre)clinical developments to find new antibacterials DOI Creative Commons
Sebastian Walesch, Joy Birkelbach, Gwenaëlle Jézéquel

et al.

EMBO Reports, Journal Year: 2022, Volume and Issue: 24(1)

Published: Dec. 19, 2022

Language: Английский

Citations

116

The Rise of Boron-Containing Compounds: Advancements in Synthesis, Medicinal Chemistry, and Emerging Pharmacology DOI
R. Justin Grams, Webster L. Santos, Ion Romulus Scorei

et al.

Chemical Reviews, Journal Year: 2024, Volume and Issue: 124(5), P. 2441 - 2511

Published: Feb. 21, 2024

Boron-containing compounds (BCC) have emerged as important pharmacophores. To date, five BCC drugs (including boronic acids and boroles) been approved by the FDA for treatment of cancer, infections, atopic dermatitis, while some natural are included in dietary supplements. Boron's Lewis acidity facilitates a mechanism action via formation reversible covalent bonds within active site target proteins. Boron has also employed development fluorophores, such BODIPY imaging, carboranes that potential neutron capture therapy agents well novel diagnostics therapy. The utility synthetic become multifaceted, breadth their applications continues to expand. This review covers many uses targets boron medicinal chemistry.

Language: Английский

Citations

101

The Boron Advantage: The Evolution and Diversification of Boron’s Applications in Medicinal Chemistry DOI Creative Commons
Katia Messner, Billy Vuong, Geoffrey K. Tranmer

et al.

Pharmaceuticals, Journal Year: 2022, Volume and Issue: 15(3), P. 264 - 264

Published: Feb. 22, 2022

In this review, the history of boron's early use in drugs, and boron functional groups medicinal chemistry applications are discussed. This includes diazaborines, boronic acids, benzoxaboroles, clusters, carboranes. Furthermore, critical developments from these highlighted along with recent developments, which exemplify potential prospects. Lastly, application form a prodrug, softdrug, as nanocarrier discussed to showcase emergence into new exciting fields. Overall, we emphasize evolution organoboron therapeutic agents privileged structures outline impact that has had on drug discovery development.

Language: Английский

Citations

91

An update on the discovery and development of reversible covalent inhibitors DOI Open Access

Faridoon Faridoon,

Raymond A. Ng, Guiping Zhang

et al.

Medicinal Chemistry Research, Journal Year: 2023, Volume and Issue: 32(6), P. 1039 - 1062

Published: April 29, 2023

Language: Английский

Citations

48

Emerging Building Blocks for Medicinal Chemistry: Recent Synthetic Advances DOI
Oleksandr O. Grygorenko, Dmitriy M. Volochnyuk, Bohdan V. Vashchenko

et al.

European Journal of Organic Chemistry, Journal Year: 2021, Volume and Issue: 2021(47), P. 6478 - 6510

Published: Sept. 8, 2021

Abstract Current medicinal chemistry relies heavily on the quality of building blocks, i. e. reagents used to introduce chemical diversity into target molecules. The last decade witnessed an emergence many novel (or well‐overlooked old) chemotypes for drug discovery, which is related adapting new synthetic methodologies, designing sp 3 ‐enriched bioisosteres, paying attention previously underrated even unwanted) structural motifs, or combination thereof. In this review with 532 references, a survey selected that emerged recently in provided, focus synthesis corresponding blocks. Thus, saturated (hetero)aliphatic boronates, sulfonyl fluorides, sulfinates, non‐classical benzene isosteres, bicyclic morpholine/piperidine/piperazine analogs, as well gem ‐difluorinated cycloalkanes (as example emerging fluorinated motifs) are discussed.

Language: Английский

Citations

96

FDA-Approved Drugs for Hematological Malignancies—The Last Decade Review DOI Open Access
Aleksandra Sochacka-Ćwikła, Marcin Mą̨czyński, Andrzej Regiec

et al.

Cancers, Journal Year: 2021, Volume and Issue: 14(1), P. 87 - 87

Published: Dec. 24, 2021

Hematological malignancies, also referred to as blood cancers, are a group of diseases involving abnormal cell growth and persisting in the blood, lymph nodes, or bone marrow. The development new targeted therapies including small molecule inhibitors, monoclonal antibodies, bispecific T engagers, antibody-drug conjugates, recombinant immunotoxins, and, finally, Chimeric Antigen Receptor (CAR-T) cells has improved clinical outcomes for cancers. In this review, we summarized 52 drugs that were divided into macromolecule agents, approved by Food Drug Administration (FDA) period between 2011 2021 treatment hematological malignancies. Forty them have been European Medicines Agency (EMA). We analyzed FDA-approved investigating both their structures mechanisms action. It should be emphasized number was significantly higher (46 drugs) than chemotherapy agents (6 drugs). highlight recent advances design used treat which make more effective less toxic.

Language: Английский

Citations

71

Saturated Boronic Acids, Boronates, and Trifluoroborates: An Update on Their Synthetic and Medicinal Chemistry DOI
Dmitriy M. Volochnyuk, Alina O. Gorlova, Oleksandr O. Grygorenko

et al.

Chemistry - A European Journal, Journal Year: 2021, Volume and Issue: 27(62), P. 15277 - 15326

Published: Sept. 9, 2021

Abstract This review discusses recent advances in the chemistry of saturated boronic acids, boronates, and trifluoroborates. Applications title compounds design boron‐containing drugs are surveyed, with special emphasis on α‐amino derivatives. A general overview as modern tools to construct C(sp 3 )−C )‐heteroatom bonds is given, including developments Suzuki‐Miyaura Chan‐Lam cross‐couplings, single‐electron‐transfer processes metallo‐ organocatalytic photoredox reactions, transformations boron “ate” complexes. Finally, an attempt summarize current state art synthesis trifluoroborates made, a brief mention “classical” methods (transmetallation organolithium/magnesium reagents species, anti‐Markovnikov hydroboration alkenes, modification alkenyl compounds) focus methodologies (boronation alkyl (pseudo)halides, derivatives carboxylic alcohols, primary amines, boronative C−H activation, novel approaches alkene hydroboration, 1,2‐metallate‐type rearrangements).

Language: Английский

Citations

65

Electrochemical borylation of carboxylic acids DOI Open Access
Lisa M. Barton, Longrui Chen, Donna G. Blackmond

et al.

Proceedings of the National Academy of Sciences, Journal Year: 2021, Volume and Issue: 118(34)

Published: Aug. 17, 2021

Significance Boronic acids are one of the most useful functional groups in organic chemistry and can be used as intermediates synthesis or key motifs medicines. This work describes an extremely simple economical way to use electrochemistry convert carboxylic acids, through intermediacy redox-active esters, boronic acids. The scope this reaction is broad, mechanism has been thoroughly studied, it easily scaled up. Finally, application a complex polycyclopropane natural product demonstrated.

Language: Английский

Citations

63