The Journal of Organic Chemistry, Journal Year: 2024, Volume and Issue: 89(22), P. 16564 - 16570
Published: Oct. 31, 2024
An efficient method for phosphine-catalyzed sulfophosphinoylation of α,β-unsaturated ketones synthesis allylic organophosphorus compounds has been reported, in which acting as zwitterions react with electrophiles and nucleophiles to form a C-P bond C-O obtain high regio- stereoselectivity moderate excellent yields.
Language: Английский
ACS Catalysis, Journal Year: 2024, Volume and Issue: 14(4), P. 2395 - 2401
Published: Jan. 31, 2024
Functionalized sulfides are important in many areas of science, ranging from chemical biology through drug discovery to organic materials chemistry. Sulfides bearing pendant reactive groups the α-position particularly useful; however, methods for selective valorization simple or late-stage functionalization complex by convenient addition valuable functionality underexplored. Here we exemplify a general reaction platform sulfide showcasing three modes α-sulfur C-H functionalization; cyanation, alkenylation, and alkynylation. Using inexpensive commercially available riboflavin tetraacetate visible light, decoration both feedstock proceeds good yield with high selectivity. Methionine-containing peptides can also be selectively functionalized tolerance screen using amino-acid dopants suggests that is compatible most side chains thus potential tool bioconjugation.
Language: Английский
Citations
9
Organic Chemistry Frontiers, Journal Year: 2023, Volume and Issue: 10(19), P. 4972 - 5027
Published: Jan. 1, 2023
This review comprehensively summarizes the dichalcogenative functionalization of unsaturated compounds over past decade. The scopes, limitations and detailed reaction mechanisms are also discussed.
Language: Английский
Citations
20
Molecules, Journal Year: 2022, Volume and Issue: 27(19), P. 6583 - 6583
Published: Oct. 4, 2022
The significant scaffold offered by atropisomeric amides with a C–N chiral axis has been extensively utilized for pharmaceuticals, agricultural science, and organic syntheses. As result, the field of atropisomer synthesis attracted considerable interest within chemistry communities. To date, range catalytic atroposelective approaches reported efficient construction these challenging scaffolds. However, greatly concise highly useful methodologies compounds, focusing on transition-metal, amine, phosphoric acid catalysis reactions, etc., are still desirable. Hence, it is indispensable to succinctly systematically present all such reports means disclosing mechanistic analysis application, as well challenges issues associated establishment atropisomers. In this review, we summarize development asymmetric synthetic strategies access non-biaryl atropisomers rotating around axis, including reaction methods, mechanism, late-stage transformations, applications.
Language: Английский
Citations
23
Chinese Journal of Chemistry, Journal Year: 2024, Volume and Issue: 42(17), P. 2049 - 2055
Published: May 7, 2024
Comprehensive Summary An electrocatalytic multicomponent cascade cross‐coupling for the synthesis of chalcogenosulfonates has been established. This approach does not require use transition metals, acids, and external oxidants. The gentle conditions tolerance to a wide variety functional groups permit derivatization complex indoles.
Language: Английский
Citations
5
Organic Letters, Journal Year: 2023, Volume and Issue: 25(16), P. 2846 - 2851
Published: April 14, 2023
A photocatalyzed coupling-cyclization of sila-enynes with thiosulfonates has been developed. This reaction provides an efficient strategy to assemble thiosulfone-bifunctionalized benzosilacycles via sequential radical addition and coupling.
Language: Английский
Citations
13
Organic Letters, Journal Year: 2023, Volume and Issue: 25(39), P. 7078 - 7082
Published: Sept. 21, 2023
A metal-free oxidative trideuteromethylthiolation of alkenes with CD3SSO3Na using NFSI as an oxidant has been developed. The aminotrideuteromethylthiolation a three-component reaction could be easily achieved in the presence cobalt catalyst. divergent alkenes, readily available reagent, and versatile synthetic strategy allow for late-stage modification drug molecules.
Language: Английский
Citations
11
Organic Letters, Journal Year: 2022, Volume and Issue: 24(37), P. 6794 - 6799
Published: Sept. 14, 2022
A family of electrophilic deuterated methylthiolating reagents, S-(methyl-d3) arylsulfonothioates, was developed in two or three steps from cheap d4-MeOH high yields. S-(Methyl-d3) arylsulfonothioates represent a kind powerful reagent and allow modular trideuteromethylthiolation with variety nucleophiles electrophiles including aryl(hetero) iodides, boronic acids esters, terminal alkynes, diazonium salts, β-ketoester, oxindole under mild reaction conditions. structure–reactivity research (SAR) study conducted provided new avenue for the development reagents efficient methodology trideuteromethylthiolation.
Language: Английский
Citations
19
The Journal of Organic Chemistry, Journal Year: 2025, Volume and Issue: unknown
Published: April 22, 2025
The combination of sulfoxides with MOMCl has been found for the first time to mediate electrophilic cyclization and install a variety sulfenyl groups onto isocoumarin skeletons via regioselective cleavage reconfiguration C-S bonds. Notably, MOMCl, mild readily available alkyl chloride, was indispensable played significant role as an activator under neutral conditions in this transformation, thus expanding scope acid-labile substrates.
Language: Английский
Citations
0
Organic Letters, Journal Year: 2024, Volume and Issue: 26(27), P. 5705 - 5712
Published: June 27, 2024
Selenosulfones, as pivotal pharmaceutical molecule frameworks, have become a research hotspot in modern organic synthesis due to their vital need for efficient preparation. Herein, we developed an iron-catalyzed four-component controllable radical tandem reaction of allenes involving cycloketone oxime esters, 1,4-diazabicyclo[2.2.2]octane bis(sulfur dioxide) adduct (DABSO), and diphenyl diselenides the complex selenosulfones. This is first case achieving 1,2-selenosulfonylation via process, wherein precise control rates polarity matching enhance high regioselective conversion. The conditions are ecofriendly mild with step-efficiency by forming two new C–S bonds one C–Se bond pot. Moreover, can be achieved replacing esters aryldiazonium tetrafluoroborates this system.
Language: Английский
Citations
3
Organic Chemistry Frontiers, Journal Year: 2024, Volume and Issue: 11(21), P. 6064 - 6068
Published: Jan. 1, 2024
Three-component amino- and carbotrideuteromethylthiolation of alkenes in water.
Language: Английский
Citations
3