A catalyst-free cross-dehydrogenative coupling reaction of purines and some azoarenes with dialkyl disulfides has been developed. This procedure provided a novel strategy to construct unsymmetrical disulfides through the α-heterocyclic functionalization of symmetrical dialkyl disulfides. The S-S bond was successfully tolerated in this transformation. The mild conditions and the broad scope of azoarenes indicated the potential application of this procedure.
Download full-text PDF |
Source |
---|---|
http://dx.doi.org/10.1021/acs.joc.0c00953 | DOI Listing |
J Org Chem
December 2024
School of Chemistry and Materials Science, Jiangsu Provincial Key Laboratory of Material Cycle Processes and Pollution Control, Jiangsu Collaborative Innovation Center of Biomedical Functional Materials, Nanjing Normal University, Nanjing 210023, China.
Inorg Chem
November 2024
Key Laboratory of Applied Chemistry of Chongqing Municipality, College of Chemistry and Chemical Engineering, Southwest University, Chongqing 400715, China.
Cerium and lanthanum dialkyl complexes [η-1,2,4-(MeC)CH]Ln(CHCH--NMe) (Ln = Ce and La ), supported by a tri-butylcyclopentadienyl ligand, have been successfully synthesized. Studies demonstrate that these complexes possess diverse reactivity toward various small molecules. For example, the reaction of complexes and with diphenyl dichalcogenides PhEEPh (E = S, Se) results in the formation of lanthanide thiolates [(η-1,2,4-(MeC)CH)Ln(SPh)(μ-SPh)] (Ln = Ce and La ) and selenolates [(η-1,2,4-(MeC)CH)Ln(SePh)(μ-SePh)] (Ln = Ce and La ), concomitantly releasing PhE(CHCH--NMe).
View Article and Find Full Text PDFMacromol Rapid Commun
September 2024
Department of Chemical and Biological Engineering, Northwestern University, Evanston, IL, 60208, USA.
One method to improve the properties of covalent adaptable networks (CANs) is to reinforce them with a fraction of permanent cross-links without sacrificing their (re)processability. Here, a simple method to synthesize poly(n-hexyl methacrylate) (PHMA) and poly(n-lauryl methacrylate) (PLMA) networks containing static dialkyl disulfide cross-links (utilizing bis(2-methacryloyl)oxyethyl disulfide, or DSDMA, as a permanent cross-linker) and dynamic dialkylamino sulfur-sulfur cross-links (utilizing BiTEMPS methacrylate as a dissociative dynamic covalent cross-linker) is presented. The robustness and (re)processability of the CANs are demonstrated, including the full recovery of cross-link density after recycling.
View Article and Find Full Text PDFMolecules
May 2024
Hunan Province Key Laboratory for Synthetic Biology of Traditional Chinese Medicine, School of Pharmaceutical Sciences, Hunan University of Medicine, Huaihua 418000, China.
Thioethers are critical in the fields of pharmaceuticals and organic synthesis, but most of the methods for synthesis alkyl thioethers employ foul-smelling thiols as starting materials or generate them as by-products. Additionally, most thiols are air-sensitive and are easily oxidized to produce disulfides under atmospheric conditions; thus, a novel method for synthesizing thioethers is necessary. This paper reports a simple, effective, green method for synthesizing dialkyl or alkyl aryl thioether derivatives using odorless, stable, low-cost ROCSK as a thiol surrogate.
View Article and Find Full Text PDFJ Org Chem
December 2023
College of Chemistry and Chemical Engineering, Yangtze Normal University, Chongqing 408000, China.
Enter search terms and have AI summaries delivered each week - change queries or unsubscribe any time!