The PtCl2-catalyzed cycloisomerization of allenyne systems has been examined. This process is a highly versatile tool for obtaining products that cannot be attainable with other metals. Simple adjustment of the allene or alkyne substitution can direct the reactivity in a selective manner and give birth to important carbocyclic frameworks (hydrindenes, cyclic vinylallenes, and trienes).
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http://dx.doi.org/10.1021/ja031892g | DOI Listing |
J Org Chem
November 2024
Key Laboratory of Drug-Targeting and Drug Delivery System of the Education Ministry and Sichuan Province, Sichuan Engineering Laboratory for Plant-Sourced Drug and Sichuan Research Center for Drug Precision Industrial Technology, West China School of Pharmacy, Sichuan University, Chengdu 610041, China.
Indene and furanone are important ring structures widely present in active pharmaceutical molecules. Here, we have developed a straightforward method for the synthesis of indene and furanone via PtCl-catalyzed intramolecular cyclization of α-benzyl allenoates. By altering the ester substitution pattern in the α-benzyl allenoates, we can regulate the reaction site, enabling two distinct intramolecular cyclization reactions that yield both indene and furanone products, respectively.
View Article and Find Full Text PDFDalton Trans
November 2024
Phosphorus Laboratory, Department of Chemistry, Indian Institute of Technology, Bombay, Powai, Mumbai 400076, India.
In this article, the synthesis of bis(phosphine), -PhPCHC(O)N(H)CHCHPPh- (1) (hereafter referred to as "PNHP" and its anionic form as "PNP") and its group 10 metal chemistry and catalytic studies are described. PNHP (1) on reaction with NiCl(DME) and PdCl(COD) afforded pincer complexes, [MCl{(PNP)κ-,,}] (M = Ni, 2; Pd, 3). A similar reaction of 1 with PtCl(COD) yielded a chelate complex, [PtCl{(PNHP)κ-,}] (4), which on further treatment with LiHMDS produced the 1,2-azaphospholene-phosphine complex, [PtCl(Ph){(-P(Ph)CHCONCHCHPPh-)κ-,}] (5) P-C/P-N bond metathesis.
View Article and Find Full Text PDFInt J Biol Macromol
September 2022
State Key Laboratory of Metastable Materials Science and Technology, College of Materials Science and Engineering, Yanshan University, Qinhuangdao, 066004, China; Key Laboratory of Applied Chemistry, Nano-biotechnology Key Lab of Hebei Province, College of Environmental and Chemical Engineering, Yanshan University, Qinhuangdao 066004, China. Electronic address:
The development of nanozymes with enhanced catalytic activity has been drawing great interest. Lentinan with special structure may be used to prepare bimetallic nanomaterials to enhance their catalytic activity. Herein, lentinan stabilized PdPt dendritic nanoparticles (PdPt-LNT NDs) were prepared through reduction of NaPdCl and KPtCl with a molar ratio of 1:3 using lentinan as a biological template.
View Article and Find Full Text PDFMikrochim Acta
August 2021
A.N. Bach Institute of Biochemistry, Federal Research Centre "Fundamentals of Biotechnology", Russian Academy of Sciences, Leninsky Prospect 33, 119071, Moscow, Russia.
Platinum-containing nanozymes with peroxidase-mimicking activity (PMA) have found a broad application in bioanalytical methods and are potentially able to compete with enzymes as the labels. However, traditionally used methods for the synthesis of nanozymes result in only a small fraction of surface-exposed Pt atoms, which participate in catalysis. To overcome this limitation, we propose a new approach for the synthesis of nanozymes with the efficient dispersion of Pt atoms on particles' surfaces.
View Article and Find Full Text PDFChemistry
March 2021
Department of Chemistry, School of Science, Tokyo Institute of Technology, 2-12-1 Ookayama, Meguro-ku, Tokyo, 152-8551, Japan.
Polycyclic aromatic compounds consisting of four or five fused anthracene units were synthesized by PtCl -catalyzed cycloisomerization as novel long expanded helicenes. These compounds have helical structures with significant stacking of the terminal anthracene moieties at 0.33 nm interlayer distance.
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