Synthesis of multi-substituted dihydrofurans via palladium-catalysed coupling between 2,3-alkadienols and pronucleophiles
Literature Information
Hirokazu Tsukamoto, Kazuya Ito, Takayuki Doi
Multi-substituted dihydrofurans were obtained from a palladium-catalysed coupling reaction between 2,3-alkadienols and ketones bearing an electron-withdrawing group at the α-position. Methanol as a solvent was essential for the initial dehydrative substitution to suppress the competitive hydroalkylation of the diene moiety. The substitution would be followed by intramolecular hydroalkoxylation under the same catalysis.
Related Literature
Hydrogen storage characteristics of Li and Na decorated 2D boron phosphide
Younes Benhouria, Syeda R. Naqvi, Pritam K. Panda
DOI: 10.1039/D0SE00709A
Efficient and stable cycling of lithium metal enabled by a conductive carbon primer layer
Sheng S. Zhang, Xiulin Fan, Chunsheng Wang
DOI: 10.1039/C7SE00391A
Carbon onion–sulfur hybrid cathodes for lithium–sulfur batteries
Simon Fleischmann, Petr Formanek, Lars Borchardt
DOI: 10.1039/C6SE00034G
Cu3P/PAN derived N-doped carbon catalyst with non-toxic synthesis for alkaline hydrogen evolution reaction
HyoWon Kim, Yongju Lee, DongHoon Song, YongKeun Kwon, Eom-Ji Kim, EunAe Cho
DOI: 10.1039/D0SE00923G
Atomic layer deposition for perovskite solar cells: research status, opportunities and challenges
V. Zardetto, B. L. Williams, A. Perrotta, F. Di Giacomo, R. Andriessen
DOI: 10.1039/C6SE00076B
Drop-by-drop chemical reaction and sample introduction for capillary electrophoresis
Ying Rang, Ying Weng, Luyao Lin, Hulie Zeng, Hizuru Nakajim, Jin-Ming Lin, Katsumi Uchiyama
DOI: 10.1039/C5AN00040H
Effect of partial pressure on product selectivity in Cu-catalyzed electrochemical reduction of CO2
Mozhgan Moradzaman, Carlos Sánchez Martínez, Guido Mul
DOI: 10.1039/D0SE00865F
Asymmetric tin–vanadium redox electrolyte for hybrid energy storage with nanoporous carbon electrodes
Simon Fleischmann
DOI: 10.1039/C6SE00062B
Carbon-based materials as heterogeneous antioxidants for biodiesel: efficiency and synergy with soluble antioxidants
Tais da C. Soares, Paulo R. M. Silva, Gilberto A. Romeiro, Mauricio G. Fonseca, Luciano N. Batista
DOI: 10.1039/C6SE00017G
You might also like
Is 2-(2-chloroacetamido)-3-phenylpropanoic acid (CAS: 7765-11-9) safe?
2-(2-Chloroacetamido)-3-phenylpropanoic acid (CAS: 7765-11-9) is generally consi...
Is 2-(Benzyloxy)-5-bromobenzoic acid (CAS: 62176-31-2) safe?
2-(Benzyloxy)-5-bromobenzoic acid can be handled safely if appropriate precautio...
What is (4-Methyl-1,2,5-oxadiazol-3-yl)methanamine hydrochloride (CAS: 1159825-48-5)?
(4-Methyl-1,2,5-oxadiazol-3-yl)methanamine hydrochloride is a chemical compound ...
What is 2-(5-Hexylthiophen-2-yl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane (CAS: 917985-54-7)?
2-(5-Hexylthiophen-2-yl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane (CAS: 917985-54...
Are there alternatives to 4-(8-Methyl-9H-1,3-dioxolo[4,5-h][2,3]benzodiazepin-5-yl)benzenamine (CAS: 102771-26-6) in synthesis?
While 4-(8-Methyl-9H-1,3-dioxolo[4,5-h][2,3]benzodiazepin-5-yl)benzenamine (CAS:...
What is the market or research trend for tert-butyl 3-hydroxy-4,5,7,8-tetrahydro-2H-pyrazolo[3,4-d]azepine-6-carboxylate (CAS: 851376-80-2)?
The market for tert-butyl 3-hydroxy-4,5,7,8-tetrahydro-2H-pyrazolo[3,4-d]azepine...
How should waste containing 3,5-Diamino-1H-pyrazole-4-carbonitrile (CAS: 6844-58-2) be handled?
Waste containing 3,5-Diamino-1H-pyrazole-4-carbonitrile (CAS: 6844-58-2) should ...
How is (6-Fluoro-3-pyridinyl)boronic acid (CAS: 351019-18-6) typically synthesized?
(6-Fluoro-3-pyridinyl)boronic acid can be synthesized through the reaction of 6-...
What industries use Dibenzyl carbonimidoylbiscarbamate (CAS: 10065-79-9)?
Dibenzyl carbonimidoylbiscarbamate (CAS: 10065-79-9) finds applications in vario...
What is the market or research trend for (beta,beta,2,3,4,5,6-~2~H_7_)Phenylalanine (CAS: 74228-83-4)?
The market for (beta,beta,2,3,4,5,6-~2~H_7_)Phenylalanine (CAS: 74228-83-4) is g...
Source Journal
Chemical Communications

ChemComm publishes urgent research which is of outstanding significance and interest to experts in the field, while also appealing to the journal’s broad chemistry readership. Our communication format is ideally suited to short, urgent studies that are of such importance that they require accelerated publication. Our scope covers all topics in chemistry, and research at the interface of chemistry and other disciplines (such as materials science, nanoscience, physics, engineering and biology) where there is a significant novelty in the chemistry aspects. Major topic areas covered include: Analytical Chemistry Catalysis Chemical Biology and medicinal chemistry Computational Chemistry and Machine Learning Energy and sustainable chemistry Environmental Chemistry Green Chemistry Inorganic Chemistry Materials Chemistry Nanoscience Organic Chemistry Physical Chemistry Polymer Chemistry Supramolecular Chemistry














