13295-94-8Relevant articles and documents
Nickel-catalyzed decarboxylative coupling of an alkynyl carboxylic acid with aryl iodides
Son, Yujeong,Kim, Han-Sung,Lee, Ju-Hyeon,Jang, Jisun,Lee, Chin-Fa,Lee, Sunwoo
, p. 1413 - 1416 (2017)
A decarboxylative coupling reaction with an alkynyl carboxylic acid and aryl iodides in the presence of a nickel catalyst was developed. When the reaction was conducted with NiCl2 (10?mol%), Xantphos (15?mol%), Mn (1.0?equiv), and Cs2CO3 (1.5?equiv), the desired diaryl alkynes were formed in moderated to good yields. Furthermore, this method does not produce the diyne, which is formed in the homocoupling of alkynyl carboxylic acids.
Two-photon spectroscopy of cyclometalated iridium complexes
Edkins, Robert M.,Bettington, Sylvia L.,Goeta, Andres E.,Beeby, Andrew
, p. 12765 - 12770 (2011)
The near-infrared two-photon absorption (TPA) spectra of a series of cyclometalated iridium complexes have been measured. These complexes exhibit moderately large TPA cross-sections of approximately 20 GM at the biological relevant wavelength of 800 nm. A new complex has been designed and synthesised, and found to have an increased cross-section of 44 GM at 800 nm. Full photophysical characterisation of this complex is presented.
Copper(0) nanoparticle catalyzed Z-Selective Transfer Semihydrogenation of Internal Alkynes
Moran, Maria Jesus,Martina, Katia,Bieliunas, Vidmantas,Baricco, Francesca,Tagliapietra, Silvia,Berlier, Gloria,De Borggraeve, Wim M.,Cravotto, Giancarlo
supporting information, p. 2850 - 2860 (2021/05/06)
The use of copper(0) nanoparticles in the transfer semihydrogenation of alkynes has been investigated as a lead-free alternative to Lindlar catalysts. A stereo-selective methodology for the hydrogenation of internal alkynes to the corresponding (Z)-alkenes in high isolated yields (86% average) has been developed. This green and sustainable transfer hydrogenation protocol relies on non-noble copper nanoparticles for reduction of both electron-rich and electron-deficient, aliphatic-substituted and aromatic- substituted internal alkynes. Polyols, such as ethylene glycol and glycerol, have been proven to act as hydrogen sources, and excellent stereo- and chemoselectivity have been observed. Enabling technologies, such as microwave and ultrasound irradiation are shown to enhance heat and mass transfer, whether used alone or in combination, resulting in a decrease in reaction time from hours to minutes. (Figure presented.).
Sequentially Pd/Cu-Catalyzed Alkynylation-Oxidation Synthesis of 1,2-Diketones and Consecutive One-Pot Generation of Quinoxalines
Niesobski, Patrik,Martínez, Ivette Santana,Kustosz, Sebastian,Müller, Thomas J. J.
supporting information, p. 5214 - 5218 (2019/07/31)
We report a simple and efficient one-pot synthesis of 1,2-diketones by concatenation of two Pd/Cu-catalyzed processes: Pd0/CuI-catalyzed Sonogashira coupling of terminal alkynes with aryl (pseudo)halides furnishes internal alkynes, which are directly transformed by PdII/CuII-catalyzed Wacker-type oxidation with DMSO and oxygen as dual oxidants to furnish 1,2-diketones. With this efficient, catalyst economical process, various aryl iodides and triflates are efficiently transformed in high yields into symmetrically and unsymmetrically substituted 1,2-diketones with various functional groups. This process can be readily extended to a consecutive one-pot synthesis of quinoxalines in a diversity-oriented fashion.
