1114452-83-3Relevant academic research and scientific papers
Boryl Radical-Mediated C?H Activation of Inactivated Alkanes for the Synthesis of Internal Alkynes
Han, Jia-Bin,San, Htet Htet,Guo, Ao,Wang, Long,Tang, Xiang-Ying
, p. 2366 - 2370 (2020/11/30)
An intriguing pyridine-boryl radical-mediated C?H alkynylation reaction of inactivated alkanes was described. The reaction features mild operation condition and wide substrate scope, and affords the corresponding products in moderate to good yields. Notab
Visible light promoted coupling of alkynyl bromides and Hantzsch esters for the synthesis of internal alkynes
Song, Zhi-Yong,Zhang, Chun-Lin,Ye, Song
, p. 181 - 185 (2019/01/04)
A metal-free visible light promoted C(sp3)-C(sp) coupling reaction of alkynyl bromides and Hantzsch esters was developed, giving internal alkynes with primary, secondary, tertiary alkyl or other functional groups in good to high yields.
Multi-Metal-Catalyzed Oxidative Radical Alkynylation with Terminal Alkynes: A New Strategy for C(sp3)-C(sp) Bond Formation
Tang, Shan,Liu, Yichang,Gao, Xinlong,Wang, Pan,Huang, Pengfei,Lei, Aiwen
supporting information, p. 6006 - 6013 (2018/05/14)
A new way for C(sp3)-C(sp) cross-coupling with terminal alkynes has been developed by using a multi-metal-catalyzed reaction strategy. Alkyl radicals generated from different approaches are able to couple with terminal alkynes by judicious selection of the catalyst combination. This reaction protocol offers an efficient alternative approach for the synthesis of substituted alkynes from terminal alkynes besides traditional Sonogashira coupling. Mechanistic studies have also been carried out to clarify the role of each metal catalyst in the radical alkynylation processes. The reactions were found to go through radical reaction pathways. Synergistic cooperation of the metal catalysts is the key for controlling the reaction selectivity of alkyl radicals toward C(sp3)-C(sp) bond formation.
Synthesis and electrical properties of novel oligomer semiconductors for organic field-effect transistors (OFETs): Asymmetrically end-capped acene-heteroacene conjugated oligomers
Back, Jang Yeol,Kim, Yebyeol,An, Tae Kyu,Kang, Moon Seong,Kwon, Soon-Ki,Park, Chan Eon,Kim, Yun-Hi
, p. 220 - 226 (2014/08/18)
Noble small molecules composed of an aromatic phenylene-trithiophene and naphthalene-trithiophene conjugated core were synthesized and examined for their property in p-type OFET devices. The phenylene and naphthalene moieties were combined with a trithiophene to introduce torsional structures into the conjugated core and improve the solubility compared with the solubility of the quaterthiophene core containing molecule. Although phenylene-trithiophene and naphthalene-trithiophene containing molecules showed lower mobilities (2.9 × 10-3 and 1.04 × 10-2 cm2/V, respectively) than quaterthiophene containing molecule (3.21 × 10 -2 cm2/V), they showed more film uniformity caused by improved solubility. The thermal stability, photochemical properties, and morphological characteristics were investigated using TGA, DSC, cyclic voltammetry, and XRD techniques.
Sulfonated N-heterocyclic carbenes for Pd-catalyzed sonogashira and suzuki-miyaura coupling in aqueous solvents
Roy, Sutapa,Plenio, Herbert
experimental part, p. 1014 - 1022 (2010/06/17)
The reactions of the N, N-diarylimidazolium and N, N-diarylimidazolinium salts with chlorosulfonic acid result in the formation of the respective disulfonated N-heterocyclic carbene (NHC) precursors in reasonable yields (46-77%). Water-soluble palladium catalyst complexes, in situ obtained from the respective sulfonated imidazolinium salt, sodium tetrachloropalladate (Na 2PdCl4) and potassium hydroxide (KOH) in water, were successfully applied in the copper-free Sonogashira coupling reaction in isopropyl alcohol/water mixtures using 0.2 mol% catalyst loading. The preformed (disulfonatedNHC)PdCl(cinnamyl) complex was used in aqueous Suzuki-Miyaura reactions at 0.1 mol% catalyst loading. The coupling protocol reported here is very useful for Sonogashira reactions of N- and 5-heterocyclic aryl bromides and chlorides with aryl- and alkylacetylenes.
