170751-34-5Relevant academic research and scientific papers
Nickelocene as an Air- And Moisture-Tolerant Precatalyst in the Regioselective Synthesis of Multisubstituted Pyridines
Cho, Il Young,Hong, Sung You,Jeon, Ji Hwan,Kim, Woo Gyum,Lee, Jeong Woo,Seo, Jeong Kon,Seo, Jongcheol
, p. 9328 - 9343 (2021/07/26)
Ni(COD)2-catalyzed cycloaddition reactions to access pyridines have been extensively studied. However, this catalyst typically requires drying procedures and inert-atmosphere techniques for the reactions. Herein, we report operationally simple nickel(0) c
Rhodium-Catalyzed [2+2+2] Cycloadditions of Diynes with Morita-Baylis-Hillman Adducts: A Stereoselective Entry to Densely Functionalized Cyclohexadiene Scaffolds
Fernández, Martí,Parera, Magda,Parella, Teodor,Lledó, Agustí,Le Bras, Jean,Muzart, Jacques,Pla-Quintana, Anna,Roglans, Anna
supporting information, p. 1848 - 1853 (2016/06/09)
A rhodium-catalyzed asymmetric synthesis of 5,5-disubstituted cyclohexa-1,3-dienes has been achieved by [2+2+2] cycloaddition reactions between diynes and Morita-Baylis-Hillman (M-B-H) adducts as unsaturated substrates. Products containing two adjacent ch
Preference of Ruthenium-Based Metathesis Catalysts toward Z- and E-Alkenes as a Guide for Selective Reactions to Alkene Stereoisomers
Lee, Jihong,Kim, Kyung Hwan,Lee, Ok Suk,Choi, Tae-Lim,Lee, Hee-Seung,Ihee, Hyotcherl,Sohn, Jeong-Hun
, p. 7591 - 7596 (2016/09/09)
As a guide for selective reactions toward either Z- or E-alkene in a metathesis reaction, the relative preference of metathesis Ru catalysts for each stereoisomer was determined by a method using time-dependent fluorescence quenching. We found that Ru-1 p
Highly enantioselective rhodium-catalyzed [2+2+2] cycloaddition of diynes to sulfonimines
Amatore, Muriel,Lebuf, David,Malacria, Max,Gandon, Vincent,Aubert, Corinne
supporting information, p. 4576 - 4579 (2013/05/22)
A new asymmetric [2+2+2] cycloaddition of diynes to sulfonimines under rhodium catalysis that provides the corresponding enantioenriched 1,2-dihydropyridines in good yields is described.
Iron-catalyzed, hydrogen-mediated reductive cyclization of 1,6-enynes and diynes: Evidence for bis(imino)pyridine ligand participation
Sylvester, Kevin T.,Chirik, Paul J.
supporting information; experimental part, p. 8772 - 8774 (2009/12/04)
(Chemical Equation Presented) The bis(imino)pyridine iron dinitrogen complex (iPrPDI)Fe(N2)2 catalyzes the hydrogen-mediated reductive cyclization of enynes and diynes with turnover frequencies comparable to those of established precious metal catalysts. Amino, oxygenated, and carbon-based substrates are readily cyclized to the corresponding hetero- and carbocycles with 5 mol % iron and 4 atm H2 at 23°C. Stoichiometric reactions between selected substrates and the iron compound under a N2 atmosphere established transfer dehydrogenation from an isopropyl aryl substituent to either the enyne or diyne substrate. In situ monitoring of the catalytic reaction by 1H NMR spectroscopy coupled with deuterium labeling experiments established rapid cyclization followed by turnoverlimiting hydrogenation. Copyright
