Results 121 to 130 of about 153,572 (317)
A ruthenium‐catalyzed azide–alkyne cycloaddition (RuAAC) reaction is reported for the synthesis of selenium‐substituted triazole products. Reaction regioselectivity is dependent on the identity of the non‐selenium substituent of the alkyne, which challenges the perceived understanding of RuAAC regioselectivity.
Frances E. Bugden +9 more
wiley +1 more source
A new one‐pot, dual catalytic strategy for the synthesis of polycyclic isoquinolinone‐fused quinoxalines from commercially available N‐(2‐acetamidophenyl)benzamides and 1,3‐diynes is reported. This transformation proceeds via Rh(III)/Pd(II)‐mediated sequential NH/CH activation/annulation. Detailed mechanistic studies elucidate the reaction pathway. A
Wei‐Jung Chiu +3 more
wiley +1 more source
Studies on Heteroaromaticity. XIX. Direct 1,3-Dipolar Cycloaddition of Hydroxamoyl Chlorides with Enamines [PDF]
Tadashi Sasaki, Toshiyuki Yoshioka
openalex +1 more source
Recent Advances in Ene Reactions with Carbon Enophiles
Recent advances in the classical intra‐ and intermolecular ene nexus with carbon enophiles (alkenes, alkynes, arynes, and allenes) show a considerable increase in structural complexity and an enormous potential for functional applications in polymer science.
Thomas J. J. Müller
wiley +1 more source
Cycloadditions of difluoromethylenecyclopropanes
Abstract The isomeric difluoromethylenecyclopropanes, 1 + 2 were allowed to react with various alkene and diene reagents in order to test the reactivity of these two species toward (2+2) and (2+4) cycloadditions. Reactions with 1,1-dichloro-2,2-difluoroethylene, butadiene, cyclopentadiene, furan and diphenylisobenzofuran were attempted.
Dept. of Chemistry, University of Florida, Gainesville, FL 32611, U.S.A. ( host institution ) +3 more
openaire +3 more sources
A mild, scalable electrocatalytic method for direct lactonization of benzylic alcohols to phthalides using N‐hydroxyphthalimide as a redox mediator is reported. This metal‐free process proceeds via a phthalimide‐N‐oxyl‐mediated hydrogen atom transfer mechanism, shows broad scope with good to excellent yields, and enables late‐stage functionalizations ...
Pietro Ronco +6 more
wiley +1 more source
Cycloaddition of Diphenylnitrilimine to 1,5-Benzodiazepines [PDF]
The cycloaddition reaction of diphenylnitrilimine on the 1,5-benzodiazepines has been studied. New molecules of triazolobenzodiazepines type have been isolated and characterized.
Rachid Zinber +4 more
doaj
A stereoselective one‐step (3 + 3)‐cycloaddition between in situ generated pyrrole‐3‐methides and carbonyl ylides has been developed using cooperative rhodium and chiral phosphoric acid catalysis. The reaction affords oxa‐bridged cyclohepta[1,2‐b]pyrroles bearing three stereogenic centers, including two quaternary ones, in high yields and ...
Philipp Stehr, Christoph Schneider
wiley +1 more source
Thermal [2 + 3] cycloaddition of imino compounds to 3-aroylaziridines. Synthesis of imidazolidines [PDF]
J. W. LOWN, J. P. Moser, Robert Westwood
openalex +1 more source
Unleashing the power of Ag(I)‐acetylides with LiCl/dimethyl sulfoxide (DMSO). The LiCl/DMSO mixture have an unexplored ability to dramatically increase the solubility of Ag(I)‐acetylides regardless of their molecular structure, which is explored to achieve high chemoselectivity in the Cu(I)‐catalyzed interrupted cycloaddition between organic azides, Ag(
Diego Seckler +8 more
wiley +1 more source

