Results 61 to 70 of about 1,432 (170)

Electrocyclic Ring‐Opening of 1,2,4‐Oxadiazole[4,5‐a]piridinium Chloride: a New Route to 1,2,4‐Oxadiazole Dienamino Compounds

ChemistryOpen, 2019
1,2,4‐Oxadiazole[4,5‐a]piridinium chloride adds nucleophiles to undergo electrocyclic ring opening affording 1,2,4‐oxadiazole dienamino derivatives. These pyridinium salts represent a special class of Zincke salts that are prone to rearrange when treated
Dr. Stefano Carella, Dr. Misal Giuseppe Memeo, Prof. Paolo Quadrelli   +2 more
doaj   +1 more source

Dynamic Catalytic Highly Enantioselective 1,3-Dipolar Cycloadditions. [PDF]

Angew Chem Int Ed Engl, 2021
Yildirim O, Grigalunas M, Brieger L, Strohmann C, Antonchick AP, Waldmann H.   +5 more
europepmc   +1 more source

SuFExable NH-Pyrazoles via 1,3-Dipolar Cycloadditions of Diazo Compounds with Bromoethenylsulfonyl Fluoride. [PDF]

J Org Chem, 2022
Yamanushkin P, Kaya K, Feliciano MAM, Gold B.   +3 more
europepmc   +1 more source

A Novel Cycloaddition Reaction of Thermally Generated Sulfenes

CHIMIA, 1992
The highly strained ?-sultine 4, resulting from the addition of SO2 to benzobenzvalene, is shown to undergo a thermal cycloreversion which gives 1H-indene-1-thiocarbaldehyde dioxide (6) as an intermediate and subsequently 1H-indene-1 ...
Ulrich Burger, Serge P. Schmidlin, Jiri Mareda, Gerald Bernardinelli   +3 more
doaj   +2 more sources

Acceleration of 1,3-Dipolar Cycloadditions by Integration of Strain and Electronic Tuning. [PDF]

J Am Chem Soc, 2021
Dones JM, Abularrage NS, Khanal N, Gold B, Raines RT.   +4 more
europepmc   +1 more source

Regio- and Diastereoselective 1,3-Dipolar Cycloadditions of 1,2,4-Triazin-1-ium Ylides: a Straightforward Synthetic Route to Polysubstituted Pyrrolo[2,1-f][1,2,4]triazines. [PDF]

ACS Omega, 2022
Galeta J, Šlachtová V, Dračínský M, Vrabel M.   +3 more
europepmc   +1 more source

Dimerization reactions of aryl selenophen-2-yl-substituted thiocarbonyl S-methanides as diradical processes: a computational study

Beilstein Journal of Organic Chemistry, 2017
An intriguing stepwise diradical mechanism of the dimerization of the reactive intermediate (thiocarbonyl S-methanide) appearing in the reaction of phenyl selenophen-2-yl thioketone with diazomethane was studied by means of computational methods.
Michael L. McKee, Grzegorz Mlostoń, Katarzyna Urbaniak, Heinz Heimgartner   +3 more
doaj   +1 more source

Nitropyridines as 2π-Partners in 1,3-Dipolar Cycloadditions with N-Methyl Azomethine Ylide: An Easy Access to Condensed Pyrrolines. [PDF]

Molecules, 2021
Bastrakov MA, Fedorenko AK, Starosotnikov AM, Shakhnes AK.   +3 more
europepmc   +1 more source

Multicomponent syntheses of pyrazoles via (3 + 2)-cyclocondensation and (3 + 2)-cycloaddition key steps

Beilstein Journal of Organic Chemistry
Pyrazoles are rarely found in nature but are traditionally used in the agrochemical and pharmaceutical industries, while other areas of use are also actively developing. However, they have also found numerous other applications.
Ignaz Betcke, Alissa C. Götzinger, Maryna M. Kornet, Thomas J. J. Müller   +3 more
doaj   +1 more source

Synthesis of chiral-at-metal rhodium complexes from achiral tripodal tetradentate ligands: resolution and application to enantioselective Diels-Alder and 1,3-dipolar cycloadditions. [PDF]

RSC Adv, 2022
Tejero AG, Carmona M, Rodríguez R, Viguri F, Lahoz FJ, García-Orduña P, Carmona D.   +6 more
europepmc   +1 more source