, 2016 Catalytic Enantioselective 1,3-Dipolar Cycloadditions between Nitrones and Alkenes Using a Novel Heterochiral Ytterbium(III ...
Shū Kobayashi (2450098) +1 more
core +1 more source
Acceleration of 1,3-Dipolar Cycloadditions by Integration of Strain and Electronic Tuning. [PDF]
J Am Chem Soc, 2021 Dones JM +4 more
europepmc +1 more source
An overview of the cycloaddition chemistry of fulvenes and emerging applications
Beilstein Journal of Organic Chemistry, 2019 The unusual electronic properties and unique reactivity of fulvenes have interested researchers for over a century. The propensity to form dipolar structures at relatively low temperatures and to participate as various components in cycloaddition ...
Ellen Swan +2 more
doaj +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 +3 more
europepmc +1 more source
Retro‐Hetero‐Michael Addition Strategies in Organic Synthesis
European Journal of Organic Chemistry, Volume 29, Issue 32, 24 August 2026.In this review, synthetic approaches to carbo‐ and heterocyclic compounds, including natural products, published in the last 15 years (2011–2025) which have either relied upon or included a retro‐hetero‐Michael addition step at any stage are discussed.
Dina Scarpi, Ernesto G. Occhiato
wiley +1 more source
Isotelluroureas for Asymmetric C1 Ammonium Enolate Reactions
European Journal of Organic Chemistry, Volume 29, Issue 31, 19 August 2026.Chiral isotelluroureas are powerful catalysts for a variety of C─C bond forming C1 ammonium enolate transformations. Isotelluroureas (ITeUs) have recently been introduced as a novel class of highly nucleophilic Lewis base catalysts. Herein, we systematically screened them for their potential to facilitate C1 ammonium enolate transformations and ...
Fereshteh Khorasani +3 more
wiley +1 more source
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 +2 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 +3 more
europepmc +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 +6 more
europepmc +1 more source
Phospha-munchnones: electronic structures and 1,3-dipolar cycloadditions
, 2010 The reaction of imines, acid chlorides, PR, and base generates a new class of 1,3-dipoles: phospha-Münchnones. These 1,3-dipoles can undergo cycloadditions with alkynes followed by loss of phosphine oxides to form pyrroles.
Belanger-Gariepy, Francine +5 more
core +1 more source