Results 111 to 120 of about 1,577 (174)

Understanding Bio-Orthogonal Strain-Driven Sydnone Cycloadditions: Data-Assisted Profiles and the Search for Linear Relationships. [PDF]

Molecules
García de la Concepción J, Cintas P, Martínez RF.   +2 more
europepmc   +1 more source

Regiodivergence in the Cycloadditions between a Cyclic Nitrone and Carbonyl-Type Dipolarophiles. [PDF]

J Org Chem
Esteban A, Nieto CT, Garrido NM, Sanz F, Díez D.   +4 more
europepmc   +1 more source

Synthetic Strategies of Fused Triazole Frameworks: A Comprehensive Review. [PDF]

ACS Omega
Tamminana R, Mohammed A.
europepmc   +1 more source

Thiophene Derivatives as Versatile Precursors for (Hetero)Arene and Natural Product Synthesis. [PDF]

Angew Chem Int Ed Engl
Keimer A, Haut FL.
europepmc   +1 more source

Asymmetric formal [1 + 2 + 2]-cycloaddition of diazoamides with enamines and carbonyl compounds. [PDF]

Nat Commun
Dong S, Yao M, Wang Y, Xie X, Jiang X, Xu X.   +5 more
europepmc   +1 more source

Asymmetric Isochalcogenourea-Catalyzed Synthesis of 3,4-Dihydropyrans via (4+2)-Cycloadditions of Ethyl But-3-ynoate with Michael Acceptors. [PDF]

Synlett
Hofer M, Piringer M, Scheucher A, Vogl LS, Waser M.   +4 more
europepmc   +1 more source

Influence of the Nature of Group 15 Element on [Au^I]-C≡E/Azide 1,3-Dipolar Cycloaddition Reaction. [PDF]

Inorg Chem
González-Pinardo D, Fernández I.
europepmc   +1 more source

Solvent Effects on the Selectivity of Ambimodal Dipolar/Diels-Alder Cycloadditions: A Study Using Explicit Solvation Models. [PDF]

Chemphyschem
Matsubuchi H, Hayashi D, Okamoto D, Noguchi A, Nakagawa S, Takayanagi T, Murakami T.   +6 more
europepmc   +1 more source

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Nanoparticle‐Catalysed 1,3‐Dipolar Cycloadditions

European Journal of Organic Chemistry, 2020
The 1,3‐dipolar cycloadditions of azomethine‐ylides and ‐imines, nitrones, nitrilimines, and azides catalysed by inorganic nanoparticles are described. Emphasis is given to the nanometric catalysts involved, their structure, characterisation, and recyclability and, when remarkable, their preparation.
Giorgio Molteni, Alessandro Ponti
exaly   +3 more sources