Results 131 to 140 of about 3,577 (190)
Asymmetric formal [1 + 2 + 2]-cycloaddition of diazoamides with enamines and carbonyl compounds. [PDF]
Dong S +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]
Hofer M +4 more
europepmc +1 more source
Influence of the Nature of Group 15 Element on [Au<sup>I</sup>]-C≡E/Azide 1,3-Dipolar Cycloaddition Reaction. [PDF]
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]
Matsubuchi H +6 more
europepmc +1 more source
Nanoparticle‐Catalysed 1,3‐Dipolar Cycloadditions [PDF]
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.
Alessandro Ponti, Giorgio Molteni
exaly +4 more sources
Asymmetric 1,3-dipolar cycloadditions of acrylamides
This critical review, which is relevant to researchers in synthetic organic chemistry, focuses on asymmetric 1,3-dipolar cycloadditions with acrylamides. The use of chiral acrylamides as dipolarophiles leads to high levels of stereocontrol, due to conformational constraint in the acrylamides.
Marie Kissane, Anita R Maguire
exaly +4 more sources
Transition Metal Complexation in 1,3-Dipolar Cycloadditions
AbstractFor Abstract see ChemInform Abstract in Full Text.
BROGGINI, GIANLUIGI +3 more
openaire +4 more sources
1,3-Dipolar cycloadditions of MeOPEG-bounded azides
1,3-Dipolar cycloadditions of MeOPEG-supported azide 2 with a variety of dipolarophiles have been studied. 1-MeOPEGsupported 1,2,3-triazoles 4 and 5, 1,2,3,4-tetrazoles 12 and aziridine 14 were obtained in nearly quantitative yields. The removal of the
Giorgio Molteni, Paola Del Buttero
exaly +2 more sources

