Cycloaddition reactions of nitrosoalkenes, azoalkenes and nitrile oxides mediated by hydrotalcite [PDF]
, 2012 Mg:Al 3:1 hydrotalcite (Ht), used in catalytic quantities, promotes the generation of nitrosoalkenes, azoalkenes and nitrile oxides. These can be intercepted in situ by heterocycles and olefins in [4+2] and [3+2] cycloaddition reactions, producing ...
Lemos, A., Lourenço, J. P.
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Quantitative Dynamics of the N2O + C2H2 → Oxadiazole Reaction: A Model for 1,3-Dipolar Cycloadditions. [PDF]
ACS Omega, 2020 Liu Y, Li J.
europepmc +1 more source
Mechanistic impact of oxime formation accompanying 1,3-dipolar cycloadditions of nitrile oxides [PDF]
, 1989 Baran, Janusz, Mayr, Herbert
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1,3-Dipolar cycloadditions of acridine with nitrile oxides
ARKIVOC, 2002 Antonino Corsaro +5 more
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The [3 + 2]- and [5 + 2]-cycloadditions of the cyclohepta-2,4-dienyl cation [PDF]
, 1987 Heilmann, Werner +2 more
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Enantioselective intramolecular 1,3-dipolar cycloadditions of diazocarbonyl-derived oxidopyryliums
ARKIVOC, 2003 David M. Hodgson +2 more
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Competing [2 + 3] and [4 + 3] cycloadditions of C,N-diphenylnitrone with 1,3-dienes. Evidence for thermally nonequilibrated intermediates [PDF]
, 1989 Baran, Janusz, Mayr, Herbert
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Accessing trifluoromethylated SuFEx-able pyrazole <i>via</i> distortion-accelerated 1,3-dipolar cycloadditions. [PDF]
RSC AdvKhanal B, Feliciano MAM, Gold B.
europepmc +1 more source
Tunable Endo/Exo Selectivity in Direct Catalytic Asymmetric 1,3-Dipolar Cycloadditions with Polyfunctional Lewis Acid / Azolium-Aryloxide Catalysts. [PDF]
Angew Chem Int Ed EnglBürstner A +13 more
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Decarboxylative 1,3-dipolar cycloadditions of l-proline. [PDF]
RSC AdvDoraghi F +6 more
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