Acceleration and regioselectivity switching in 1,3-dipolar cycloaddition reactions confined in a bis-calix[4]pyrrole cage. [PDF]
Li Y, Aragay G, Ballester P.
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Synthesis of bioactive fluoropyrrolidines via copper(i)-catalysed asymmetric 1,3-dipolar cycloaddition of azomethine ylides. [PDF]
Xu X +6 more
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Microscopic mechanism of light-induced tetrazole-quinone 1,3-dipolar cycloaddition: a MS-CASPT2 theoretical investigation. [PDF]
He Y +6 more
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Diversitätsorientierte Synthese bioaktiver Allocolchicinoide und Colchicinoide unter Verwendung Übergangsmetall-katalysierter Cycloadditionen [PDF]
Nicolaus, Norman
core
Activator free diastereoselective 1,3-dipolar cycloaddition: a quick access to coumarin based spiro multi heterocyclic adducts. [PDF]
Thadem N, Rajesh M, Das S.
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Atroposelective Synthesis of Axially Chiral Naphthylpyrroles by a Catalytic Asymmetric 1,3-Dipolar Cycloaddition/Aromatization Sequence. [PDF]
Maclean I +6 more
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The Rich Chemistry Resulting from the 1,3‐Dipolar Cycloaddition Reactions of Enamines and Azides
V. Bakulev +3 more
semanticscholar +1 more source
Density Functional Theory Calculations: A Useful Tool to Investigate Mechanisms of 1,3-Dipolar Cycloaddition Reactions. [PDF]
Chiacchio MA, Legnani L.
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