Diversitätsorientierte Synthese bioaktiver Allocolchicinoide und Colchicinoide unter Verwendung Übergangsmetall-katalysierter Cycloadditionen [PDF]
Nicolaus, Norman
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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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Eco-Friendly 1,3-Dipolar Cycloaddition Reactions on Graphene Quantum Dots in Natural Deep Eutectic Solvent. [PDF]
Giofrè SV +9 more
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Study on Regio- and Diastereoselectivity of the 1,3-Dipolar Cycloaddition Reaction of Azomethine Ylide with 2-(Benzo[d]thiazol-2-yl)-3-(aryl)acrylonitrile: Synthesis, Spectroscopic, and Computational Approach. [PDF]
Hussein EM +7 more
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Ethynyl-substituted benzosiloxaboroles: the role of C(π)⋯B interactions in their crystal packing and use in Cu(i)-catalyzed 1,3-dipolar cycloaddition. [PDF]
Pacholak P +5 more
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Asymmetric 1,3-Dipolar Cycloaddition Reactions
Chemical Reviews, 1998Kurt V., Gothelf, Karl Anker, Jørgensen
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Natural 1,3‐Dipolar Cycloadditions
Angewandte Chemie International Edition, 2015[3+2] in the wild: Biomimetic natural product syntheses and theoretical considerations have indicated that 1,3-dipolar cycloadditions take place in nature. Now, the structure, biosynthesis, and function of a heavily modified prenylated flavin cofactor have been elucidated.
Martin, Baunach, Christian, Hertweck
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Asymmetric 1,3-dipolar cycloadditions
Tetrahedron, 2007AbstractChemInform is a weekly Abstracting Service, delivering concise information at a glance that was extracted from about 200 leading journals. To access a ChemInform Abstract, please click on HTML or PDF.
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Von Huisgen 1,2) wurde 1963 die 1,3-dipolare Cycloaddition 3–5) als Reaktionsprinzip zum Aufbau von Heterocyclen systematisiert. Man versteht darunter die Addition eines 1,3-Dipols 1, der aus den verschiedenen Kombinationen von Kohlenstoff-, Stickstoff- und Sauerstoffatomen bestehen kann und vier nicht dienische π-Elektronen umfast, an eine ...
Thomas Laue, Andreas Plagens
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