cycloaddition

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cycloaddition

(ˌsaɪkləʊəˈdɪʃən)
n
a type of pericyclic chemical reaction
Collins English Dictionary – Complete and Unabridged, 12th Edition 2014 © HarperCollins Publishers 1991, 1994, 1998, 2000, 2003, 2006, 2007, 2009, 2011, 2014
Translations
cycloaddition
References in periodicals archive ?
Yus, "1, 3-Dipolar cycloadditions of azomethine imines," Organic & Biomolecular Chemistry, vol.
Prato, "Functionalization of carbon nanotubes via 1,3-dipolar cycloadditions," Journal of Materials Chemistry, vol.
Bonnert, "A novel one-pot method for the preparation of pyrazoles by 1,3-dipolar cycloadditions of diazo compounds generated in situ," The Journal of Organic Chemistry, vol.
Houk, "Theory of 1,3-dipolar cycloadditions: Distortion/interaction and frontier molecular orbital models," Journal of the American Chemical Society, vol.
Houk, "Reactivity and regioselectivity in 1,3-dipolar cycloadditions of azides to strained alkynes and alkenes: a computational study," Journal of the American Chemical Society, vol.
Copper(I) catalyzed and copper-free azide-alkyne cycloadditions (CuAAC and CuFAAC) are one of the most widely used click reactions.
Fiedler, Preparation of a Resin-Based Chromium Catalyst for Effecting [6pi + 2pi] Cycloadditions of Allenes, Org.
Romines, "Direct synthesis of furans by 3 + 2 cycloadditions between rhodium(II) acetate stabilized carbenoids and acetylenes," Tetrahedron, vol.
Included are stereoselective oxidation and reduction methods; stereoselective additions; cyclizations; metatheses and different types of rearrangements; asymmetric transition-metal-catalyzed, organocatalyzed, and biocatalytic reactions; methods for the formation of carbon-heteroatom and heteroatom-heteroatom bonds like asymmetric hydroamination and reduction amination, carboamination and alkylative cyclization, cycloadditions with carbon-heteroatom bond formation, and stereoselective halogenations; and methods for the formation of carbon-sulfur and carbon-phosphorus bonds and asymmetric sulfoxidation.
Caramella, "Cycloadditions of nitrile oxides to the highly reactive n-acyl-2-oxa3-azanorborn-5-enes afford versatile cycloadducts and a convenient entry to highly functionalized derivatives," European Journal of Organic Chemistry, vol.
for the DielsAlder cycloadditions of 2'-hydroxychalcones [34].