Results 141 to 150 of about 2,089,289 (186)
[3 + 2]-Cycloaddition reaction of sydnones with alkynes. [PDF]
Beilstein J Org Chem, 2018 Hladíková V, Váňa J, Hanusek J.
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Mechanistic Studies of CO2 Cycloaddition Reaction Catalyzed by Amine-Functionalized Ionic Liquids. [PDF]
Front Chem, 2019 Chen J +6 more
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Investing in entropy: the strategy of cucurbit[n]urils to accelerate the intramolecular Diels-Alder cycloaddition reaction of tertiary furfuryl amines. [PDF]
Chem Scide la Vega-Hernández K +2 more
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2010
This chapter deals with enantioselective organocatalytic cycloaddition reactions. Several cinchona alkaloids have been recently demonstrated as efficient chiral organocatalysts for enantioselective Diels−Alder reactions. Thus, excellent results were obtained for the Diels−Alder reaction of 3-vinylindoles with maleimides catalysed by a ...
S. Araki, T. Hirashita
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This chapter deals with enantioselective organocatalytic cycloaddition reactions. Several cinchona alkaloids have been recently demonstrated as efficient chiral organocatalysts for enantioselective Diels−Alder reactions. Thus, excellent results were obtained for the Diels−Alder reaction of 3-vinylindoles with maleimides catalysed by a ...
S. Araki, T. Hirashita
+4 more sources
Retro‐Cycloaddition Reaction of Pyrrolidinofullerenes.
ChemInform, 2005AbstractChemInform 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.
Nazario, Martín +5 more
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Flow Chemistry for Cycloaddition Reactions
ChemSusChem, 2020AbstractAbstract: Continuous flow reactors form part of a rapidly growing research area that has changed the way synthetic chemistry is performed not only in academia but also at the industrial level. This Review highlights the most recent advances in cycloaddition reactions performed in flow systems.
Jorge, García-Lacuna +2 more
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2015
This chapter considers cycloadditions as the most useful of all pericyclic reactions in organic synthesis. It describes the wide range of known cycloadditions, identifies the conditions under which they take place, draws attention to their regio- and stereochemistry, and gives the simple rules for which of them take place and which do not.
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This chapter considers cycloadditions as the most useful of all pericyclic reactions in organic synthesis. It describes the wide range of known cycloadditions, identifies the conditions under which they take place, draws attention to their regio- and stereochemistry, and gives the simple rules for which of them take place and which do not.
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Selectivity in an Encapsulated Cycloaddition Reaction
Organic Letters, 2002A 1,3-dipolar cycloaddition takes place within a reversibly formed, self-assembled capsule. The reaction proceeds through an unsymmetrically loaded encapsulation complex with absolute regioselectivity.
Jian, Chen, Julius, Rebek
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