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Structure-Reactivity Relationship Studies for Guanidine-Organocatalyzed Direct Intramolecular Aldolization of Ketoaldehydes
Vise andre og tillknytning
2010 (engelsk)Inngår i: ChemCatChem, ISSN 1867-3880, E-ISSN 1867-3899, Vol. 2, nr 12, s. 1573-1581Artikkel i tidsskrift (Fagfellevurdert) Published
Abstract [en]

Structure-reactivity studies are performed to explore the reaction mechanism of the guanidine-catalyzed intramolecular aldol reaction of ketoaldehydes. A large number of guanidine and guanidine-like catalysts are synthesized and their properties studied. Kinetic profiles and pK(a) values of the catalysts are measured and correlated to reaction barriers calculated using density functional theory (DFT). The DFT calculations show that structural rigidity influences the pKa of the guanidines. Although the basicity is a very important factor in the catalysis, it is not sufficient to fully account for its catalytic efficiency. The availability of two aligned nitrogen reaction sites for proton shuttling in the transition state is an essential feature that helps to rationalize the reactivity pattern and the activation mode for this family of organocatalysts.

sted, utgiver, år, opplag, sider
2010. Vol. 2, nr 12, s. 1573-1581
Emneord [en]
aldolization, density functional calculations, organocatalysis, regioselectivity, structure-activity relationships
HSV kategori
Forskningsprogram
fysikalisk kemi
Identifikatorer
URN: urn:nbn:se:su:diva-51257DOI: 10.1002/cctc.201000227ISI: 000284717800014OAI: oai:DiVA.org:su-51257DiVA, id: diva2:385109
Forskningsfinansiär
Swedish Research Council
Merknad

authorCount :7

Tilgjengelig fra: 2011-01-11 Laget: 2011-01-10 Sist oppdatert: 2017-12-11bibliografisk kontrollert

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