Abstract. Recent kinetic studies are discussed that shed light on the reaction mechanism of the autocatalytic addition of diisopropylzinc to pyrimidine carbaldehydes (Soai reaction). Soai’s reaction stands for the exclusive example of chirally autocatalytic reaction system in organic chemistry and has attracted close attention from several view-points: as possible account for the origin of biomolecular homochiral-ity, as potential innovation in enantioselective synthesis or as a fur-ther remarkable manifestation of nonlinear dynamics in chemical sys-tems. It is indicated that the reaction is driven by enantioselective autocatalysis and mutual inhibition as the essential components. A numerical approach reveals that experimentally observed c...
Several theories of asymmetric autocatalysis have been developed in the last decades. The major goal...
The only known example of chiral autocatalysis is the alkylation of N-heterocyclic aldehydes with iP...
For over 25 years the chemistry community has puzzled over the mechanism of the Soai reaction, a fas...
The autocatalytic, asymmetry-amplifying alkylation of pyrimidine-5-carbaldehydes with diisopropylzin...
Soai’s discovery of chiral amplification in the autocatalytic alkylation of pyrimidine-5-carbaldehyd...
The mechanism of the Soai reaction has been thoroughly investigated at the M05-2X/6-31G(d) level of ...
The Soai reaction has profoundly impacted chemists' perspective of autocatalysis, chiral symmetry br...
Chemical reactions that lead to a spontaneous symmetry breaking or amplification of the enantiomeric...
From a kinetic analysis of the “dimer model”, which is the most prominent mechanism of the Soai reac...
A kinetic model of spontaneous amplification of enantiomeric excess in the autocatalytic addition of...
Mechanisms leading to a molecular evolution and the formation of homochirality in nature are interco...
Diisopropylzinc alkylation of pyrimidine aldehydes-the Soai reaction, with its astonishing attribute...
Asymmetric amplification induced in the Soai autocatalytic reaction by chiral initiators that are en...
Absolute asymmetric synthesis (AAS) is the preparation of pure (or excess of one) enantiomer of a ch...
Several theories of asymmetric autocatalysis have been developed in the last decades. The major goal...
The only known example of chiral autocatalysis is the alkylation of N-heterocyclic aldehydes with iP...
For over 25 years the chemistry community has puzzled over the mechanism of the Soai reaction, a fas...
The autocatalytic, asymmetry-amplifying alkylation of pyrimidine-5-carbaldehydes with diisopropylzin...
Soai’s discovery of chiral amplification in the autocatalytic alkylation of pyrimidine-5-carbaldehyd...
The mechanism of the Soai reaction has been thoroughly investigated at the M05-2X/6-31G(d) level of ...
The Soai reaction has profoundly impacted chemists' perspective of autocatalysis, chiral symmetry br...
Chemical reactions that lead to a spontaneous symmetry breaking or amplification of the enantiomeric...
From a kinetic analysis of the “dimer model”, which is the most prominent mechanism of the Soai reac...
A kinetic model of spontaneous amplification of enantiomeric excess in the autocatalytic addition of...
Mechanisms leading to a molecular evolution and the formation of homochirality in nature are interco...
Diisopropylzinc alkylation of pyrimidine aldehydes-the Soai reaction, with its astonishing attribute...
Asymmetric amplification induced in the Soai autocatalytic reaction by chiral initiators that are en...
Absolute asymmetric synthesis (AAS) is the preparation of pure (or excess of one) enantiomer of a ch...
Several theories of asymmetric autocatalysis have been developed in the last decades. The major goal...
The only known example of chiral autocatalysis is the alkylation of N-heterocyclic aldehydes with iP...
For over 25 years the chemistry community has puzzled over the mechanism of the Soai reaction, a fas...