Asymmetric autocatalysis triggered by carbon isotope (13C/12C) chirality.
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Asymmetric Induction by a Nitrogen (14) N/(15) N Isotopomer in Conjunction with Asymmetric AutocatalysisAsymmetric Strecker Reaction Arising from the Molecular Orientation of an Achiral Imine at the Single-Crystal Face: Enantioenriched l- and d-Amino Acids.The origin of biological homochirality.Mechanisms of autocatalysis.Chirality amplification and detection by tactoids of lyotropic chromonic liquid crystals.Sensing through signal amplification.Molecular basis for chiral selection in RNA aminoacylation.Etiology of potentially primordial biomolecular structures: from vitamin B12 to the nucleic acids and an inquiry into the chemistry of life's origin: a retrospective.Catalytic asymmetric synthesis of enantioenriched heterocycles bearing a C-CF3 stereogenic center.Competitive exclusion principle in ecology and absolute asymmetric synthesis in chemistry.Approaches towards molecular amplification for sensing.Generation of absolute controlled crystal chirality by the removal of crystal water from achiral crystal of nucleobase cytosine.Crystal Structure of the Isopropylzinc Alkoxide of Pyrimidyl Alkanol: Mechanistic Insights for Asymmetric Autocatalysis with Amplification of Enantiomeric Excess.Discrimination of cryptochirality in chiral isotactic polystyrene by asymmetric autocatalysisAsymmetric autocatalysis induced by meteoritic amino acids with hydrogen isotope chirality.Chirality transfer in propeller-shaped cyclen-calcium(II) complexes: metal-coordinating and ion-pairing anion procedures.Asymmetric autocatalysis triggered by oxygen isotopically chiral glycerin.Modeling spontaneous chiral symmetry breaking and deracemization phenomena: discrete versus continuum approaches.Spontaneous mirror symmetry breaking and origin of biological homochirality.Can the analyte-triggered asymmetric autocatalytic Soai reaction serve as a universal analytical tool for measuring enantiopurity and assigning absolute configuration?Asymmetric autocatalysis induced by cinnabar: observation of the enantioselective adsorption of a 5-pyrimidyl alkanol on the crystal surface.Highly Stereoselective Strecker Synthesis Induced by a Slight Modification of Benzhydrylamine from Achiral to Chiral.Absolute asymmetric synthesis in enantioselective autocatalytic reaction networks: theoretical games, speculations on chemical evolution and perhaps a synthetic option.A closer look at spontaneous mirror symmetry breaking in aldol reactions.Self-replication and amplification of enantiomeric excess of chiral multifunctionalized large molecules by asymmetric autocatalysis.The Viedma deracemization of racemic conglomerate mixtures as a paradigm of spontaneous mirror symmetry breaking in aggregation and polymerization.Amplification of enantiomeric excess, mirror-image symmetry breaking and kinetic proofreading in Soai reaction models with different oligomeric orders.Unusual reversal of enantioselectivity in the asymmetric autocatalysis of pyrimidyl alkanol triggered by chiral aromatic alkanols and amines.Deuterium- and Tritium-Labelled Compounds: Applications in the Life Sciences.Reversal of the sense of enantioselectivity between 1- and 2-aza[6]helicenes used as chiral inducers of asymmetric autocatalysis.Emergence of chiral environments by effect of flows: the case of an ionic oligomer and Congo Red dye.Achiral Inorganic Gypsum Acts as an Origin of Chirality through Its Enantiotopic Surface in Conjunction with Asymmetric Autocatalysis.Point-to-Point Ultra-Remote Asymmetric Control with Flexible Linker.Replication of α-amino acids via Strecker synthesis with amplification and multiplication of chiral intermediate aminonitriles.Spontaneous formation and amplification of an enantioenriched α-amino nitrile: a chiral precursor for Strecker amino acid synthesis.The origin of isotope-induced helical-sense bias in supramolecular polymers of benzene-1,3,5-tricarboxamides.Temperature-controlled bidirectional enantioselectivity in a dynamic catalyst for asymmetric hydrogenation.Rationalization of Asymmetric Amplification via Autocatalysis Triggered by Isotopically Chiral Molecules.
P2860
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P2860
Asymmetric autocatalysis triggered by carbon isotope (13C/12C) chirality.
description
2009 nî lūn-bûn
@nan
2009年の論文
@ja
2009年学术文章
@wuu
2009年学术文章
@zh-cn
2009年学术文章
@zh-hans
2009年学术文章
@zh-my
2009年学术文章
@zh-sg
2009年學術文章
@yue
2009年學術文章
@zh
2009年學術文章
@zh-hant
name
Asymmetric autocatalysis triggered by carbon isotope (13C/12C) chirality.
@en
Asymmetric autocatalysis triggered by carbon isotope
@nl
type
label
Asymmetric autocatalysis triggered by carbon isotope (13C/12C) chirality.
@en
Asymmetric autocatalysis triggered by carbon isotope
@nl
prefLabel
Asymmetric autocatalysis triggered by carbon isotope (13C/12C) chirality.
@en
Asymmetric autocatalysis triggered by carbon isotope
@nl
P2093
P2860
P356
P1433
P1476
Asymmetric autocatalysis triggered by carbon isotope (13C/12C) chirality
@en
P2093
Kenso Soai
Kenta Suzuki
Masateru Ito
Takashi Tsutsumi
Yukari Matsumura
P2860
P304
P356
10.1126/SCIENCE.1170322
P407
P577
2009-03-26T00:00:00Z