Discrimination of cryptochirality in chiral isotactic polystyrene by asymmetric autocatalysis† †Electronic supplementary information (ESI) available: The asymmetric autocatalysis induced by bis(phenol) 5. See DOI: 10.1039/b912813a Click here for additional data file.
نویسندگان
چکیده
Chiral isotactic polystyrenes induce the enantioselective addition of diisopropylzinc to pyrimidine-5-carbaldehyde, affording the enantiomerically enriched pyrimidyl alkanol with the corresponding absolute configuration to that of cryptochiral polystyrenes in conjunction with asymmetric autocatalysis.
منابع مشابه
Asymmetric autocatalysis induced by meteoritic amino acids with hydrogen isotope chirality† †This article is part of a ChemComm ‘Catalysis in Organic Synthesis’ web-theme issue showcasing high quality research in organic chemistry. Please see our website (http://www.rsc.org/chemcomm/organicwebtheme2009) to access the other papers in this issue. ‡ ‡Electronic supplementary information (ESI) available: Procedures for the asymmetric autocatalysis in the presence of 1 and 2, the preparation of enantiomers of 1 and 2, and the determination of the enantiomeric purity of 1 and 2. See DOI: 10.1039/b908754k Click here for additional data file.
Achiral meteoritic amino acids, glycine and alpha-methylalanine, with hydrogen isotope (D/H) chirality, acted as the source of chirality in asymmetric autocatalysis with amplification of ee to afford highly enantioenriched 5-pyrimidyl alkanols.
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For the first time, a-formyldiazoacetates have been successfully applied for the asymmetric cyclopropanation of alkenes via Co(II)-based metalloradical catalysis. The cobalt(II) complex of the D2symmetric chiral amidoporphyrin [Co(3,5-DiBu-ChenPhyrin)] is an effective metalloradical catalyst that can activate a-formyldiazoacetates to cyclopropanate both aromatic and aliphatic olefins with varie...
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