著者
KAWASAKI Tsuneomi UCHIDA Mizuki KAIMORI Yoshiyasu SASAGAWA Taisuke MATSUMOTO Arimasa SOAI Kenso
出版者
The Chemical Society of Japan
雑誌
Chemistry letters (ISSN:03667022)
巻号頁・発行日
vol.42, no.7, pp.711-713, 2013-07-05
参考文献数
44
被引用文献数
22

5-Pyrimidyl alkanol with an enantiomeric excess of up to >99.5% was formed using chiral crystals of achiral tris(2-hydroxyethyl) 1,3,5-benzenetricarboxylate as a chiral initiator. In the enantioselective addition of diisopropylzinc to pyrimidine-5-carbaldehyde, the helicity of the molecular arrangement of achiral tricarboxylate in the crystalline state could be successfully used as a source of chirality to afford enantioenriched alkanol in conjunction with asymmetric autocatalysis with amplification of enantiomeric excess.

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“Enantioselective Synthesis Induced by the Helical Molecular Arrangement in the Chiral Crystal of Achiral Tris(2-hydroxyethyl) 1,3,5-Benzenetricarboxylate in Conjunction with Asymmetric Autocatalysis”
“Enantioselective Synthesis Induced by the Helical Molecular Arrangement in the Chiral Crystal of Achiral Tris(2-hydroxyethyl) 1,3,5-Benzenetricarboxylate in Conjunction with Asymmetric Autocatalysis”

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