Search Results:　 1-8 of 8

Ukaji Yutaka , Inomata Katsuhiko

… In order to develop a practical method for the construction of chiral molecules, we have designed a novel chiral reaction system possessing multi-metal centers utilizing tartaric acid ester as a chiral auxiliary. … Based on this concept, we have developed an asymmetric 1,3-dipolar cycloaddition reaction of azomethine imines, an asymmetric hetero Diels-Alder reaction of nitroso compounds, an asymmetric Diels-Alder reaction of o-quinodimethanes. …

Chem. Rec. 10(3), 173-187, 2010-06-00

IR CrossRef Cited by (2)

KUBO Yuji

… The focus is on preparation and some intriguing properties of several kinds of azomethine-derived calixarenes : this work is extended in two related directions, the incorporation of indoaniline-type chromophores as an appropriate optical sensory group into calixarenes bearing a guest-binding site produced new types of receptors for optical sensing against cations. …

Journal of Synthetic Organic Chemistry, Japan 55(6), 506-516, 1997-06-01

J-STAGE CrossRef References (38)

Tachibana Yoji , Ando Makoto , Kuzuhara Hiroyoshi

… through Zn<SUP>2+</SUP>-catalyzed transamination reaction between the chiral pyridoxamine analogs, (<I>R</I>)- or (<I>S</I>)-15-aminomethyl-14-hydroxy-5,5-dimethyl-2,8-dithia[9] (2,5)pyridinophane and various α-keto acids with enantiomeric excesses ranging from 40 to 94%. …

Bulletin of the Chemical Society of Japan 56(12), 3652-3656, 1983

J-STAGE CrossRef