Self-Replication and Amplification of Enantiomeric Excess of Chiral Multifunctionalized Large Molecules by Asymmetric Autocatalysis

2014 ◽  
Vol 53 (42) ◽  
pp. 11199-11202 ◽  
Author(s):  
Tsuneomi Kawasaki ◽  
Mai Nakaoda ◽  
Yutaro Takahashi ◽  
Yusuke Kanto ◽  
Nanako Kuruhara ◽  
...  
Keyword(s):  
Enantiomeric Excess ◽  
Large Molecules ◽  
Asymmetric Autocatalysis ◽  
Self Replication

Self-Replication and Amplification of Enantiomeric Excess of Chiral Multifunctionalized Large Molecules by Asymmetric Autocatalysis

2014 ◽  
Vol 126 (42) ◽  
pp. 11381-11384 ◽  
Author(s):  
Tsuneomi Kawasaki ◽  
Mai Nakaoda ◽  
Yutaro Takahashi ◽  
Yusuke Kanto ◽  
Nanako Kuruhara ◽  
...  
Keyword(s):  
Enantiomeric Excess ◽  
Large Molecules ◽  
Asymmetric Autocatalysis ◽  
Self Replication

scholarly journals Crystal Structure of the Isopropylzinc Alkoxide of Pyrimidyl Alkanol: Mechanistic Insights for Asymmetric Autocatalysis with Amplification of Enantiomeric Excess

2015 ◽  
Vol 54 (50) ◽  
pp. 15218-15221 ◽  
Author(s):  
Arimasa Matsumoto ◽  
Takaaki Abe ◽  
Atsushi Hara ◽  
Takayuki Tobita ◽  
Taisuke Sasagawa ◽  
...  
Keyword(s):  
Crystal Structure ◽  
Enantiomeric Excess ◽  
Asymmetric Autocatalysis

Asymmetric autocatalysis of 5-carbamoyl-3-pyridyl alkanols with amplification of enantiomeric excess

2000 ◽  
Vol 11 (21) ◽  
pp. 4249-4253 ◽  
Author(s):  
Shigehisa Tanji ◽  
Yasutaka Kodaka ◽  
Atsushi Ohno ◽  
Takanori Shibata ◽  
Itaru Sato ◽  
...  
Keyword(s):  
Enantiomeric Excess ◽  
Asymmetric Autocatalysis

scholarly journals Asymmetric autocatalysis triggered by triglycine sulfate with switchable chirality by the direction of electric field

2021 ◽  
Author(s):  
Tsuneomi Kawasaki ◽  
Yoshiyasu Kaimori ◽  
Seiya Shimada ◽  
Natsuki Hara ◽  
Susumu Sato ◽  
...  
Keyword(s):  
Electric Field ◽  
Organic Compounds ◽  
Enantiomeric Excess ◽  
Triglycine Sulfate ◽  
Molecular Chirality ◽  
Asymmetric Autocatalysis ◽  
Soai Reaction

Triglycine sulfate (TGS) acts as a chiral trigger for asymmetric autocatalysis with amplification of enantiomeric excess, i.e., the Soai reaction. Therefore, molecular chirality of highly enantioenriched organic compounds is controlled...

ChemInform Abstract: Asymmetric Autocatalysis of 5-Carbamoyl-3-pyridyl Alkanols with Amplification of Enantiomeric Excess.

ChemInform ◽  
2001 ◽  
Vol 32 (14) ◽  
pp. no-no
Author(s):  
Shigehisa Tanji ◽  
Yasutaka Kodaka ◽  
Atsushi Ohno ◽  
Takanori Shibata ◽  
Itaru Sato ◽  
...  
Keyword(s):  
Enantiomeric Excess ◽  
Asymmetric Autocatalysis

Relationship between the time, yield, and enantiomeric excess of asymmetric autocatalysis of chiral 2-alkynyl-5-pyrimidyl alkanol with amplification of enantiomeric excess

2003 ◽  
Vol 14 (8) ◽  
pp. 975-979 ◽  
Author(s):  
Itaru Sato ◽  
Daisuke Omiya ◽  
Hiroyoshi Igarashi ◽  
Keiichi Kato ◽  
Yoshihiro Ogi ◽  
...  
Keyword(s):  
Enantiomeric Excess ◽  
Asymmetric Autocatalysis
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