| Literature DB >> 25873417 |
Shin A Moteki1, Hiroki Maruyama1, Keiji Nakayama1, Hai-Bei Li2,3, Galina Petrova2, Satoshi Maeda4, Keiji Morokuma5, Keiji Maruoka6.
Abstract
The origin of higher reactivity in water-accelerated asymmetric aldol reactions with our designed primary amine organocatalyst was elucidated by both computational and experimental methods. As suggested by the calculated transition-state structures for water-promoted imine-enamine isomerization, anti-selective aldol reaction and hemiaminal formation, the rate of this aldol reaction was found experimentally to be even more accelerated by the addition of cis-2-butene-1,4-diol as additive.Entities:
Keywords: aldol; amine; computation; organocatalysis; water
Year: 2015 PMID: 25873417 DOI: 10.1002/asia.201500078
Source DB: PubMed Journal: Chem Asian J ISSN: 1861-471X