| Literature DB >> 16003811 |
Yoshihiro Horiuchi1, Vijay Gnanadesikan, Takashi Ohshima, Hyuma Masu, Kosuke Katagiri, Yoshihisa Sei, Kentaro Yamaguchi, Masakatsu Shibasaki.
Abstract
The development of a direct catalytic asymmetric aldol-Tishchenko reaction and the nature of its catalyst are described. An aldol-Tishchenko reaction of various propiophenone derivatives with aromatic aldehydes was promoted by [LaLi3(binol)3] (LLB), and reactivity and enantioselectivity were dramatically enhanced by the addition of lithium trifluoromethanesulfonate (LiOTf). First, we observed a dynamic structural change of LLB by the addition of LiOTf using 13C NMR spectroscopy, electronspray ionization mass spectrometry (ESI-MS), and cold-spray ionization mass spectrometry (CSI-MS). X-ray crystallography revealed that the structure of the newly generated self-assembled complex was a binuclear [La2Li4(binaphthoxide)5] complex 6. A reverse structural change of complex 6 to LLB by the addition of one equivalent of Li2(binol) was also confirmed by ESI-MS and experimental results. The drastic concentration effects on the direct catalytic asymmetric aldol-Tishchenko reaction suggested that the addition of LiOTf to LLB generated an active oligomeric catalyst species.Entities:
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Year: 2005 PMID: 16003811 DOI: 10.1002/chem.200500442
Source DB: PubMed Journal: Chemistry ISSN: 0947-6539 Impact factor: 5.236