14309-57-0Relevant articles and documents
Asymmetric synthesis of 9-alkyl tetrahydroxanthenones: Via tandem asymmetric Michael/cyclization promoted by chiral phosphoric acid
Gao, Yu-Qi,Hou, Yi,Chen, Junhan,Zhen, Yanxia,Xu, Dongyang,Zhang, Hongli,Wei, Hongbo,Xie, Weiqing
supporting information, p. 348 - 354 (2021/01/29)
A tandem asymmetric Michael-addition/cyclization of cyclic 1,3-dicarbonyl compounds to β,γ-unsaturated α-ketoesters catalyzed by chiral phosphoric acid is presented. This protocol provides a facile approach for the construction of enantioenriched 9-alkyl tetrahydroxanthenones, an ubiquitous framework found in a number of natural products and pharmaceutical molecules, in high yields with good to high enantioselectivities. This journal is
Activation of Chiral (Salen)AlCl Complex by Phosphorane for Highly Enantioselective Cyanosilylation of Ketones and Enones
Zeng, Xing-Ping,Cao, Zhong-Yan,Wang, Xin,Chen, Long,Zhou, Feng,Zhu, Feng,Wang, Cui-Hong,Zhou, Jian
supporting information, p. 416 - 425 (2016/01/25)
Phosphoranes 2 are identified as a class of effective Lewis bases to activate chiral (salen)AlCl complex 1 to enhance its electrophilicity. Accordingly, a three-component catalyst system consisting of complex 1, phosphorane 2e, and Ph3PO is developed as a powerful tool for asymmetric ketone cyanosilylation. In particular, an unprecedented highly enantioselective cyanosilylation of linear aliphatic ketones is achieved. A tandem Wittig-cyanosilylation sequence starting from phosphorane 2a and enals 10 is further achieved, which internally utilizes the Ph3PO byproduct and remaining phosphorane 2a as cocatalysts for cyanosilylation of α,β,γ,δ-unsaturated enones, providing atom-efficient access to valuable chiral conjugated dienes and enynes. The high efficiency of the cyanosilylation originates from orthogonal activation of both (salen)AlCl complex 1 and cyanotrimethylsilane by the phosphorane and Ph3PO, respectively. This mechanistic insight is supported by NMR, MS, and ReactIR analyses and DFT calculations. Furthermore, the formation of charged complexes through the activation of chiral complex 1 by phosphorane 2a is confirmed by electrical conductivity experiments.
Control of aldol reaction pathways of enolizable aldehydes in an aqueous environment with a hyperbranched polymeric catalyst
Chi, Yonggui,Scroggins, Steven T.,Boz, Emine,Fre Chet, Jean M. J.
supporting information; experimental part, p. 17287 - 17289 (2009/07/11)
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