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Asymmetric 1,2-reduction of enones with potassium borohydride catalyzed by chiral N,N'-dioxide-scandium(III) complexes.
Org Lett. 2012 Oct 05; 14(19):5134-7.OL

Abstract

The first catalytic enantioselective 1,2-reduction of enones with 0.45 mol equiv potassium borohydride solution catalyzed by a chiral N,N'-dioxide-Sc(III) complex catalyst was accomplished under mild reaction conditions. A number of optically active allylic alcohols were obtained in good to excellent enantioselectivities (up to 95% ee) with nearly quantitative yields.

Authors+Show Affiliations

Key Laboratory of Green Chemistry & Technology, Ministry of Education, College of Chemistry, Sichuan University, Chengdu 610064, P. R. China.No affiliation info availableNo affiliation info availableNo affiliation info availableNo affiliation info availableNo affiliation info available

Pub Type(s)

Journal Article

Language

eng

PubMed ID

23013322

Citation

He, Peng, et al. "Asymmetric 1,2-reduction of Enones With Potassium Borohydride Catalyzed By Chiral N,N'-dioxide-scandium(III) Complexes." Organic Letters, vol. 14, no. 19, 2012, pp. 5134-7.
He P, Liu X, Zheng H, et al. Asymmetric 1,2-reduction of enones with potassium borohydride catalyzed by chiral N,N'-dioxide-scandium(III) complexes. Org Lett. 2012;14(19):5134-7.
He, P., Liu, X., Zheng, H., Li, W., Lin, L., & Feng, X. (2012). Asymmetric 1,2-reduction of enones with potassium borohydride catalyzed by chiral N,N'-dioxide-scandium(III) complexes. Organic Letters, 14(19), 5134-7. https://doi.org/10.1021/ol302430h
He P, et al. Asymmetric 1,2-reduction of Enones With Potassium Borohydride Catalyzed By Chiral N,N'-dioxide-scandium(III) Complexes. Org Lett. 2012 Oct 5;14(19):5134-7. PubMed PMID: 23013322.
* Article titles in AMA citation format should be in sentence-case
TY - JOUR T1 - Asymmetric 1,2-reduction of enones with potassium borohydride catalyzed by chiral N,N'-dioxide-scandium(III) complexes. AU - He,Peng, AU - Liu,Xiaohua, AU - Zheng,Haifeng, AU - Li,Wei, AU - Lin,Lili, AU - Feng,Xiaoming, Y1 - 2012/09/26/ PY - 2012/9/28/entrez PY - 2012/9/28/pubmed PY - 2012/9/28/medline SP - 5134 EP - 7 JF - Organic letters JO - Org Lett VL - 14 IS - 19 N2 - The first catalytic enantioselective 1,2-reduction of enones with 0.45 mol equiv potassium borohydride solution catalyzed by a chiral N,N'-dioxide-Sc(III) complex catalyst was accomplished under mild reaction conditions. A number of optically active allylic alcohols were obtained in good to excellent enantioselectivities (up to 95% ee) with nearly quantitative yields. SN - 1523-7052 UR - https://www.unboundmedicine.com/medline/citation/23013322/Asymmetric_12_reduction_of_enones_with_potassium_borohydride_catalyzed_by_chiral_NN'_dioxide_scandium_III__complexes_ L2 - https://doi.org/10.1021/ol302430h DB - PRIME DP - Unbound Medicine ER -