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.
Links
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 -