Enantioselective Friedel-Crafts alkylation of indoles with nitroalkenes catalyzed by bifunctional tridentate bis(oxazoline)-Zn(II) complex.Org Lett. 2006 May 11; 8(10):2115-8.OL
Abstract
[reaction: see text] A more practical and efficient catalytic asymmetric Friedel-Crafts alkylation of indoles with nitroalkenes using bifunctional tridentate bis(oxazoline)-Zn(OTf)(2) as catalyst has been developed. Various types of the nitroalkylated indoles were obtained in excellent yields (85-99%) and high enantioselectivities (up to 98% ee).
Pub Type(s)
Journal Article
Language
eng
PubMed ID
16671795
Citation
Lu, Shao-Feng, et al. "Enantioselective Friedel-Crafts Alkylation of Indoles With Nitroalkenes Catalyzed By Bifunctional Tridentate bis(oxazoline)-Zn(II) Complex." Organic Letters, vol. 8, no. 10, 2006, pp. 2115-8.
Lu SF, Du DM, Xu J. Enantioselective Friedel-Crafts alkylation of indoles with nitroalkenes catalyzed by bifunctional tridentate bis(oxazoline)-Zn(II) complex. Org Lett. 2006;8(10):2115-8.
Lu, S. F., Du, D. M., & Xu, J. (2006). Enantioselective Friedel-Crafts alkylation of indoles with nitroalkenes catalyzed by bifunctional tridentate bis(oxazoline)-Zn(II) complex. Organic Letters, 8(10), 2115-8.
Lu SF, Du DM, Xu J. Enantioselective Friedel-Crafts Alkylation of Indoles With Nitroalkenes Catalyzed By Bifunctional Tridentate bis(oxazoline)-Zn(II) Complex. Org Lett. 2006 May 11;8(10):2115-8. PubMed PMID: 16671795.
* Article titles in AMA citation format should be in sentence-case
TY - JOUR
T1 - Enantioselective Friedel-Crafts alkylation of indoles with nitroalkenes catalyzed by bifunctional tridentate bis(oxazoline)-Zn(II) complex.
AU - Lu,Shao-Feng,
AU - Du,Da-Ming,
AU - Xu,Jiaxi,
PY - 2006/5/5/pubmed
PY - 2006/5/5/medline
PY - 2006/5/5/entrez
SP - 2115
EP - 8
JF - Organic letters
JO - Org Lett
VL - 8
IS - 10
N2 - [reaction: see text] A more practical and efficient catalytic asymmetric Friedel-Crafts alkylation of indoles with nitroalkenes using bifunctional tridentate bis(oxazoline)-Zn(OTf)(2) as catalyst has been developed. Various types of the nitroalkylated indoles were obtained in excellent yields (85-99%) and high enantioselectivities (up to 98% ee).
SN - 1523-7060
UR - https://www.unboundmedicine.com/medline/citation/16671795/Enantioselective_Friedel_Crafts_alkylation_of_indoles_with_nitroalkenes_catalyzed_by_bifunctional_tridentate_bis_oxazoline__Zn_II__complex_
DB - PRIME
DP - Unbound Medicine
ER -
