Cu(OTf)2-catalyzed asymmetric Friedel-Crafts alkylation reaction of indoles with arylidene malonates using bis(sulfonamide)-diamine ligands.J Org Chem. 2013 Jun 07; 78(11):5611-7.JO
Abstract
A highly efficient Cu-catalyzed asymmetric Friedel-Crafts alkylation reaction of indoles with arylidene malonates using simple, stable, and easily prepared bis-sulfonamide diamine ligands was developed. The desired products were obtained in up to 99% yield with 96% ee.
Links
Pub Type(s)
Journal Article
Research Support, Non-U.S. Gov't
Language
eng
PubMed ID
23642187
Citation
Wu, Jing, et al. "Cu(OTf)2-catalyzed Asymmetric Friedel-Crafts Alkylation Reaction of Indoles With Arylidene Malonates Using Bis(sulfonamide)-diamine Ligands." The Journal of Organic Chemistry, vol. 78, no. 11, 2013, pp. 5611-7.
Wu J, Wang D, Wu F, et al. Cu(OTf)2-catalyzed asymmetric Friedel-Crafts alkylation reaction of indoles with arylidene malonates using bis(sulfonamide)-diamine ligands. J Org Chem. 2013;78(11):5611-7.
Wu, J., Wang, D., Wu, F., & Wan, B. (2013). Cu(OTf)2-catalyzed asymmetric Friedel-Crafts alkylation reaction of indoles with arylidene malonates using bis(sulfonamide)-diamine ligands. The Journal of Organic Chemistry, 78(11), 5611-7. https://doi.org/10.1021/jo400747d
Wu J, et al. Cu(OTf)2-catalyzed Asymmetric Friedel-Crafts Alkylation Reaction of Indoles With Arylidene Malonates Using Bis(sulfonamide)-diamine Ligands. J Org Chem. 2013 Jun 7;78(11):5611-7. PubMed PMID: 23642187.
* Article titles in AMA citation format should be in sentence-case
TY - JOUR
T1 - Cu(OTf)2-catalyzed asymmetric Friedel-Crafts alkylation reaction of indoles with arylidene malonates using bis(sulfonamide)-diamine ligands.
AU - Wu,Jing,
AU - Wang,Dongping,
AU - Wu,Fan,
AU - Wan,Boshun,
Y1 - 2013/05/13/
PY - 2013/5/7/entrez
PY - 2013/5/7/pubmed
PY - 2013/12/20/medline
SP - 5611
EP - 7
JF - The Journal of organic chemistry
JO - J Org Chem
VL - 78
IS - 11
N2 - A highly efficient Cu-catalyzed asymmetric Friedel-Crafts alkylation reaction of indoles with arylidene malonates using simple, stable, and easily prepared bis-sulfonamide diamine ligands was developed. The desired products were obtained in up to 99% yield with 96% ee.
SN - 1520-6904
UR - https://www.unboundmedicine.com/medline/citation/23642187/Cu_OTf_2_catalyzed_asymmetric_Friedel_Crafts_alkylation_reaction_of_indoles_with_arylidene_malonates_using_bis_sulfonamide__diamine_ligands_
L2 - https://doi.org/10.1021/jo400747d
DB - PRIME
DP - Unbound Medicine
ER -