Enantioselective Friedel-Crafts alkylation of indoles with 2-enoylpyridine-N-oxides catalyzed by glucoBOX-Cu(II) complex.Org Biomol Chem. 2012 Jun 28; 10(24):4731-8.OB
Abstract
The glucosamine derived glucoBOX-Cu(II) complex was found to be a unique catalytic system for enantioselective Friedel-Crafts alkylation of indoles with 2-enoylpyridine-1-oxides. A large number of 3-alkylated indole derivatives were prepared using 5 mol% glucoBOX-Cu(II) complex in excellent yields with high enantioselectivity up to 99% ee.
Links
MeSH
Pub Type(s)
Journal Article
Research Support, Non-U.S. Gov't
Language
eng
PubMed ID
22585295
Citation
George, Jimil, and B V Subba Reddy. "Enantioselective Friedel-Crafts Alkylation of Indoles With 2-enoylpyridine-N-oxides Catalyzed By glucoBOX-Cu(II) Complex." Organic & Biomolecular Chemistry, vol. 10, no. 24, 2012, pp. 4731-8.
George J, Reddy BV. Enantioselective Friedel-Crafts alkylation of indoles with 2-enoylpyridine-N-oxides catalyzed by glucoBOX-Cu(II) complex. Org Biomol Chem. 2012;10(24):4731-8.
George, J., & Reddy, B. V. (2012). Enantioselective Friedel-Crafts alkylation of indoles with 2-enoylpyridine-N-oxides catalyzed by glucoBOX-Cu(II) complex. Organic & Biomolecular Chemistry, 10(24), 4731-8. https://doi.org/10.1039/c2ob25315a
George J, Reddy BV. Enantioselective Friedel-Crafts Alkylation of Indoles With 2-enoylpyridine-N-oxides Catalyzed By glucoBOX-Cu(II) Complex. Org Biomol Chem. 2012 Jun 28;10(24):4731-8. PubMed PMID: 22585295.
* Article titles in AMA citation format should be in sentence-case
TY - JOUR
T1 - Enantioselective Friedel-Crafts alkylation of indoles with 2-enoylpyridine-N-oxides catalyzed by glucoBOX-Cu(II) complex.
AU - George,Jimil,
AU - Reddy,B V Subba,
Y1 - 2012/05/15/
PY - 2012/5/16/entrez
PY - 2012/5/16/pubmed
PY - 2012/9/18/medline
SP - 4731
EP - 8
JF - Organic & biomolecular chemistry
JO - Org Biomol Chem
VL - 10
IS - 24
N2 - The glucosamine derived glucoBOX-Cu(II) complex was found to be a unique catalytic system for enantioselective Friedel-Crafts alkylation of indoles with 2-enoylpyridine-1-oxides. A large number of 3-alkylated indole derivatives were prepared using 5 mol% glucoBOX-Cu(II) complex in excellent yields with high enantioselectivity up to 99% ee.
SN - 1477-0539
UR - https://www.unboundmedicine.com/medline/citation/22585295/Enantioselective_Friedel_Crafts_alkylation_of_indoles_with_2_enoylpyridine_N_oxides_catalyzed_by_glucoBOX_Cu_II__complex_
L2 - https://doi.org/10.1039/c2ob25315a
DB - PRIME
DP - Unbound Medicine
ER -