Ir-catalyzed regio- and enantioselective Friedel-Crafts-type allylic alkylation of indoles.Org Lett. 2008 May 01; 10(9):1815-8.OL
Abstract
Highly regio- and enantioselective Ir-catalyzed Friedel-Crafts type allylic alkylation of indoles have been realized using [Ir(COD)Cl]2/phosphoramidite ligand 1a, affording the branched products with up to >97/3 branched-linear ratio and 92% ee.
Links
Pub Type(s)
Journal Article
Research Support, Non-U.S. Gov't
Language
eng
PubMed ID
18386906
Citation
Liu, Wen-Bo, et al. "Ir-catalyzed Regio- and Enantioselective Friedel-Crafts-type Allylic Alkylation of Indoles." Organic Letters, vol. 10, no. 9, 2008, pp. 1815-8.
Liu WB, He H, Dai LX, et al. Ir-catalyzed regio- and enantioselective Friedel-Crafts-type allylic alkylation of indoles. Org Lett. 2008;10(9):1815-8.
Liu, W. B., He, H., Dai, L. X., & You, S. L. (2008). Ir-catalyzed regio- and enantioselective Friedel-Crafts-type allylic alkylation of indoles. Organic Letters, 10(9), 1815-8. https://doi.org/10.1021/ol800409d
Liu WB, et al. Ir-catalyzed Regio- and Enantioselective Friedel-Crafts-type Allylic Alkylation of Indoles. Org Lett. 2008 May 1;10(9):1815-8. PubMed PMID: 18386906.
* Article titles in AMA citation format should be in sentence-case
TY - JOUR
T1 - Ir-catalyzed regio- and enantioselective Friedel-Crafts-type allylic alkylation of indoles.
AU - Liu,Wen-Bo,
AU - He,Hu,
AU - Dai,Li-Xin,
AU - You,Shu-Li,
Y1 - 2008/04/03/
PY - 2008/4/5/pubmed
PY - 2008/8/8/medline
PY - 2008/4/5/entrez
SP - 1815
EP - 8
JF - Organic letters
JO - Org Lett
VL - 10
IS - 9
N2 - Highly regio- and enantioselective Ir-catalyzed Friedel-Crafts type allylic alkylation of indoles have been realized using [Ir(COD)Cl]2/phosphoramidite ligand 1a, affording the branched products with up to >97/3 branched-linear ratio and 92% ee.
SN - 1523-7060
UR - https://www.unboundmedicine.com/medline/citation/18386906/Ir_catalyzed_regio__and_enantioselective_Friedel_Crafts_type_allylic_alkylation_of_indoles_
DB - PRIME
DP - Unbound Medicine
ER -