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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.

Authors+Show Affiliations

State Key Laboratory of Organometallic Chemistry, Shanghai Institute of Organic Chemistry, Chinese Academy of Sciences, Shanghai, China.No affiliation info availableNo affiliation info availableNo affiliation info available

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 -
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