Highly enantioselective Friedel–Crafts alkylation of indole with electron deficient trans-β-nitroalkenes using Zn(II)–oxazoline–imidazoline catalysts-Reference-Cited by-同舟云学术

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Highly enantioselective Friedel–Crafts alkylation of indole with electron deficient trans-β-nitroalkenes using Zn(II)–oxazoline–imidazoline catalysts

Published:2014-02 Issue:3 Volume:25 Page:245-251
ISSN:0957-4166
Container-title:Tetrahedron: Asymmetry
language:en
Short-container-title:Tetrahedron: Asymmetry

Author:

Islam Mohammad Shahidul,Al Majid Abdullah M.A.,Al-Othman Zeid Abdullah,Barakat Assem

Publisher

Elsevier BV

Subject

Inorganic Chemistry,Organic Chemistry,Physical and Theoretical Chemistry,Catalysis

Reference63 articles.

1. Comprehensive Organic Synthesis;Olah,1991

2. Asymmetric Friedel−Crafts Alkylation of Methoxyfuran with Nitroalkenes Catalyzed by Diphenylamine-Tethered Bis(oxazoline)−Zn(II) Complexes

3. Enantioselective Friedel–Crafts alkylation of indoles with nitroalkenes catalyzed by a bis(oxazoline)–Cu(II) complex

4. New Catalytic Approaches in the Stereoselective Friedel–Crafts Alkylation Reaction

5. Asymmetric Friedel-CraftsReactions: Catalytic Enantioselective Addition of Aromatic and HeteroaromaticC-H Bonds to Activated Alkenes, Carbonyl Compounds, andImines

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1. Enantioselective Friedel-Crafts alkylation of 1,3,5-trimethoxybenzene with trans-β-nitrostyrenes catalysed by [Cp*Rh{(R)-Prophos}(H2O)][SbF6]2 (Prophos = propane-1,2-diyl-bis(diphenylphosphane);Journal of Organometallic Chemistry;2024-11

2. Aminocyclopropenium as a New Class of Hydrogen Bonding Catalyst in Friedel–Crafts Alkylation;Catalysts;2023-10-16

3. Catalytic asymmetric Friedel–Crafts alkylation of unprotected indoles with nitroalkenes using a novel chiral Yb(OTf)3–pybox complex;Scientific Reports;2023-09-07

4. Recent Developments in the Synthesis and Anticancer Activity of Indole and Its Derivatives;Current Organic Synthesis;2023-06

5. Friedel–Crafts alkylation of indoles with β-nitroalkenes using ammonium niobium oxalate as a recyclable catalyst;New Journal of Chemistry;2022

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