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References from Molecular Iodine-Catalyzed Selective C-3 Benzylation of Indoles with Benzylic Alcohols: A Greener Approach toward Benzylated Indoles. Local targets link to admitted publications; unresolved targets remain external evidence.
Bioactive Indole Alkaloids and Phenyl Ether Derivatives from a Marine-Derived Aspergillus sp. Fungus
10.1021/np300707x · 2013 · External reference
Indole-based fibrates as potential hypolipidemic and antiobesity agents
10.1021/jm201697v · 2012 · External reference
Indoles in Multicomponent Processes (MCPs)
10.1021/cr2003954 · 2012 · External reference
Mushroom-derived indole alkaloids
10.1021/acs.jnatprod.7b00390 · 2017 · External reference
A review of new developments in the Friedel–Crafts alkylation – From green chemistry to asymmetric catalysis
10.3762/bjoc.6.6 · 2010 · External reference
Catalytic enantioselective Friedel–Crafts alkylation of indoles with nitroalkenes by using a simple thiourea organocatalyst
10.1002/ange.200500227 · 2005 · External reference
10.1002/9783527626977
10.1002/9783527626977 · 2009 · External reference
Electrophilic allylations and benzylations of indoles in neutral aqueous or alcoholic solutions
10.1021/ol0618555 · 2006 · External reference
Au(III)/TPPMS-catalyzed benzylation of indoles with benzylic alcohols in water
10.1021/jo402151g · 2013 · External reference
In(OTf)3 catalyzed C3-benzylation of indoles with benzyl alcohols in water
10.1039/c3ra40251g · 2013 · External reference
Iron-Catalyzed Direct C3-Benzylation of Indoles with Benzyl Alcohols through Borrowing Hydrogen
10.1021/acs.joc.7b01603 · 2017 · External reference
An FeCl3-catalyzed highly C3-selective Friedel–Crafts alkylation of indoles with alcohols
10.1016/j.tetlet.2007.07.208 · 2007 · External reference
Catalytic C-Alkylation of Pyrroles with Primary Alcohols: Hans Fischer’s Alkali and a New Method with Iridium P, N, P-Pincer Complexes
10.1002/ejoc.201800146 · 2018 · External reference
Palladium (II)-Catalyzed Efficient C-3 Functionalization of Indoles with Benzylic and Allylic Alcohols under Co-Catalyst, Acid, Base, Additive and External Ligand-Free Conditions
10.1002/adsc.201300048 · 2013 · External reference
General and Selective C-3 Alkylation of Indoles with Primary Alcohols by a Reusable Pt Nanocluster Catalyst
10.1002/chem.201302464 · 2013 · External reference
Selective Ruthenium-Catalyzed N-Alkylation of Indoles by Using Alcohols
10.1002/chem.200903144 · 2010 · External reference
Photoredox Catalysis Induced Bisindolylation of Ethers/Alcohols via Sequential C–H and C–O Bond Cleavage
10.1021/acs.orglett.7b03073 · 2017 · External reference
Metal-Free Synthesis of Pharmaceutically Important Biaryls by Photosplicing
10.1002/anie.201805961 · 2018 · External reference
Environmentally friendly and regioselective C3-alkylation of indoles with alcohols through a hydrogen autotransfer strategy
10.1016/j.tetlet.2013.04.062 · 2013 · External reference
Br2-Catalyzed regioselective dehydrative coupling of indoles with acyloins: direct synthesis of α-(3-indolyl) ketones
10.1039/c6ra03321k · 2016 · External reference
A highly regioselective C-3 benzylation reaction of indoles with alcohols catalysed by an N-heterocyclic carbene
10.3184/174751915x14376593652711 · 2015 · External reference
Direct benzylation and allylic alkylation in high-temperature water without added catalysts
10.1016/j.tetlet.2010.01.112 · 2010 · External reference
Recent advances in the direct nucleophilic substitution of allylic alcohols through SN1-type reactions
10.1055/s-0033-1340316 · 2014 · External reference
Organocatalyzed Friedel–Crafts arylation of benzylic alcohols
10.1016/j.tetlet.2010.02.151 · 2010 · External reference
Brønsted acid catalyzed C3-selective propargylation and benzylation of indoles with tertiary alcohols
10.1055/s-2008-1072584 · 2008 · External reference
Nucleophilic substitution reactions of alcohols with use of montmorillonite catalysts as solid Brønsted acids
10.1021/jo070416w · 2007 · External reference
Direct substitution of alcohols in pure water by brønsted acid catalysis
10.3390/molecules22040574 · 2017 · External reference
Reaction mechanism of iodine-catalyzed michael additions
10.1021/acs.joc.7b00445 · 2017 · External reference
Mechanisms in Iodine Catalysis
10.1002/chem.201706136 · 2018 · External reference
Iodine-catalyzed regioselective 2-sulfonylation of indoles with sodium sulfinates
10.1021/ol402987u · 2014 · External reference
Metal-free, iodine-catalyzed regioselective sulfenylation of indoles with thiols
10.1016/j.tetlet.2016.03.073 · 2016 · External reference
Iodine-catalyzed nucleophilic substitution reactions of benzylic alcohols
10.1055/s-2008-1072652 · 2008 · External reference
Molecular iodine as a mild catalyst for cross-coupling of alkenes and alcohols
10.1515/pac-2017-0414 · 2018 · External reference
Iodine catalysis: A green alternative to transition metals in organic chemistry and technology
10.1016/j.reffit.2015.06.001 · 2015 · External reference
Iodine-catalyzed cascade formal [3+ 3] cycloaddition reaction of indolyl alcohol derivatives with enaminones: constructions of functionalized spirodihydrocarbolines
10.1021/cs400703u · 2013 · External reference
Polyhalogen Complex Ions
1967 · External reference
