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Addition, substitution and deoxygenation reactions of .alpha.-phenyl-.beta.-nitrostyrenes with the anions of thiols and diethyl phosphite: formation of indoles by reaction with ethyl phosphites
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inferred← citeshttps://doi.org/10.2139/ssrn.4758293openalex-extracted
Dft Study of the Possible Mechanisms for the Synthesis of Α-Cyanophosphonates from Β-Nitrostyrenes
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Cyclization of Vinyl and Aryl Azides into Pyrroles, Indoles, Carbazoles, and Related Fused Pyrroles
inferred← citeshttps://doi.org/10.1002/0471264180.or111.02openalex-snapshot
Reductive Cyclization of 2‐Nitro‐ and β‐Nitrostyrenes, 2‐Nitrobiphenyls, and 1‐Nitro‐1,3‐Dienes to Indoles, Carbazoles, and Pyrroles
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The Synthesis of Functionalized Phosphinic and Phosphonic Acids and their Derivatives. Part B : Diazo, Nitro and Amino Functionalized Acids
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Phosphorus Derivatives of Hydroxylamines, Oximes and Hydroxamic Acids
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Cadogan–Sundberg Indole Synthesis
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DFT Study of the Possible Mechanisms for Synthesizing α‐Cyanophosphonates from β‐Nitrostyrenes
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Solvent‐Controlled Copper‐Catalyzed Radical Decarboxylative Coupling for Alkenyl C(sp2)−P Bond Formation
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ChemInform Abstract: Addition, Substitution, and Deoxygenation Reactions of α‐Phenyl‐. beta.‐nitrostyrenes with the Anions of Thiols and Diethyl Phosphite: Formation of Indoles by Reaction with Ethyl Phosphites.
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Synthesis of Indoles by Palladium‐Catalyzed Reductive Cyclization of β‐Nitrostyrenes with Carbon Monoxide as the Reductant
inferred← citeshttps://doi.org/10.1002/ejoc.201900144openalex-snapshot
Ceric(IV) Ammonium Nitrate Mediated Phosphorylation of Alkenes: Easy Access to (E)‐Vinylphosphonates
inferred← citeshttps://doi.org/10.1002/hc.520030303openalex-snapshot
Reactions of β‐nitrostyrenes with tert‐butylmercury halides in the presence of lodide lon
inferred← citeshttps://doi.org/10.1002/hc.520030512openalex-snapshot
Studies on organophosphorus compounds 56. New reaction of dialkyl phosphites with 2‐nitrostyrene derivatives—a facile route to N‐hydroxy‐3‐indole phosphonates and indol‐2‐one phosponates
inferred← citeshttps://doi.org/10.1002/poc.610060110openalex-snapshot
α‐Versus β‐carbon nucleophilic attack in vinylic substitution
inferred← citeshttps://doi.org/10.1016/b978-0-12-819962-6.00002-6openalex-snapshot
Synthesis and Reactions of Nitroindoles
inferred← citeshttps://doi.org/10.1016/b978-0-443-13583-5.00008-6openalex-snapshot
Synthesis of azirines
inferred← citeshttps://doi.org/10.1016/b978-044452737-0/50004-1openalex-snapshot
Reactivity of H-Phosphonates
inferred← citeshttps://doi.org/10.1016/j.tet.2004.08.086openalex-snapshot
The nitration of some 4,6-dimethoxyindoles
inferred← citeshttps://doi.org/10.1016/j.tet.2008.11.034openalex-snapshot
Indole synthesis: palladium-catalyzed C–H bond amination via reduction of nitroalkenes with carbon monoxide
inferred← citeshttps://doi.org/10.1016/j.tet.2011.06.040openalex-snapshot
Indole synthesis: a review and proposed classification
inferred← citeshttps://doi.org/10.1016/j.tetlet.2007.01.173openalex-snapshot
Direct palladium-catalyzed C-3 arylation of indoles
inferred← citeshttps://doi.org/10.1016/j.tetlet.2013.07.157openalex-snapshot
Mild, efficient Fischer indole synthesis using 2,4,6-trichloro-1,3,5-triazine (TCT)
inferred← citeshttps://doi.org/10.1016/s0040-4039(97)01272-0openalex-snapshot
Synthesis of 2-nitroindoles via the Sundberg indole synthesis
inferred← citeshttps://doi.org/10.1021/cr030451copenalex-snapshot
Synthetic Methods for Azaheterocyclic Phosphonates and Their Biological Activity
inferred← citeshttps://doi.org/10.1021/jo9803277openalex-snapshot
Synthesis of 2,3-Disubstituted Indoles via Palladium-Catalyzed Annulation of Internal Alkynes
inferred← citeshttps://doi.org/10.1021/ol9006663openalex-snapshot
Simple Conversion of Enamines to 2 H -Azirines and Their Rearrangements under Thermal Conditions
inferred← citeshttps://doi.org/10.1039/c3sc50773dopenalex-snapshot
Synthesis of nitrodienes, nitrostyrenes, and nitrobiaryls through palladium-catalyzed couplings of β-nitrovinyl and o-nitroaryl thioethers
inferred← citeshttps://doi.org/10.1039/c5cc04826eopenalex-snapshot
Stereoselective synthesis of vinylphosphonates and phosphine oxides via silver-catalyzed phosphorylation of styrenes
inferred← citeshttps://doi.org/10.1039/c6ra19002bopenalex-snapshot
Silver-catalyzed synthesis of 2-arylvinylphosphonates by cross-coupling of β-nitrostyrenes with H-phosphites
inferred← citeshttps://doi.org/10.1039/c6ra21144eopenalex-snapshot
Synthesis of 3-arylindole derivatives from nitroalkane precursors
inferred← citeshttps://doi.org/10.1039/c7ra06464kopenalex-snapshot
Mono and double Mizoroki–Heck reaction of aryl halides with dialkyl vinylphosphonates using a reusable palladium catalyst under aqueous medium
inferred← citeshttps://doi.org/10.1039/co9940100145openalex-snapshot
Recent developments in indole ring synthesis—methodology and applications
inferred← citeshttps://doi.org/10.1055/b-0035-128263openalex-snapshot
10.13 Product Class 13: Indole and Its Derivatives
inferred← citeshttps://doi.org/10.1080/01961779508048739openalex-snapshot
Polyhalovinyl Sulfones as Polyfunctional Electrophilic Substrates in Reactions with Nucleophiles
inferred← citeshttps://doi.org/10.21203/rs.3.rs-3737180/v1openalex-snapshot
DFT study of the possible mechanisms for the synthesis of α-cyanophosphonates from β- nitrostyrenes
inferred← citeshttps://doi.org/10.2174/138527210793358277openalex-snapshot
Synthesis of Indole Derivatives with Biological Activity by Reactions Between Unsaturated Hydrocarbons and N-Aromatic Precursors
inferred← citeshttps://doi.org/10.6023/cjoc202307030openalex-snapshot
Regioselective Synthesis of β-Silyl-Substituted Vinylphosphine Oxides via Copper-Catalyzed Protosilylation of Dialkynylphosphine Oxides
inferred← citeshttps://doi.org/10.6060/tcct.2017604.5560openalex-snapshot
SYNTHESIS OF N-HYDROXYINDOLES
inferred← citeshttps://doi.org/10.70675/b2f2c21eza095z4cedzb618z7e1d9f61a8c4openalex-snapshot
Ciblage d'enzymes du métabolisme purique chez Plasmodium falciparum : Conception et étude de molécules bioactives
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