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Additions of trialkyl phosphites to nitroalkenes

https://doi.org/10.1021/jo00408a027
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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
inferred← citeshttps://doi.org/10.1002/0471264180.or092.02openalex-snapshot
Cyclization of Vinyl and Aryl Azides into Pyrroles, Indoles, Carbazoles, and Related Fused Pyrroles
inferred← citeshttps://doi.org/10.1002/9780470682531.pat0505openalex-snapshot
Phosphorus Derivatives of Hydroxylamines, Oximes and Hydroxamic Acids
inferred← citeshttps://doi.org/10.1002/adts.202500379openalex-snapshot
DFT Study of the Possible Mechanisms for Synthesizing α‐Cyanophosphonates from β‐Nitrostyrenes
inferred← citeshttps://doi.org/10.1002/chin.197902247openalex-snapshot
ChemInform Abstract: ADDITIONS OF TRIALKYL PHOSPHITES TO NITROALKENES
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/hlca.19790620528openalex-snapshot
Dérivés d'énose‐ et d'ynosephosphonates et composés voisins. Communication préliminaire
inferred← citeshttps://doi.org/10.1016/s0957-4166(01)00031-3openalex-snapshot
A practical synthetic approach to chiral α-aryl substituted ethylphosphonates
inferred← citeshttps://doi.org/10.1021/jo900417mopenalex-snapshot
Enantioselective Synthesis of Chiral α-Aryl or α-Alkyl Substituted Ethylphosphonates via Rh-Catalyzed Asymmetric Hydrogenation with a P -Stereogenic BoPhoz-Type Ligand
inferred← citeshttps://doi.org/10.1023/b:rujo.0000003155.15312.f4openalex-snapshot
Hydrophosphorylation of Terminal Alkynes Catalyzed by Palladium
inferred← citeshttps://doi.org/10.1039/c7ob02267kopenalex-snapshot
Pd-Catalysed Suzuki coupling of α-bromoethenylphosphonates with organotrifluoroborates: a general protocol for the synthesis of terminal α-substituted vinylphosphonates
inferred← citeshttps://doi.org/10.1039/d5ob00602copenalex-snapshot
Rhodium-catalyzed enantioselective hydrogenation of (1-arylvinyl)phosphonates with TADDOL-based phosphoramidite P,S ligands
inferred← citeshttps://doi.org/10.1055/a-2239-6819openalex-snapshot
Solvent-Free Synthesis of α-Cyanophosphonates from β-Nitrostyrenes by Using a Deep-Eutectic Solvent Catalyst
inferred← citeshttps://doi.org/10.1080/03086648408077630openalex-snapshot
THE THERMOLYSIS OF PENTA-COORDINATE PHOSPHORUS HETEROCYCLES
inferred← citeshttps://doi.org/10.1080/03086648508074236openalex-snapshot
THE CRYSTAL AND MOLECULAR STRUCTURE OF 2-DIMETHOXYPHOSPHINYL-2-METHOXY-2-PHENYLACETALDEHYDE OXIME. A SINGLE-CRYSTAL X-RAY DIFFRACTION STUDY
inferred← citeshttps://doi.org/10.1134/s1070428026602505openalex-snapshot
Isopropyl Esters of [1-(Het)Arylvinyl]- and [1-(Het)Arylethyl]phosphonic Acids
inferred← citeshttps://doi.org/10.1246/bcsj.53.1625openalex-snapshot
New Synthesis and Hydroboration of Vinylphosphonates
inferred← citeshttps://doi.org/10.2174/138527211795378146openalex-snapshot
β-Hydroxyimino Phosphorus Derivatives. An Efficient Tool in Organic Synthesis
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