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Addition of trimethyl phosphite to .beta.-nitrostyrene

https://doi.org/10.1021/jo00963a027
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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.or036.02openalex-snapshot
Phosphorus Addition at sp 2Carbon
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.197410385openalex-snapshot
ChemInform Abstract: ADDITION OF TRIMETHYL PHOSPHITE TO BETA‐NITROSTYRENE
inferred← citeshttps://doi.org/10.1007/bf00973418openalex-snapshot
Hydrogen bonds and structure of phosphorus-containing oximes
inferred← citeshttps://doi.org/10.1016/s0040-4039(01)83102-6openalex-snapshot
Ungewohnliche p-funktionalisierung von β-nitrostyrolen
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/10.1080/03086648508074236openalex-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/10.1201/9780203998243.ch3openalex-snapshot
C–P bond formation using nucleophilic trivalent phosphorus reagents
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
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