1974
DOI: 10.1002/chin.197452356
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ChemInform Abstract: SYNTHESE UND EIGENSCHAFTEN DER AETHYL‐O‐TOLYL‐O‐, M‐ UND P‐AMINOPHENYLARSINE

Abstract: o‐Tolylarsonsäure (I) wird zum o‐Tolyldichlorarsin (II) reduziert und mit Hilfe von Bleitetraäthyl in das o‐Tolyläthylchlorarsin (III) übergeführt.

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“…The Grignard reagent is the organometallic compound most widely employed in these syntheses (39). Organolithium (40), organoaluminum (41), organotin (42), organocadmium (43), and organomercury (44) compounds have also been employed. Some triarylarsines (Ar 3 As) can be prepared by the sodium-promoted interaction of an aryl halide and an arsenic trihalide (AsX 3 ) (45): This type of reaction is sometimes considered a variant of the Wurtz-Fittig reaction.…”
Section: Tertiarymentioning
confidence: 99%
“…The Grignard reagent is the organometallic compound most widely employed in these syntheses (39). Organolithium (40), organoaluminum (41), organotin (42), organocadmium (43), and organomercury (44) compounds have also been employed. Some triarylarsines (Ar 3 As) can be prepared by the sodium-promoted interaction of an aryl halide and an arsenic trihalide (AsX 3 ) (45): This type of reaction is sometimes considered a variant of the Wurtz-Fittig reaction.…”
Section: Tertiarymentioning
confidence: 99%