Umsetzungen von höhermolekularen, konstitutions‐ und molekulareinheitlichen Phenol‐Formaldehyd‐Kondensaten mit 2.4‐Dinitro‐fluorbenzol und Benzoldiazoniumchlorid

6533b824fe1ef96bd127ff32

RESEARCH PRODUCT

Umsetzungen von höhermolekularen, konstitutions‐ und molekulareinheitlichen Phenol‐Formaldehyd‐Kondensaten mit 2.4‐Dinitro‐fluorbenzol und Benzoldiazoniumchlorid

subject

Inorganic Chemistry Chemistry Medicinal chemistry

description

Hohermolekulare, konstitutions- und molekulareinheitliche Phenol-Formaldehyd-Kondensate (Mehrkernverbindungen im Molekulargewichtsbereich von 200 bis 760) mit mehreren Hydroxygruppen konnen mit 2.4-Dinitro-fluorbenzol mit guten Ausbeuten zu Dinitrophenylathern umgesetzt werden. Mehrkernverbindungen, in denen p-Stellungen zu phenolischen Hydroxylen nicht substituiert sind, kuppeln mit Benzoldiazoniumchlorid, ohne das Spaltungen von Methylenbrucken beobachtet wurden.

year	journal	country	edition	language
1961-01-01	Chemische Berichte

https://doi.org/10.1002/cber.19610940135

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