ChemInform Abstract: FLUORIERTE AZO‐FARBSTOFFE 2. MITT. SYNTH. UND SPEKTROSKOPISCHE EIGENSCHAFTEN VON 2,6‐DIFLUOR‐ UND 2,3,5,6‐TETRAFLUOR‐4‐AMINO‐AZOBENZOLEN UND IHRER N‐METHYL‐ UND 4′‐AETHYL‐DERIVATE

Namkung, Moses J.; Naimy, Norma K.; Cole, C.-A.; Ishikawa, Nobuo; Fletcher, T. Lloyd

doi:10.1002/chin.197026372

Chemischer Informationsdienst. Organische Chemie

1970

DOI: 10.1002/chin.197026372

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ChemInform Abstract: FLUORIERTE AZO‐FARBSTOFFE 2. MITT. SYNTH. UND SPEKTROSKOPISCHE EIGENSCHAFTEN VON 2,6‐DIFLUOR‐ UND 2,3,5,6‐TETRAFLUOR‐4‐AMINO‐AZOBENZOLEN UND IHRER N‐METHYL‐ UND 4′‐AETHYL‐DERIVATE

Moses J. Namkung¹,

Norma K. Naimy²,

C.-A. Cole³

et al.

Abstract: Die Kondensation der geschützten p‐Phenylendiamine (I) mit den Nitrosobenzolen (II) führt zu den Azoverbindungen (III), die zu den freien Aminen (IV) hydrolysiert werden.

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ChemInform Abstract: FLUORIERTE AZO‐FARBSTOFFE 2. MITT. SYNTH. UND SPEKTROSKOPISCHE EIGENSCHAFTEN VON 2,6‐DIFLUOR‐ UND 2,3,5,6‐TETRAFLUOR‐4‐AMINO‐AZOBENZOLEN UND IHRER N‐METHYL‐ UND 4′‐AETHYL‐DERIVATE

Abstract: Die Kondensation der geschützten p‐Phenylendiamine (I) mit den Nitrosobenzolen (II) führt zu den Azoverbindungen (III), die zu den freien Aminen (IV) hydrolysiert werden.

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References 1 publication

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