Reactions of 9-Alkyl-3-aminocarbazoles with Ethyl-3-oxo-butanoate and Identification of the Products Obtained

Sapijanskaitė, Birutė; Mickevicius, Ytautas; Mikulskiene, Gema

doi:10.3390/11010072

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Formation Of Azepino[32-b]carbazoles1

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2019

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“…in mineral oil at 240-250°C, compound 124 could easily be cyclized to 7-ethyl-3-methyl-4,7-dihydro-pyrido[2,3c]-carbazol-1-one (126) (Scheme 44). 62…”

Section: Formation Of Azepino[32-b]carbazolesmentioning

confidence: 99%

Progress in the chemistry of 3-amino-9-ethylcarbazole

Bondock¹,

Alqahtani²,

Fouda³

2019

Turk J Chem

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Generally, 3-amino-9-ethylcarbazole is considered a versatile compound not only for its unique electronic properties but also for its significance as a building block in synthetic, pharmaceutical, and material chemistry. The synthesis, chemical reactivity, and applications of 3-amino-9-ethylcarbazole are described in this review. The presence of the amino group at position 3 exhibits a unique reactivity with both C-2 and C-4. The reactions of 3-amino-9ethylcarbazole are divided into three categories, reactions that involve the amino group and cyclization reactions that involve the amino group and C-2 and/or C-4. In this review, relevant and appropriate applications of the synthesized, isolated, and condensed carbazole derivatives are reported.

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“…in mineral oil at 240-250°C, compound 124 could easily be cyclized to 7-ethyl-3-methyl-4,7-dihydro-pyrido[2,3c]-carbazol-1-one (126) (Scheme 44). 62…”

Section: Formation Of Azepino[32-b]carbazolesmentioning

confidence: 99%