Quinonic enaminones; synthesis of new dialkylaminovinyl and bis(dialkylaminovinyl) derivatives of quinones

Mohammad Alnabari; Shmuel Bittner

doi:10.1055/s-2000-6314

Quinonic enaminones; synthesis of new dialkylaminovinyl and bis(dialkylaminovinyl) derivatives of quinones

Mohammad Alnabari, Shmuel Bittner

Department of Chemistry

Research output: Contribution to journal › Article › peer-review

12 Scopus citations

Abstract

The reaction of halogenated quinones with a variety of secondary amines in the presence of acetaldehyde proceeds via intermediate formation of enamines and produces mono quinonic enaminones. The use of two equivalents of enamine results in both symmetrical and nonsymmetrical bis-derivatives.

Original language	English
Pages (from-to)	1087-1090
Number of pages	4
Journal	Synthesis
Issue number	8
DOIs	https://doi.org/10.1055/s-2000-6314
State	Published - 1 Jan 2000

Keywords

Enamines
Quinones
Quinonic enaminones

ASJC Scopus subject areas

Catalysis
Organic Chemistry

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10.1055/s-2000-6314

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title = "Quinonic enaminones; synthesis of new dialkylaminovinyl and bis(dialkylaminovinyl) derivatives of quinones",

abstract = "The reaction of halogenated quinones with a variety of secondary amines in the presence of acetaldehyde proceeds via intermediate formation of enamines and produces mono quinonic enaminones. The use of two equivalents of enamine results in both symmetrical and nonsymmetrical bis-derivatives.",

keywords = "Enamines, Quinones, Quinonic enaminones",

author = "Mohammad Alnabari and Shmuel Bittner",

year = "2000",

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doi = "10.1055/s-2000-6314",

language = "English",

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journal = "Synthesis",

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T1 - Quinonic enaminones; synthesis of new dialkylaminovinyl and bis(dialkylaminovinyl) derivatives of quinones

AU - Alnabari, Mohammad

AU - Bittner, Shmuel

PY - 2000/1/1

Y1 - 2000/1/1

N2 - The reaction of halogenated quinones with a variety of secondary amines in the presence of acetaldehyde proceeds via intermediate formation of enamines and produces mono quinonic enaminones. The use of two equivalents of enamine results in both symmetrical and nonsymmetrical bis-derivatives.

AB - The reaction of halogenated quinones with a variety of secondary amines in the presence of acetaldehyde proceeds via intermediate formation of enamines and produces mono quinonic enaminones. The use of two equivalents of enamine results in both symmetrical and nonsymmetrical bis-derivatives.

KW - Enamines

KW - Quinones

KW - Quinonic enaminones

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U2 - 10.1055/s-2000-6314

DO - 10.1055/s-2000-6314

M3 - Article

AN - SCOPUS:0033911332

SN - 0039-7881

SP - 1087

EP - 1090

JO - Synthesis

JF - Synthesis

IS - 8

ER -

Quinonic enaminones; synthesis of new dialkylaminovinyl and bis(dialkylaminovinyl) derivatives of quinones

Abstract

Keywords

ASJC Scopus subject areas

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