Reactions of primary amines with epoxides

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Assessing the Potential for the Reactions of Epoxides with Amines on Secondary Organic Aerosol Particles.

Nuclear magnetic resonance techniques were used to study the kinetics and products of the reaction of a variety of epoxides with various amines under varying pH conditions. In agreement with a previous finding, the amine-epoxide reactions were found to be water-catalyzed and not directly dependent on the pH of the reaction environment. At pH values higher than the pK(a) of the particular amine,...

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Microwave Irradiation Promoted Reactions of Benzoxazin-4-Ones with Primary Amines. Preparation of 4(2=3H)-Quinazolinones

An efficient synthesis of 3-substituted or 2,3-disubstituted 4(3H)-quinazolinones from benzoxazin-4-ones and primary amines under microwave irradiation in unsealed vessels is described.

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Variations in product in reactions of naphthoquinone with primary amines

Reaction of 1,2-naphthoquinone with primary amines gives a 2-amino-1,4-naphthoquinone derivative which is equivalent to 1,2 to 1,4 carbonyl transposition. For example the reaction of 1,2-naphthoquinone with 4-methoxyaniline gives 2-(4-methoxyanilino)-naphthoquinone-1,4-(4-methoxyanil) (1) and with n-butylamine gives 2-(butylamino)-naphthoquinone-1,4-butylimine (2) respectively. The compounds 1 ...

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Cu-catalyzed cross-coupling reactions of epoxides with organoboron compounds.

A copper-catalyzed cross-coupling reaction of epoxides with arylboronates is described. This reaction is not limited to aromatic epoxides, because aliphatic epoxides are also suitable substrates. In addition, N-sulfonyl aziridines can be successfully converted into the products. This reaction provides convenient access to β-phenethyl alcohols, which are valuable synthetic intermediates.

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microwave irradiation promoted reactions of benzoxazin-4-ones with primary amines. preparation of 4(2=3h)-quinazolinones

an efficient synthesis of 3-substituted or 2,3-disubstituted 4(3h)-quinazolinones from benzoxazin-4-ones and primary amines under microwave irradiation in unsealed vessels is described.

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ژورنال

عنوان ژورنال: Journal of Applied Polymer Science

سال: 1962

ISSN: 0021-8995,1097-4628

DOI: 10.1002/app.1962.070062431