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A Study of Minisci Reaction by Changing Fe2+ Equivalency: Preparation of Arylpyridinyl Methanol

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Date

2019

Journal Title

Journal ISSN

Volume Title

Publisher

ACG Publications

Open Access Color

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Abstract

We aimed the synthesis of carboxamide 8 and 10, however, beside the main product, one more species was detected in the reaction solution. The characterization of this side product showed that it was the other isomer of the main product. To establish reaction conditions for the synthesis of carboxamide derivatives, we have set up several experiments by changing the Fe2+ stoichiometry. When a molar equivalent Fe2+ was used, only two reaction products 8 and 10 were obtained. The increase in Fe2+ stoichiometry caused the formation of side product 9 and 11 even formation of reduced alcohol products (12-15) by Minisci reaction.

Description

Ozgeris, Bunyamin/0000-0002-3783-6501

Keywords

Minisci Reaction, Nicotinamide, Isonicotinamide, Diarylmethanol

Fields of Science

Citation

WoS Q

Q3

Scopus Q

Q3

Source

Organic Communications

Volume

12

Issue

3

Start Page

143

End Page

148
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