Molecules from Radical Reactions

A special issue of Molbank (ISSN 1422-8599). This special issue belongs to the section "Organic Synthesis".

Deadline for manuscript submissions: closed (31 May 2019) | Viewed by 2217

Special Issue Editor


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Guest Editor
School of Pharmacy, Hyogo Medical University of Health Sciences, 1-3-6 Minatojima, Chuo-ku, Kobe 650-8530, Japan
Interests: organic synthesis and methodology; radical reactions; organocatalysis; asymmetric catalysis; photochemistry; aryne chemistry

Special Issue Information

Dear Colleagues,

Radical reaction has been developed as one of the most powerful methods for constructing carbon–carbon and carbon–heteroatom bonds. Utilizing radical methodologies has advantages over ionic chemistry, for example due the high functional group tolerance and the mild reaction conditions, because neutral radical intermediates are not charged species. Therefore, the use of free radical-mediated reactions in organic synthesis has continued to increase, addressing new strategies for synthesising structurally complex molecules. The focus of this Special Issue is on presenting papers that cover the synthesis of single and new compounds based on radical reactions, electron transfer reactions or photo-induced redox reactions. Short communication papers on this topic are also welcome.

Prof. Dr. Hideto Miyabe
Guest Editor

Manuscript Submission Information

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Keywords

  • radical
  • organic synthesis
  • synthetic etratages
  • electron transfer
  • redox reactions
  • photocatalysis

Published Papers (1 paper)

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Research

5 pages, 511 KiB  
Short Note
2-(3,4-Dimethoxyphenyl)-N-(4-methoxyphenyl)-1-propyl-1H-benzo[d]imidazole-5-carboxamide
by Prakash Bhaskar, Vasantha Kumar, Suresha Kumara Tholappanavara Hanumanthappa and Sowmya Haliwana Banakara Vijaykumar
Molbank 2019, 2019(3), M1079; https://doi.org/10.3390/M1079 - 09 Sep 2019
Cited by 1 | Viewed by 1945
Abstract
2-(3,4-Dimethoxyphenyl)-N-(4-methoxyphenyl)-1-propyl-1H-benzo[d]imidazole-5-carboxamide was synthesized by the ‘one-pot’ reductive cyclization of N-(4-methoxyphenyl)-3-nitro-4-(propylamino)benzamide with 3,4-dimethoxybenzaldehyde, using sodium dithionite as a reductive cyclizing agent using DMSO as a solvent. The structure of newly synthesized compound was elucidated based on IR, 1H-NMR, 13C-NMR, and LC-MS data. Full article
(This article belongs to the Special Issue Molecules from Radical Reactions)
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Scheme 1

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