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Current Organic Chemistry

Editor-in-Chief

ISSN (Print): 1385-2728
ISSN (Online): 1875-5348

Editorial

Recent Topics in Organohalogen Reagents and Compounds

Author(s): Toshifumi Dohi*

Volume 24, Issue 18, 2020

Page: [2029 - 2030] Pages: 2

DOI: 10.2174/138527282418201106141610

Abstract

This Special Issue covers the hot topics on recent synthetic interest in halogen and related chemistry as well as the unique characteristics of halogen compounds. The excellent reviews by the experts and eminent researchers engaged in the recent advances, i.e., preparations, reactions, and mechanistic studies of unique organohalogen compounds, halogen bond interaction as the catalysis, and halogen-controlled unique reactions for synthesizing useful organic molecules, such as pharmaceutical compounds and organic materials, are provided in this Special Issue.

Keywords: Organohalogen compounds, halonium and related intermediates, hypervalent iodine compounds, halogen-bonding, halogenation, halogenating agents, synthetic application.

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[1]
Kumar, R.; Sharma, N.; Prakash, O. Hypervalent iodine reagents in the synthesis of flavonoids and related compounds. Curr. Org. Chem., 2020, 24(18), 2031-2047.
[http://dx.doi.org/10.2174/1385272824999200420074551]
[2]
Saito, A. Hypervalent iodine-mediated/catalyzed oxidative cycloisomerization/annulation of alkynes for metal-free synthesis of oxazoles. Curr. Org. Chem., 2020, 24(18), 2048-2069.
[http://dx.doi.org/10.2174/1385272824999200510232438]
[3]
Wang, Y.; An, G.; Wang, L.; Han, J.W. Diaryliodonium salts: structures and synthesis. Curr. Org. Chem., 2020, 24(18), 2070-2105.
[http://dx.doi.org/10.2174/1385272824999200507124328]
[4]
Zheng, H.; Xue, X-S. Recent computational studies on the mechanism of hypervalent iodine mediated dearomatization of phenols. Curr. Org. Chem., 2020, 24(18), 2106-2117.
[http://dx.doi.org/10.2174/1385272824999200620223218]
[5]
Yamada, S.; Konno, S. Recent advances in halogen bond-assisted organic synthesis. Curr. Org. Chem., 2020, 24(18), 2118-2152.
[http://dx.doi.org/10.2174/1385272823666191209112543]
[6]
Yamamoto, Y.; Kawaguchi, S.; Kodama, S.; Nomoto, A.; Ogawa, A. Highly selective hydroiodination of carbon–carbon double or triple bonds. Curr. Org. Chem., 2020, 24(18), 2153-2168.
[http://dx.doi.org/10.2174/1385272824666191227111257]
[7]
Tarui, A.; Karuo, Y.; Sato, K.; Kawai, K.; Omote, M. Stereoselective synthesis of multisubstituted α-fluoro-β-lactams. Curr. Org. Chem., 2020, 24(18), 2169-2180.
[http://dx.doi.org/10.2174/1385272824666200221114707]
[8]
Wang, L.; Li, Z.; Liu, J.; Han, J.; Moriwaki, H.; Soloshonok, V.A. Recent developments in the asymmetric detrifluoroacetylative reactions of in situ generated mono-fluorinated enolates. Curr. Org. Chem., 2020, 24(18), 2181-2191.
[http://dx.doi.org/10.2174/1385272824999200801022712]

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