Front Cover: Recent Advances for Synthesis of Benzothiazoles from Arylmethylamines (Asian J. Org. Chem. 1/2025)

IF 2.8 4区 化学 Q1 CHEMISTRY, ORGANIC Asian Journal of Organic Chemistry Pub Date : 2025-01-17 DOI:10.1002/ajoc.202580101
Vikas D. Kadu
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Abstract

The development towards C(sp3)-H functionalization of arylmethylamines has been the main attraction for synthetic organic chemists.In article number e202400427 by Vikas D. Kadu, the synthetic approaches from C-H/C-N bond functionalization of arylmethylamines/amines as a new emerging substrate are described in detail towards the synthesis of substituted benzothiazoles with insights into substrate scope and the reaction mechanistic pathway for the formation of final targeted products.

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来源期刊
CiteScore
4.70
自引率
3.70%
发文量
372
期刊介绍: Organic chemistry is the fundamental science that stands at the heart of chemistry, biology, and materials science. Research in these areas is vigorous and truly international, with three major regions making almost equal contributions: America, Europe and Asia. Asia now has its own top international organic chemistry journal—the Asian Journal of Organic Chemistry (AsianJOC) The AsianJOC is designed to be a top-ranked international research journal and publishes primary research as well as critical secondary information from authors across the world. The journal covers organic chemistry in its entirety. Authors and readers come from academia, the chemical industry, and government laboratories.
期刊最新文献
Front Cover: Recent Advances for Synthesis of Benzothiazoles from Arylmethylamines (Asian J. Org. Chem. 1/2025) One‐Pot Synthesis of 2‐Substituted Indoles and 7‐Azaindoles via Sequential Alkynylation and Cyclization of 2‐Iodo‐N‐mesylarylamines and Alkynes in the Presence of Cu2O Ring Expansion from 16‐Membered Macrocyclic Lactones Using Yamaguchi and Photoinduced Decarboxylative Radical Macrolactonization Ru(II)‐catalyzed ortho C−H Arylation of Heterocyclic Biaryls In Situ Generated 1‐Naphthylmethyl Radicals from Bis(1‐Naphthylmethyl)tin Dichlorides: Utilization for C−C, C−N, and C−O Bond‐Forming Reactions
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