Indoline hemiaminals: a platform for accessing anthranilic acid derivatives through oxidative deformylation
Author:
Affiliation:
1. Graduate School of Medicine, Dentistry and Pharmaceutical Sciences, Okayama University, 1-1-1 Tsushima-naka, Kita-ku, Okayama 7008530, Japan
2. School of Pharmacy, Shujitsu University, 1-6-1, Nishigawara, Naka-ku, Okayama, 7038516, Japan
Abstract
Funder
Japan Society for the Promotion of Science
Japan Science and Technology Corporation
Publisher
Royal Society of Chemistry (RSC)
Link
http://pubs.rsc.org/en/content/articlepdf/2024/OB/D4OB01218F
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1. Design, Synthesis, and Cytotoxic Activity of Novel Natural Arylsulfonamide-Inspired Molecules
2. Sargassulfamide A, an Unprecedented Amide Derivative from the Seaweed Sargassum naozhouense
3. First discovery of sulfonamides derivatives with acetylcholinesterase inhibitory activity in fungus Pestalotiopsis sp. HNY36-1D
4. The reactions of oxindoles and isatin with nitrobenzyl chlorides
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