@article{c646e9b172ea45b287b66771ef354b88,
title = "Synthesis of 2-monosubstituted indolin-3-ones by cine-substitution of 3-azido-2-methoxyindolines",
abstract = "We report herein a formal cine-substitution/hydrolysis of 3-azidoindoles generated from 3-azido-2-methoxyindolines (AZINs). This protocol enables the introduction of various carboxylic acids and alcohols into indolin-3-ones at the C2-position, affording 2-monoacyloxy or alkoxy indolin-3-ones.",
author = "Toshiki Yamashiro and Takumi Abe and Daisuke Sawada",
note = "Funding Information: This work was partly supported by the Grants-in-Aid for KAKENHI S (17H06173) from the Ministry of Education, Culture, Sports, Sciences and Technology (MEXT) of the Japan Society for the Promotion of Sciences (JSPS). T. Y. thanks the Nagai Memorial Research Scholarship from the Pharmaceutical Society of Japan. Publisher Copyright: {\textcopyright} 2022 The Royal Society of Chemistry",
year = "2022",
month = feb,
day = "8",
doi = "10.1039/d2qo00048b",
language = "English",
volume = "9",
pages = "1897--1903",
journal = "Organic Chemistry Frontiers",
issn = "2052-4110",
publisher = "Royal Society of Chemistry",
number = "7",
}