N-Hydroxy indoles as flexible substrates in rearrangements—a novel reaction with activated triple bonds
Author:
Publisher
Elsevier BV
Subject
Organic Chemistry,Drug Discovery,Biochemistry
Reference22 articles.
1. 3,3-Sigmatropic Rearrangements Involving N−O Bond-Cleavage of Enehydroxylamine Derivatives
2. The Hetero-Cope Rearrangement in Organic Synthesis
3. Synthetic applications of -Aryl- -acyl hydroxymic acids. A convenient route to 3-substituted -Benzoyl oxindoles
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1. Mechanistic duality of indolyl 1,3-heteroatom transposition;Chemical Science;2023
2. Further Developments on the Regioselective Synthesis of 3-Aroylindole Derivatives from <i>C</i>-Nitrosoaromatics and Alkynones: A Novel Synthetic Approach to Pravadoline, JWH-073, Indothiazinone Analogues and Related Compounds;International Journal of Organic Chemistry;2022
3. Concise Synthesis of Furo[2,3-b]indolines via [3,3]-Sigmatropic Rearrangement of N-Alkenyloxyindoles;Synlett;2020-08-27
4. Sulfonyl Azoles in the Synthesis of 3-Functionalized Azole Derivatives;The Chemical Record;2016-05-05
5. Rearrangement of N-Oxyenamines and Related Reactions;Chemical Reviews;2014-03-14
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