Reaction of benzothiazoline with benzyne - generation of novel heterocyclic sulfur ylide, benzothiazolinium s-ylide
Author:
Publisher
Elsevier BV
Subject
Organic Chemistry,Drug Discovery,Biochemistry
Reference10 articles.
1. Migratory Aptitude of the Ethyl and the Methyl Groups during Stevens Rearrangement of N,N-Dialkyl-2-arylbenzothiazolinium Salts
2. The Structure of Alkylation Products of 2-Substituted 3-Methylbenzolines with Meerwein Reagents
3. A new aspect on alkylation of benzothiazolines.
4. Chemistry of Nitrosoimines. X. Reactions of 3-Substituted 2-Nitrosoimino-2,3,-dihydrobenzothiazoles with Aryl andt-Butyl Grignard Reagents
5. Umsetzungen von Thioäthern mito-Fluor-phenylmagnesiumbromid
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1. An Improved Procedure for Aryne Generation from o‐Triazenylarylboronic Acids through One‐Pot Boronate Formation/Silica Gel Treatment;European Journal of Organic Chemistry;2023-07-13
2. Gram-scale synthesis of the N-phenyl phenothiazine photocatalyst by benzyne addition;Canadian Journal of Chemistry;2022-11-01
3. Silica gel-induced aryne generation from o-triazenylarylboronic acids as stable solid precursors;Organic Chemistry Frontiers;2021
4. Synthesis of Densely Functionalized N-Alkenyl 2-Pyridones via Benzyne-Induced Ring Opening of Thiazolino-Fused 2-Pyridones;Organic Letters;2019-08-16
5. Interception of benzyne with thioethers: a facile access to sulfur ylides under mild conditions;RSC Adv.;2014
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