The sydnone ring as an ortho-director of lithiation. 2.1 Dilithiation of 3-phenylsydnone and regiospecific -aryl acylation using N-methoxy-N-methylamides
Author:
Publisher
Elsevier BV
Subject
Organic Chemistry,Drug Discovery,Biochemistry
Reference16 articles.
1. The sydnone ring as an ortho-director of lithiation. Dilithiation of 3-phenylsydnone and trapping by electrophiles
2. Mesoionic compounds VI. Metallation of sydnones. An estimation of acidity
3. Bromination of sydnones. I. Reaction with 3-arylsydnones containing electron-donors on the aryl ring
4. Bromination of sydnones. II Bromination of 3-(2-aminophenyl)sydnone and related compounds
5. Debromination of 3-Aryl-4-bromosydnones with Sodium Borohydride
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1. Sydnone: Synthesis, Reactivity and Biological Activities;Current Medicinal Chemistry;2023-03
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3. Synthesis of acylnaphthylamines and their applications in the formation of benzoquinazolines;Arkivoc;2018-10-13
4. 3-(4-Chlorophenyl)-4-phenylthiosydnone;IUCrData;2016-10-14
5. Improved Method for the Iodination of Sydnones;Synthetic Communications;2013-09-04
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