Sydnone Ring as an ortho-Director of Lithiation, 3: One-Pot Regiospecific o-Acylation and Subsequent Sydnone 4-Substitution
Author:
Affiliation:
1. a Chemistry Department , Wright State University , Dayton, Ohio, USA
Publisher
Informa UK Limited
Subject
Organic Chemistry
Link
https://www.tandfonline.com/doi/pdf/10.1080/00397910802664251
Reference7 articles.
1. The sydnone ring as an ortho-director of lithiation. 2.1 Dilithiation of 3-phenylsydnone and regiospecific -aryl acylation using N-methoxy-N-methylamides
2. The sydnone ring as an ortho-director of lithiation. Dilithiation of 3-phenylsydnone and trapping by electrophiles
3. Mesoionic compounds VI. Metallation of sydnones. An estimation of acidity
4. Bromination of sydnones. I. Reaction with 3-arylsydnones containing electron-donors on the aryl ring
5. Approaches to the synthesis of compounds containing fused mesoionic rings
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3. Recent developments in the chemistry of sydnones and sydnone imines;Advances in Heterocyclic Chemistry;2020
4. Heterocycle-Mediated ortho-Functionalization of Aromatic Compounds: The DoM Methodology and Synthetic Utility;Synthesis;2016-04-26
5. Mesoionics;Topics in Heterocyclic Chemistry;2012
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