Dimethyl sulfoxide–trimethylsilyl bromide–amine system as a bromonium ion source containing a potential internal nucleophile; unusual bromolactonisation of cyclohex-3-enecarboxylic acid derivatives
Author:
Publisher
Royal Society of Chemistry (RSC)
Link
http://pubs.rsc.org/en/content/articlepdf/1994/P1/P19940000847
Reference35 articles.
1. Novel Bromolactonization Using a Dimethyl Sulfoxide-Trimethylsilyl Bromide-Amine System; Unusual cis-Addition of trans-6-Substituted 3-Cyclohexene-1-carboxylic Acids
2. Regio- and stereo-specific synthesis of cis-(±)-1-acetoxy-4-(acetoxymethyl)cyclopent-2-ene: a key intermediate in the synthesis of carbocyclic nucleosides and pseudo-ribofuranoses
3. Synthesis and synthetic utility of halolactones
4. A new general β-lactone synthesis
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1. A Oxidative Bromination of (Hetero)Arenes in the TMSBr/DMSO System: A Non-Aqueous Procedure Facilitates Synthetic Strategies;ChemistrySelect;2017-01-23
2. ChemInform Abstract: Dimethyl Sulfoxide-Trimethylsilyl Bromide-Amine System as a Bromonium Ion Source Containing a Potential Internal Nucleophile; Unusual Bromolactonization of Cyclohex-3-enecarboxylic Acid Derivatives.;ChemInform;2010-08-19
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4. β-Substituted Cyclohexanecarboxamide: A Nonpeptidic Framework for the Design of Potent Inhibitors of Cathepsin K;Journal of Medicinal Chemistry;2006-01-19
5. Halo- and selenolactonisation: the two major strategies for cyclofunctionalisation;Tetrahedron;2004-06
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