1,4-Bis(arylsulfonyl)-1,2,3,4-tetrahydropyridines in synthesis. Regio- and stereoselective SN1 reactions
Author:
Publisher
Elsevier BV
Subject
Organic Chemistry,Drug Discovery,Biochemistry
Reference15 articles.
1. 1,4-Bis(arylsulfonyl)-1,2,3,4-tetrahydropyridines in Synthesis. Highly Regio- and Stereoselective SN1′ and Alkylation Reactions
2. 1,4-Bis(arylsulfonyl)-1,2,3,4-tetrahydropyridines in Synthesis. Intramolecular Alkylation Reactions and Stereoselective Synthesis of Anti-2,6-Disubstituted Piperidines
3. Synthesis and chemistry of 5,6-dihydropyridinium salt adducts. Synthons for general electrophilic and nucleophilic substitution of the piperidine ring system
4. Novel applications of the modified polonovski reaction - V1 silyl enolates as nucleophilic alkylating reagents
5. Short synthesis of (±)-hirsutine: Direct addition of dimethyl malonate anion to a 1,4-conjugate iminium salt of appropriate 3-ethylindolo[2,3-a]quinolizidine
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1. 5-Methylene N-acyl dihydropyridazinium ions as novel Mannich-type acceptors in 1,4 additions of nucleophiles;Organic Chemistry Frontiers;2018
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3. ChemInform Abstract: 1,4-Bis(arylsulfonyl)-1,2,3,4-tetrahydropyridines in Synthesis. Regio- and Stereoselective SN1 Reactions.;ChemInform;2010-05-22
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