## Abstract ChemInform is a weekly Abstracting Service, delivering concise information at a glance that was extracted from about 100 leading journals. To access a ChemInform Abstract of an article which was published elsewhere, please select a βFull Textβ option. The original article is trackable v
Intramolecular Mitsunobu reaction in the regio- and stereoselective synthesis of cis-4,5-disubstituted piperidin-2-ones
β Scribed by Nicole Langlois; Olivier Calvez
- Publisher
- Elsevier Science
- Year
- 2000
- Tongue
- French
- Weight
- 84 KB
- Volume
- 41
- Category
- Article
- ISSN
- 0040-4039
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β¦ Synopsis
Enantiopure cis-4,5-disubstituted piperidin-2-ones were synthesized through the cyclization of O-benzyl hydroxamates under Mitsunobu conditions, followed by samarium diiodide reduction.
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1,4-Bis(arylsulfonyl)-1,2,3,4-tetrahydropyridines in Synthesis. Intramolecular Alkylation Reactions and Stereoselective Synthesis of anti-2,6-Disubstituted Piperidines. -Chiral tetrahydropyridines (I) undergo intramolecular aromatic substitution reactions to give benzofused bicyclic compounds (II)
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