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Asymmetric synthesis of ring functionalized trans-2,6-disubstituted piperidines from N-sulfinyl [delta]-amino [beta]-keto phosphonates. Total synthesis of (-)-myrtine
- Source :
- Journal of Organic Chemistry. March 16, 2007, Vol. 72 Issue 6, p2046, 7 p.
- Publication Year :
- 2007
-
Abstract
- Asymmetric synthesis of ring functionalized trans-2,6-disubstituted piperidines from N-sulfinyl [delta]-amino [beta]-keto phosphonates was carried out. The method involves the one-pot conversion of sulfinimine-derived N-sulfinyl [delta]-amino [beta]-ketophosphonates, the stereoselective addition of organocuprates and one the one-pot dephosphorylation of the 3-phosphoryl piperidiens.
- Subjects :
- Heterocyclic aromatic compounds -- Chemical properties
Heterocyclic aromatic compounds -- Structure
Phosphonates -- Chemical properties
Phosphonates -- Structure
Organosulfur compounds -- Structure
Organosulfur compounds -- Chemical properties
Amino compounds -- Chemical properties
Biological sciences
Chemistry
Subjects
Details
- Language :
- English
- ISSN :
- 00223263
- Volume :
- 72
- Issue :
- 6
- Database :
- Gale General OneFile
- Journal :
- Journal of Organic Chemistry
- Publication Type :
- Academic Journal
- Accession number :
- edsgcl.165420519