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A new methodology for synthesis of a chiral phosphinocarboxylic acid through Michael cyclization-aldol tandem reaction of chiral alpha,beta,chi,psi-unsaturated bisphosphine oxide and application in palladium-catalyzed asymmetric allylic alkylation
- Source :
- Journal of Organic Chemistry. August 9, 2002, Vol. 67 Issue 16, p5864, 4 p.
- Publication Year :
- 2002
-
Abstract
- Research has been conducted on the chiral alpha,beta,psi,omega-unsaturated bisphosphine oxide. Results indicate that after the treatment with lithium diisopropylamide and benzaldehyde this compound underwent Michael cyclization-aldol tandem reaction in producing endo-alpha,beta-unsaturated bisphosphine oxides.
- Subjects :
- Chemistry, Organic -- Research
Ring formation (Chemistry) -- Physiological aspects
Carboxylic acids -- Physiological aspects
Phosphorus -- Physiological aspects
Chemical reactions -- Analysis
Oxides -- Physiological aspects
Palladium catalysts -- Physiological aspects
Alkylation -- Physiological aspects
Lithium -- Physiological aspects
Chirality -- Physiological aspects
Amides -- Physiological aspects
Biological sciences
Chemistry
Subjects
Details
- ISSN :
- 00223263
- Volume :
- 67
- Issue :
- 16
- Database :
- Gale General OneFile
- Journal :
- Journal of Organic Chemistry
- Publication Type :
- Academic Journal
- Accession number :
- edsgcl.90903149