Z -2-Phenyl-4-[(S)- 2,2-dimethyl-1,3-dioxolan-4-ylmethylen]-5(4H)-oxazolone as the Dienophile in Asymmetric Diels-Alder Reactions
✍ Scribed by Elena Buñuel; Carlos Cativiela; Maria D. Diaz-de-Villegas
- Publisher
- Elsevier Science
- Year
- 1995
- Tongue
- French
- Weight
- 820 KB
- Volume
- 51
- Category
- Article
- ISSN
- 0040-4020
No coin nor oath required. For personal study only.
📜 SIMILAR VOLUMES
1999 stereochemistry stereochemistry (general, optical resolution) O 0030 24 -026 Synthesis of (-)-(4R,5R)-4,5-Bis [di-3'-(2',6'dimethoxypyridyl)phosphinomethyl] -2,2-dimethyl-1,3-dioxolane and Its Application in the Rh-Catalyzed Asymmetric Hydrogenation Reactions. -Asymmetric hydrogenations of a se
Methyl N-(Benzylsulfonyl)oxamate as a Probable Intermediate in the Synthesis of 4-Hydroxy-5-phenyl-3(2H)-isothiazolone 1,1-Dioxide from Phenylmethanesulfamide and Dimethyl Oxalate in the Presence of Bases. -The base-mediated formation of the title isothiazolone dioxide (III) from phenylmethanesulfa