Stereoselective Synthesis of MeBmt and Methyl (4 R ,5 S )-5-Isopropyl-2- phenyloxazoline-4-carboxylate by a Pd-Catalyzed Equilibration
โ Scribed by Cook, Gregory R.; Shanker, P. Sathya
- Book ID
- 125943653
- Publisher
- American Chemical Society
- Year
- 2001
- Tongue
- English
- Weight
- 70 KB
- Volume
- 66
- Category
- Article
- ISSN
- 0022-3263
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๐ SIMILAR VOLUMES
Introduction. ~ Stereoselective C-C bond forming reactions catalyzed by chiral transition-metal complexes are a topic of fundamental importance [l]. In 1986, Hayashi and Zto reported an elegant asymmetric synthesis of dihydrooxazoles by an efficient gold(1)-catalyzed coupling of aldehydes with 2-iso
Highly diastereoselective nucleophilic addition reactions of organometallic reagents to formyl[2.2]paracyclophane derivatives which were ortho-substituted by hydroxy-, alkoxy-and trimethylsilyloxy-groups are reported. The absolute configuration of the newly formed secondary alcohols is assigned on t