Stereoselective synthesis of the synthons having three consective chiral centers
β Scribed by Tadashi Nakata; Mineo Fukui; Hisatoshi Ohtsuka; Takeshi Oishi
- Publisher
- Elsevier Science
- Year
- 1983
- Tongue
- French
- Weight
- 250 KB
- Volume
- 24
- Category
- Article
- ISSN
- 0040-4039
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π SIMILAR VOLUMES
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Asymmetric Synthesis of Ξ²-Hydroxy Esters Having Three Consecutive Chiral Centers with a Reductase from Bakers' Yeast. -The title reaction is investigated with Ξ²-keto esters (I) having a secondary alkyl group at the Ξ±-position. The corresponding Ξ²-hydroxy esters can be isolated in excellent enantios
In order to synthesize erythromycin A from D-glucose as a chiral starting material, the left-hand segment of 9-dihydroerythronolide A having six consecutive chiral centers was synthesized by means of some stereoselective reactions in acyclic systems and MPM protection. In recent years, much attenti
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