Simple stereoselective synthesis of (1E,3Z)-4-(substituted)amino 1,3-diethoxycarbonyl-1,3-butadienes
β Scribed by M. Akram Khan; Harry Adams
- Publisher
- Elsevier Science
- Year
- 1999
- Tongue
- French
- Weight
- 121 KB
- Volume
- 40
- Category
- Article
- ISSN
- 0040-4039
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β¦ Synopsis
Ethyl propynoate reacted with esters of amino acids in methanolic solutions containing sodium acetate to yield the title compounds la-d in 40-52% yields. Some aromatic amines similarly reacted with ethyl propynoate to yield the dienes 3a-h in relatively poor yields (17-45%).
π SIMILAR VOLUMES
A two step, totally stereoselective synthesis of (E,E)-lA-dialkoxy-l,3-butadienes from chiral secondary alcohols has been developed. The key step involves the regio-and stereoselective hydrozirconation of alkoxyethynes derived from chiral alcohols; the intermediate (E)-(2alkoxyvinyl)zircouium compou
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