Stereocontrolled Synthesis of Methyl αR,2S,3R-3-(l-Acetoxyethyl)-1- (4-methoxyphenyl)-4-oxoazetidine-2-carboxylate
✍ Scribed by Zoltán Madarász; Ildikó Németh; Paul Toscano; John Welch; József Nyitrai
- Publisher
- Elsevier Science
- Year
- 1995
- Tongue
- French
- Weight
- 181 KB
- Volume
- 36
- Category
- Article
- ISSN
- 0040-4039
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📜 SIMILAR VOLUMES
The synthesis of 46 derivatives of (2R,3R,4S)-2-(aminomethyl)pyrrolidine-3,4-diol is reported (Scheme 1 and Fig. 3), and their inhibitory activities toward a-mannosidases from jack bean (B) and almonds (A) are evaluated (Table ). The most-potent inhibitors are (2R,3R,4S)-2-{[([1,1'-biphenyl]-4-ylmet
## Abstract The hydroperoxy endoperoxide **3**, obtained by photooxygenation of isotetralin (= 1,4,5,8‐tetrahydronaphthalene; **1**), was reduced with thiourea, and the resulting intermediate **4** was converted, after acetylation with acetyl chloride, to the interesting, double‐chlorinated acetate