Novel Enantioselective Synthesis of trans-α-(2-Carboxycycloprop-1yl)glycines: Conformationally Constrained L-Glutamate Analogues. -Key step of the described sequence is the oxazaborolidine-catalyzed enantioselective conversion of oxime ethers (V) and (VI) to the corresponding amines. Interestingly,
✦ LIBER ✦
ChemInform Abstract: Novel Open-Chain and Cyclic Conformationally Constrained (R)- and (S)-. alpha.,α-Disubstituted Tyrosine Analogues.
✍ Scribed by D. OBRECHT; C. LEHMANN; R. RUFFIEUX; P. SCHOENHOLZER; K. MUELLER
- Book ID
- 112024222
- Publisher
- John Wiley and Sons
- Year
- 2010
- Weight
- 41 KB
- Volume
- 26
- Category
- Article
- ISSN
- 0931-7597
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