Synthesis of (2S, 3R, 4S), (2S, 3S, 4R)-epoxyprolines and aminohydroxyprolines
β Scribed by J. Kenneth Robinson; Victor Lee; Timothy D.W. Claridge; Jack E. Baldwin; Christopher J. Schofield
- Book ID
- 108378862
- Publisher
- Elsevier Science
- Year
- 1998
- Tongue
- French
- Weight
- 888 KB
- Volume
- 54
- Category
- Article
- ISSN
- 0040-4020
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π 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
## Synthesis and transformations of (1R,2R,3S,4R)-4-O- benzylhydroxylamino-2,3-O-isopropylidene-1,2,3-cyclopentanetrioh synthesis of (1S,2R,3S,4R)-4-amino-2,3-O-isopropylidene-l,2,3cyclopentanetriol
A catalytic deuteration of protected 3,4-dehydro-L-proline using RuCI2(PPh3) 3 followed by RuO~-oxidation gave a 3,4-dideuterated L-pyroglutamic acid derivative which is considered to be a promising precursor for various deuterated amino acids. The present study demonstrates a stereoselective reduct