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
✦ LIBER ✦
Stereoselective synthesis of (2R,3S,4S,5R)-trans-3,4-dihydroxy-5-(4-fluorophenoxymethyl)-2-(1-N-hydroxyureidyl-3-butyn-4-yl)tetrahydrofuran and (2R,3S,4S,5R)-trans-5-ethynyl-2-(4-fluorophenoxymethyl)-3,4-O-isopropylidene tetrahydrofuran from mannose diacetonide
✍ Scribed by G.V.M. Sharma; Sreenivas Punna; Lanka Hymavathi; N. Yella Reddy; Palakodety Radha Krishna; Mukund S. Chorghade; Steven V. Ley
- Book ID
- 108283915
- Publisher
- Elsevier Science
- Year
- 2005
- Tongue
- English
- Weight
- 158 KB
- Volume
- 16
- Category
- Article
- ISSN
- 0957-4166
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