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SYNTHESIS OF (1 R ,3 S )-3-AMINO-1,2,2-TRIMETHYLCYCLOPENTYLMETHANOL
✍ Scribed by Blanco, José M.; Caamaño, Olga; Fernández, Franco; García-Mera, Xerardo; Rodríguez, José E.
- Book ID
- 127324863
- Publisher
- Taylor and Francis Group
- Year
- 1998
- Tongue
- English
- Weight
- 478 KB
- Volume
- 30
- Category
- Article
- ISSN
- 0030-4948
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📜 SIMILAR VOLUMES
The litle anlinomethyl (5) and amino (6) alcohols, which are of interest as intermediates in the synthesis of carbocyclic analogues of nucleosides, were prepared from (+)-camphoric acid via methyl (1S,3R)-3-carbamoyl-2.3.3-trimelhylcyclopel~tane earboxylale (8). Direct reduction of S gave 5 in 26% y
## 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