Synthesis of substituted chiral piperazinones as building blocks for peptidomimetics
โ Scribed by Kolter, Thomas ;Dahl, Christina ;Giannis, Athanassios
- Publisher
- John Wiley and Sons
- Year
- 1995
- Tongue
- English
- Weight
- 533 KB
- Volume
- 1995
- Category
- Article
- ISSN
- 0947-3440
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โฆ Synopsis
A new approach to 3,6-disubstituted chiral piperazinones 6a, b and ?a, b from D-glucosamine hydrochloride (1) or N-Z-Dglucosamine (8) and L-amino acid derivatives 2a, b or 9a, b is presented. Both final products and the intermediate pseudopeptides constitute valuable starting materials for the synthesis of peptidomimetics.
๐ SIMILAR VOLUMES
## Abstract For Abstract see ChemInform Abstract in Full Text.
The present paper describes the synthesis of 5-azido-6-ketones ( 14) and 6-hydroxy-5-ketone (20) from Hajos Wiechert ketone as chiral building blocks for cephalostatin analogues . The synthesis of symmetric cephalostatin analogue from 6-hydroxy-5-ketone has also been reported. The characterization o
For recent reviews and highlights on dendrimers, see [I]. ' ) The compound that would result from the reduction of 10 can, however, be prepared by a simpler procedure, see Scheme 2.