Synthesis of 3′-(L-2-amino-3-phenylpropyl)amino-3′-deoxy-N6,N6-dimethyladenosine - a new analog of puromycin
✍ Scribed by Tetsuo Kato; Jiří Žemlička
- Publisher
- Elsevier Science
- Year
- 1978
- Tongue
- French
- Weight
- 212 KB
- Volume
- 19
- Category
- Article
- ISSN
- 0040-4039
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Single-crystal X-ray study T = 190 K Mean '(C±C) = 0.005 A Ê R factor = 0.054 wR factor = 0.106 Data-to-parameter ratio = 9.0 For details of how these key indicators were automatically derived from the article, see http://journals.iucr.org/e.
6-Azido-3-oxa-2,3,4,6-tetradeoxy-D- and -L-glycero-hexopyranoses were synthesized in five steps from (2S)-and (2R)-1,2-O-isopropylideneglycerols, respectively. After conversion into the corresponding ethyl 1-thioglycosides, each was condensed with a protected derivative of 6-O-(3-amino-3-deoxy-alpha
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Dedicated to Professor Hitosi Nozaki on the occasion of his 60th birthday. Magnesium enolates of t-butyl (or ethyl) acetate and t-butyl propionate are found to react with nitriles to give 3-amino-2-alkenoates having Z configuration. The title compounds are versatile intermediates for the synthesis