Stereoselective formation of a 2′(3′)-aminoacyl ester of a nucleotide
✍ Scribed by Arthur L. Weber
- Publisher
- Springer
- Year
- 1987
- Tongue
- English
- Weight
- 445 KB
- Volume
- 25
- Category
- Article
- ISSN
- 0022-2844
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📜 SIMILAR VOLUMES
## Abnticx : A MW 6ynthend 04 ~2-buttnotidti ih de.bcLbcd which .&o&m h.kt&Oh&Lc-Live condenntion 06 an cx-htiyt uteh anion ukth an cu-hetoacefal. Unsaturated five membered ring lactones, butenolides, occur widely in nature and display a wide range of interesting properties (1). Despite the great
## Abstract We report the synthesis of a modified 8mer RNA sequence, (C‐C‐C‐C‐A‐C‐C‐(2′‐thio)A)‐RNA 5′‐(dihydrogen phosphate) (**9**) containing a 3′‐terminal 2′‐thioadenosine (__Schemes 2__ and __3__), and its spontaneous and site‐specific aminoacylation with the weakly activated amino acid thioes