Abstract
The synthesis and NMR analysis of a 2′-O-alanyl, 3′-O-[1- 13C]valyl-pdCpA derivative has permitted the definitive assignment of the positions of acylation of tandemly activated pdCpAs, and the bisaminoacylated transfer RNAs derived therefrom.
| Original language | English (US) |
|---|---|
| Pages (from-to) | 3135-3138 |
| Number of pages | 4 |
| Journal | Organic and Biomolecular Chemistry |
| Volume | 5 |
| Issue number | 19 |
| DOIs | |
| State | Published - 2007 |
| Externally published | Yes |
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ASJC Scopus subject areas
- Biochemistry, Genetics and Molecular Biology(all)
- Chemistry(all)
Cite this
Positional assignment of differentially substituted bisaminoacylated pdCpAs. / Maloney, David J.; Ghanem, Noha; Zhou, Jia; Hecht, Sidney M.
In: Organic and Biomolecular Chemistry, Vol. 5, No. 19, 2007, p. 3135-3138.Research output: Contribution to journal › Article
}
TY - JOUR
T1 - Positional assignment of differentially substituted bisaminoacylated pdCpAs
AU - Maloney, David J.
AU - Ghanem, Noha
AU - Zhou, Jia
AU - Hecht, Sidney M.
PY - 2007
Y1 - 2007
N2 - The synthesis and NMR analysis of a 2′-O-alanyl, 3′-O-[1- 13C]valyl-pdCpA derivative has permitted the definitive assignment of the positions of acylation of tandemly activated pdCpAs, and the bisaminoacylated transfer RNAs derived therefrom.
AB - The synthesis and NMR analysis of a 2′-O-alanyl, 3′-O-[1- 13C]valyl-pdCpA derivative has permitted the definitive assignment of the positions of acylation of tandemly activated pdCpAs, and the bisaminoacylated transfer RNAs derived therefrom.
UR - http://www.scopus.com/inward/record.url?scp=34548761899&partnerID=8YFLogxK
UR - http://www.scopus.com/inward/citedby.url?scp=34548761899&partnerID=8YFLogxK
U2 - 10.1039/b708786a
DO - 10.1039/b708786a
M3 - Article
C2 - 17878972
AN - SCOPUS:34548761899
VL - 5
SP - 3135
EP - 3138
JO - Organic and Biomolecular Chemistry
JF - Organic and Biomolecular Chemistry
SN - 1477-0520
IS - 19
ER -