"Reduced" analogs of puromycin. Synthesis of 3'-O-(L-2-amino-3-phenylpropyl)-N6,N6-dimethyladenosine and the corresponding 2' isomer
- 1 September 1980
- journal article
- research article
- Published by American Chemical Society (ACS) in The Journal of Organic Chemistry
- Vol. 45 (20) , 4006-4010
- https://doi.org/10.1021/jo01308a012
Abstract
No abstract availableThis publication has 2 references indexed in Scilit:
- Simple models of nucleic acid interactions. 3. Aminoacyl derivatives of "bridged" nucleosides: chemical synthesis and substrate activity of 2'(3')-O-(N-acetyl)-L-leucyl-2''(3'')-O-L-phenylalanyl-(1,2-diadenosin-N6-yl)ethane, a spacer probe for ribosomal peptidyltransferaseBiochemistry, 1978
- Methylation of adenosine in strongly alkaline medium: preparation and properties of O'-methyl derivatives of adenosine and N6-methyladenosineBiochemistry, 1976