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- Reaction between 2′,3′,5′-tri-O-acetyladenosine and aryl chloroformates. 2′,3′,5′-Tri-O-acetyl-N(6)-phenoxycarbonyladenosine as an intermediate in the synthesis of 6-ureidopurine ribosides. P. Anne Lyon, Colin B. Reese
, J. Chem. Soc., Perkin Trans. 1
, 1978
, 131
- The structures of di-N-aroyl derivatives of adenosine and 2-amino-pyridine. P. Anne Lyon, Colin B. Reese
, J. Chem. Soc., Perkin Trans. 1
, 1974
, 2645
- Chemoenzymatic synthesis of cytokinins from nucleosides: ribose as a blocking group. Vladimir E. Oslovsky, Pavel N. Solyev, Konstantin M. Polyakov, Cyril S. Alexeev, Sergey N. Mikhailov
, Org. Biomol. Chem.
, 2018
, 16
, 2156
- Efficient access to 3′-O-phosphoramidite derivatives of tRNA related N
6-threonylcarbamoyladenosine (t6A) and 2-methylthio-N
6-threonylcarbamoyladenosine (ms2t6A). Katarzyna Debiec, Elzbieta Sochacka
, RSC Adv.
, 2021
, 11
, 1992
- Nucleotides. Part XXVII. The structures of adenylic acids a and b. D. M. Brown, G. D. Fasman, D. I. Magrath, A. R. Todd
, J. Chem. Soc.
, 1954
, 1448
- Labeling of organic biomolecules with ethynylferrocene. Evdoxia Coutouli-Argyropoulou, Maria Tsitabani, Georgios Petrantonakis, Aris Terzis, Catherine Raptopoulou
, Org. Biomol. Chem.
, 2003
, 1
, 1382
- Synthesis of the 3′-terminal half of yeast alanine transfer ribonucleic acid (tRNAAla) by the phosphotriester approach in solution. Part 1. Preparation of the nucleoside building blocks. Jonathan M. Brown, Chris Christodoulou, Simon S. Jones, Anil S. Modak, Colin B. Reese, Samson Sibanda, Aiko Ubasawa
, J. Chem. Soc., Perkin Trans. 1
, 1989
, 1735
- Some aspects of the chemistry of N(1)- and N(6)-dimethylallyl derivatives of adenosine and adenine. D. M. G. Martin, C. B. Reese
, J. Chem. Soc. C
, 1968
, 1731
- Efficient and green approach for the complete deprotection of O-acetylated biomolecules. Anthony Dunne, Jose M. Palomo
, RSC Adv.
, 2016
, 6
, 88974
- Aminolysis and alkaline hydrolysis of protected 1-hydroxybenzo-triazol-1-yl esters of adenosine 5′-phosphorothioate and -phosphorodithioate. Colin B. Reese, Louise H. K. Shek, Zhengyun Zhao
, J. Chem. Soc., Perkin Trans. 1
, 1995
, 3077