Results
1 -
10 of
12
(Click
here to explore results)
- Modified internucleoside linkages for nuclease-resistant oligonucleotides. Guillaume Clavé, Maeva Reverte, Jean-Jacques Vasseur, Michael Smietana
, RSC Chem. Biol.
, 2021
, 2
, 94
- The synthesis of phosphorylated 3′-amino-3′-deoxythymidine and 5′-amino-5′-deoxythymidine. Ronald P. Glinski, M. Sami Khan, Richard L. Kalamas, Calvin L. Stevens, Michael B. Sporn
, J. Chem. Soc. D
, 1970
, 915
- The muraminomicin biosynthetic gene cluster and enzymatic formation of the 2-deoxyaminoribosyl appendage. Xiuling Chi, Satoshi Baba, Nidhi Tibrewal, Masanori Funabashi, Koichi Nonaka, Steven G. Van Lanen
, Med. Chem. Commun.
, 2013
, 4
, 239
- Supramolecular assemblies of novel aminonucleoside phospholipids and their bonding to nucleic acids. Delin Pan, Jing Sun, Hongwei Jin, Yating Li, Liyu Li, Yun Wu, Lihe Zhang, Zhenjun Yang
, Chem. Commun.
, 2015
, 51
, 469
- Synthesis, enzymatic stability and base-pairing properties of oligothymidylates containing thymidine dimers with different N-substituted guanidine linkages. Frank Vandendriessche, Arthur Van Aerschot, Martine Voortmans, Gerard Janssen, Roger Busson, An Van Overbeke, Walter Van den Bossche, Jos Hoogmartens, Piet Herdewijn
, J. Chem. Soc., Perkin Trans. 1
, 1993
, 1567
- Synthesis and duplex stability of oligodeoxyribonucleotides containing a 2′→5′-amide linkage. Mai-Yee Chan, Robin A. Fairhurst, Stephen P. Collingwood, Julie Fisher, John R. P. Arnold, Richard Cosstick, Ian A. O’Neil
, J. Chem. Soc., Perkin Trans. 1
, 1999
, 315
- A three-component reagent system for rapid and mild removal of O-, N- and S-trityl protecting groups. Máté Kicsák, Miklós Bege, Ilona Bereczki, Magdolna Csávás, Mihály Herczeg, Zoltán Kupihár, Lajos Kovács, Anikó Borbás, Pál Herczegh
, Org. Biomol. Chem.
, 2016
, 14
, 3190
- Structural modifications of the neomycin class of aminoglycosides. Smritilekha Bera, Dhananjoy Mondal, Subhadeep Palit, Frank Schweizer
, Med. Chem. Commun.
, 2016
, 7
, 1499
-
Synthesis, structure and reactions of uridine
2′-C,3′-O-γ-butyrolactone:
versatile intermediate for the synthesis of 2′-C-branched
nucleosides
. Anthony J. Lawrence, John B. J. Pavey, Mai-Yee Chan, Robin A. Fairhurst, Stephen P. Collingwood, Julie Fisher, Richard Cosstick, Ian A. O’Neil
, J. Chem. Soc., Perkin Trans. 1
, 1997
, 2761
- 5 Natural polymers—chemistry. Harri Lönnberg
, Annu. Rep. Prog. Chem., Sect. B: Org. Chem.
, 2001
, 97
, 177