Photolabile group for 5′-OH protection of nucleosides: synthesis and photodeprotection rate
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[1] Xiangqin Cui,et al. Sensors and Actuators B , 2003 .
[2] S. Braslavsky,et al. Chemical actinometry , 1989, Chemistry International.
[3] Nam Quoc Ngo,et al. The Efficiency of Light-Directed Synthesis of DNA Arrays on Glass Substrates , 1997 .
[4] C. Holmes. Model Studies for New o-Nitrobenzyl Photolabile Linkers: Substituent Effects on the Rates of Photochemical Cleavage. , 1997, The Journal of organic chemistry.
[5] R. S. Foote,et al. Photolabile protecting groups for nucleosides: Synthesis and photodeprotection rates , 1997 .
[6] Michael C. Pirrung,et al. Comparison of Methods for Photochemical Phosphoramidite-Based DNA Synthesis , 1995 .
[7] B. Gaffney,et al. TRANSIENT PROTECTION: EFFICIENT ONE‐FLASK SYNTHESES OF PROTECTED DEOXYNUCLEOSIDES , 2002 .
[8] B. Gaffney,et al. Transient protection: efficient one-flask syntheses of protected deoxynucleosides , 1982 .
[9] R. Zepp. Quantum yields for reaction of pollutants in dilute aqueous solution , 1978 .
[10] C. A. Parker,et al. A new sensitive chemical actinometer - II. Potassium ferrioxalate as a standard chemical actinometer , 1956, Proceedings of the Royal Society of London. Series A. Mathematical and Physical Sciences.