Photoacid generators for the synthesis of oligo-DNA in a...

Synthetic resins or natural rubbers -- part of the class 520 ser – Synthetic resins – Compositions to be polymerized by wave energy wherein said...

Reexamination Certificate

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C522S031000, C522S057000, C522S059000, C568S926000, C568S927000, C568S936000, C568S937000, C568S938000, C430S005000, C430S270100, C430S313000, C430S326000, C430S905000, C430S913000, C430S919000, C430S926000, C514S741000, C514S740000, C523S300000

Reexamination Certificate

active

07964654

ABSTRACT:
Compounds represented by the following structural formulas can be used as photoacid generators:Such compounds are useful, for example, in fabricating arrays of polymers.

REFERENCES:
patent: 4996136 (1991-02-01), Houlihan et al.
patent: 5135838 (1992-08-01), Houlihan et al.
patent: 5200544 (1993-04-01), Houlihan et al.
patent: 6083697 (2000-07-01), Beecher et al.
patent: 6159665 (2000-12-01), Chin et al.
patent: 6310083 (2001-10-01), Kao et al.
patent: 7332477 (2008-02-01), Cammack et al.
patent: 7544721 (2009-06-01), Gaud et al.
patent: 2004/0110133 (2004-06-01), Xu et al.
patent: 2005/0037401 (2005-02-01), Cammack et al.
patent: 2009/0270279 (2009-10-01), Serafinowski et al.
patent: WO 2006117556 (2006-11-01), None
Amit et al., “Photosensitive Protecting Groups—A Review,” Israel Journal of Chemistry, 1974, 12 (1-2): 103-113.
Barzynski et al., “Zur Photolyse von Makromolekularen o-Nitrobenzyl Derivaren,” Die Angewandte Makromolekularchemie. vol. 93 (1981), pp. 131-141.
Dussy et al. “New Light-Sensitive Nucleosides for Caged DNA Strand Breaks,” ChemBioChem, (2002), 3(1): 54-60.
Gao et al., “Oligonucleotide Synthesis Using Solution Photogenerated Acids,” (1998) Journal of the American Chemical Society 120(48): 12698-12699.
Houlihan et al., Design, Synthesis, Characterization, and Use of All-Organic Nonionic Photogenerators of Acid, (1991), 3(3): 462-471.
Reichmanis et al.,“O-nitrobenzyl photochemistry: Solution vs. solid-state behavior,” Journal of Polymer Science: Polymer Chemistry Edition, (1985), 23(1): 1-8.
Reichmanis et al., “A Study of the Photochmical Response of o-Nitrobenzyl Cholate Derivatives in P (MMA-MAA) Matrices,” Journal of Polymer Science: Polymer Chemistry Ed. (1983), vol. 21, pp. 1075-1083.
Robles et al., “Photochemical Release of Aldehydes from α-Acetoxy Nitroveratryl Ethers,” Organic Letters, (2005), 7(16): 3545-3547.
Tsao et al., “Matrix and Time-Resolved Infrared Spectroscopy of Chloro-p-Nitrophenylcarbene and Related Species,” Journal of Physical Chemistry: Part A. (2001), vol. 105, pp. 8413-8416.
Walbert et al., “Photolabile Protecting Groups for Nucleosides: Mechanistic Studies of the 2-(2-Nitrobenzyl) ethyl Group,” Helevetica Chimica Aeta vol. 84, (2001), pp. 1601-1611.

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