Current Protocols in Nucleic Acid Chemistry by Martin Egli, Piet Herdewijn, Akira Matusda

By Martin Egli, Piet Herdewijn, Akira Matusda

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Science 238:336-341. J. J. 1981. Nucleic acid related compounds. 31. Smooth and efficient palladium-copper catalyzed coupling of terminal alkynes with 5-iodouracil nucleosides. Tetrahedron Lett. 22:421-424. J. J. 1983. Nucleic acid related compounds. 39. Efficient conversation of 5-iodo to 5-alkynyl and derived 5-substituted uracil bases and nucleosides. J. Org. Chem. 48:1854-1862. , and Otvos, L. 1993. Basemodified oligodeoxynucleotides. I. Effect of 5-alkyl, 5-(1-alkenyl) and 5-(1-alkynyl) substitution of the pyrimidines on duplex stability a n d h y d r o p h o b i c i t y.

1989. Synthesis and characterization of DNA oligomers and duplex containing covalently attached molecular labels: Comparison of biotin, fluorescin, and pyrene labels by thermodynamic and optical spectroscopic measurements. J. Am. Chem. Soc. 111:6966-6976. Contributed by Mohammad Ahmadian Cerus Corp. Concord, California Douglas A. Klewer Texas A&M University College Station, Texas Donald E. 2 M1G-deoxyribose (M1G-dR, 1,N2-pyrimido[1,2-α]purin-10(3H)-one, or pyrimidopurinone; see structure in Fig.

1989. Synthesis and characterization of DNA oligomers and duplex containing covalently attached molecular labels: Comparison of biotin, fluorescin, and pyrene labels by thermodynamic and optical spectroscopic measurements. J. Am. Chem. Soc. 111:6966-6976. Contributed by Mohammad Ahmadian Cerus Corp. Concord, California Douglas A. Klewer Texas A&M University College Station, Texas Donald E. 2 M1G-deoxyribose (M1G-dR, 1,N2-pyrimido[1,2-α]purin-10(3H)-one, or pyrimidopurinone; see structure in Fig.

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