The Journal of Organic Chemistry

A Convenient Method for the Synthesis of N-Free 5'-O-(p, p'-Dimethoxytrityl)-2'-deoxyribonucleosides via the 5'-O-Selective Tritylation of the Parent Substances

M Kataoka, Y Hayakawa

Index: Kataoka, Masanori; Hayakawa, Yoshihiro Journal of Organic Chemistry, 1999 , vol. 64, # 16 p. 6087 - 6089

Full Text: HTML

Citation Number: 14

Abstract

5′-O-(p, p′-Dimethoxytrityl)-2′-deoxyribonucleosides without protection of the amino functions, 5-8, are important substances for the synthesis of various kinds of nucleic acid- related derivatives. For example, these compounds are useful as building blocks for oligonucleotide synthesis via the hydroxyl-activation method. 1 They have also served as key intermediates of N-free nucleoside-3′-phosphoramidites2, 3 and-H-phosphonates, 4 ...

Related Articles:

Facile synthesis of oligodeoxyribonucleotides via the phosphoramidite method without nucleoside base protection

[Hayakawa, Yoshihiro; Kataoka, Masanori Journal of the American Chemical Society, 1998 , vol. 120, # 48 p. 12395 - 12401]

2-(Azidomethyl) benzoyl as a new protecting group in nucleosides

[Wada, Takeshi; Ohkubo, Akihiro; Mochizuki, Akira; Sekine, Mitsuo Tetrahedron Letters, 2001 , vol. 42, # 6 p. 1069 - 1072]

Nucleotide chemistry. 16. Amidine protecting groups for oligonucleotide synthesis

[McBride, Lincoln J.; Kierzek, Ryszard; Beaucage, Serge L.; Caruthers, Marvin H. Journal of the American Chemical Society, 1986 , vol. 108, # 8 p. 2040 - 2048]

2-(Azidomethyl) benzoyl as a new protecting group in nucleosides

[Wada, Takeshi; Ohkubo, Akihiro; Mochizuki, Akira; Sekine, Mitsuo Tetrahedron Letters, 2001 , vol. 42, # 6 p. 1069 - 1072]

Nucleotide chemistry. 16. Amidine protecting groups for oligonucleotide synthesis

[McBride, Lincoln J.; Kierzek, Ryszard; Beaucage, Serge L.; Caruthers, Marvin H. Journal of the American Chemical Society, 1986 , vol. 108, # 8 p. 2040 - 2048]

More Articles...