Letters in Organic Chemistry

Author(s): Mitsuo Sekine, Masanori Tobe, Takashi Nagayama and Takeshi Wada

DOI: 10.2174/1570178043488419

Synthesis of N-(Trimethylsilylethoxycarbonyl)-deoxycytidine and Deoxyadenosine Derivatives as Key Intermediates for the DNA Synthesis using Fluoride Ion-Promoted Deprotection Strategy

Page: [179 - 182] Pages: 4

  • * (Excluding Mailing and Handling)

Abstract

An improved method for the synthesis of trimethylsilylethyl chloroformate (Teoc-Cl) was studied in great detail. N-Teoc-adenosine, N-Teoccytidine and their deoxyribonucleoside derivatives were synthesized as the key synthetic intermediates for the synthesis of base-sensitive oligonucleotide derivatives by use of N-methylimidazole. The stability and chemical properties of these Nprotected nucleoside derivatives were examined.

Keywords: teoc group, base-sensitive, n-protected nucleosides, dna/rna chemical synthesis