| Literature DB >> 7079181 |
E Ohtsuka, Y Taniyama, R Marumoto, H Sato, H Hirosaki, M Ikehara.
Abstract
A phosphorylating reagent o-chlorophenyl phosphoro-p-anisi-dochloridate was synthesized to phosphorylate the 3'-hydroxyl group of N, 5'-protected deoxynucleosides. These nucleotides served as 3'-terminal units for the synthesis of oligonucleotide blocks. By condensation of these oligonucleotide blocks the partially complementary deoxypentadecanucleotides dAGCTTATAATGC-TCG and dAGCTCGAGCATTATA, which contained the ideal Pribnow sequence TATAATG, were synthesized.Entities:
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Year: 1982 PMID: 7079181 PMCID: PMC320636 DOI: 10.1093/nar/10.8.2597
Source DB: PubMed Journal: Nucleic Acids Res ISSN: 0305-1048 Impact factor: 16.971