Adenine, thymine and cytosine PNA monomers have been prepared using 3-amino-1,2-propanediol as a starting material. The benzoyl group was used to protect the exocyclic amines of the heterocyclic bases of A and C PNA monomers and the backbone primary amine was protected with the monomethoxytrityl group. The thymine and cytosine PNA monomers were used in conjunction with standard DNA synthesis monomers to produce chimeric PNA DNA (PDC) oligomers. Ultraviolet melting studies confirmed that these oligomers form stable hybrids with complementary DNA strands and that mismatches in the DNA but more so in the PNA sections lead to duplex destabilisation
Synthetic methods were developed for the preparation of several structurally diverse aromatic pepti...
In recent times, PNA (I), a structural mimic of DNA in which the sugar-phosphate backbone is replace...
A systematic study to evaluate the ability of 5'-DNA-3'-p-(N)-PNA-(C) chimeras to form triple helix ...
Adenine, thymine and cytosine PNA monomers have been prepared using 3-amino-1,2-propanediol as a sta...
The chemical synthesis of thymine, cytosine and adenine Peptide Nucleic Acid (PNA) monomers, incorpo...
A new synthetic strategy to get the PNA–3′DNA linker with the monomethoxytrityl (Mmt) group as tempo...
Oligonucleotides carrying a peptide nucleic acid (PNA) tail at the 3′-end have been efficiently prep...
Oligonucleotides carrying a peptide nucleic acid (PNA) tail at the 3'-end have been efficiently prep...
The synthesis and structural characterization of four PNA-DNA chimeras - (5')TGGG(3')-t (C1), (5')TG...
Peptide nucleic acids (PNAs) are oligonucleotide mimics in which the sugar-phosphate backbone has be...
Peptide nucleic acids (PNAs) are oligonucleotide mimics in which the sugar-phosphate backbone has be...
In order to investigate the role played by the aromatic moiety of Aromatic Peptide Nucleic Acids (A...
Peptide nucleic acids (PNAs) are oligonucleotide mimics in which the sugar-phosphate backbone has b...
This paper describes chemical synthesis of prolyl PNAs which are a class of conformationally constra...
A pentadecanucleotide was prepared from 1-a-arabinofuranosylthymine. This novel oligonucleotlde was ...
Synthetic methods were developed for the preparation of several structurally diverse aromatic pepti...
In recent times, PNA (I), a structural mimic of DNA in which the sugar-phosphate backbone is replace...
A systematic study to evaluate the ability of 5'-DNA-3'-p-(N)-PNA-(C) chimeras to form triple helix ...
Adenine, thymine and cytosine PNA monomers have been prepared using 3-amino-1,2-propanediol as a sta...
The chemical synthesis of thymine, cytosine and adenine Peptide Nucleic Acid (PNA) monomers, incorpo...
A new synthetic strategy to get the PNA–3′DNA linker with the monomethoxytrityl (Mmt) group as tempo...
Oligonucleotides carrying a peptide nucleic acid (PNA) tail at the 3′-end have been efficiently prep...
Oligonucleotides carrying a peptide nucleic acid (PNA) tail at the 3'-end have been efficiently prep...
The synthesis and structural characterization of four PNA-DNA chimeras - (5')TGGG(3')-t (C1), (5')TG...
Peptide nucleic acids (PNAs) are oligonucleotide mimics in which the sugar-phosphate backbone has be...
Peptide nucleic acids (PNAs) are oligonucleotide mimics in which the sugar-phosphate backbone has be...
In order to investigate the role played by the aromatic moiety of Aromatic Peptide Nucleic Acids (A...
Peptide nucleic acids (PNAs) are oligonucleotide mimics in which the sugar-phosphate backbone has b...
This paper describes chemical synthesis of prolyl PNAs which are a class of conformationally constra...
A pentadecanucleotide was prepared from 1-a-arabinofuranosylthymine. This novel oligonucleotlde was ...
Synthetic methods were developed for the preparation of several structurally diverse aromatic pepti...
In recent times, PNA (I), a structural mimic of DNA in which the sugar-phosphate backbone is replace...
A systematic study to evaluate the ability of 5'-DNA-3'-p-(N)-PNA-(C) chimeras to form triple helix ...