Publication Type:

Conference Paper

Source:

Materials Today: Proceedings, Elsevier Ltd, Volume 5, Number 8, p.16580-16584 (2018)

URL:

https://www.scopus.com/inward/record.uri?eid=2-s2.0-85052922496&doi=10.1016%2fj.matpr.2018.06.014&partnerID=40&md5=87a4f9e56d9090ad5d3b74ddab3bd800

Abstract:

<p>Glycine based peptide nucleic acid (PNA) monomers are useful in the construction of PNA oligomers which are, in general, hydrophobic in nature. To overcome this huddle, serine based peptide nucleic acid (PNA) monomer was synthesized which will a good candidate in terms of increasing hydrophilicity. The synthesis involves in the alkylation of N-bromoethyl phthalimide on nosyl protected serine methyl ester followed by deprotection and condensation with nucleobase yields PNA monomer. The phthalimide group on nitrogen serves as protecting group as well as marker. © 2017 Elsevier Ltd.</p>

Notes:

cited By 0; Conference of 2016 International Conference on Advanced Materials, SCICON 2016 ; Conference Date: 19 December 2016 Through 21 December 2016; Conference Code:138807

Cite this Research Publication

S. Sivakumar, Ramani, P., and Shilpa, G. S., “Phthalimido protected peptide nucleic acid monomer - Synthesis and Characterization”, in Materials Today: Proceedings, 2018, vol. 5, pp. 16580-16584.