@article { ISI:000231183000055,
	title = {Trans-5-Aminopipecolyl-aegPNA chimera: design, synthesis, and study of binding preferences with DNA/RNA in duplex/triplex mode},
	journal = {Journal of Organic Chemistry},
	volume = {70},
	number = {17},
	year = {2005},
	month = {AUG},
	pages = {6956-6959},
	publisher = {AMER CHEMICAL SOC},
	type = {Article},
	address = {1155 16TH ST, NW, WASHINGTON, DC 20036 USA},
	abstract = {<p>[GRAPHICS] The design and synthesis of novel chiral PNA monomer based on traps-5-aminopipecolic acid is reported. The trans diequatorial disposition of the 1,4 ring substituents in six-membered 5-aminopipecolic acid derivative could be favorable over trans 1,3 axial-equatorial disposition in 4-amino-pipecolic acid of PNA. Studies on the synthesis of traps-4/ 5-aminopipecolyl PNA-eagPNA chimeras and their binding preferences to DNA/RNA in duplex/triplex modes are described.</p>},
	issn = {0022-3263},
	doi = {10.1021/jo0506884},
	author = {Lonkar, P. S. and Kumar, V. A.}
}
