Organic Letters · 2007 · 11 citations · 30 references
PharmacyChemistryNucleic Acid BiochemistryNucleic Acid ChemistryOrganic ChemistryCross-coupling ReactionsNucleic Acid SynthesisNucleobase ChemistryOligonucleotide ChemistryOrganic SynthesisModified NucleobasesNucleobase AnaloguesNucleobase StructureNucleobase SynthesisPurine ChemistryPyrimidine ChemistrySonogashira CouplingSynthetic Nucleobases
A series of homo- and heteroditopic thymine- and/or adenine-terminated molecules incorporating rigid aryl or oligo(phenylene ethynylene) linkers has been efficiently synthesized. The key steps involved in the synthesis are the construction of the N-arylated nucleobases using the Chan-Lam-Evans-modified Ullman coupling and their further elaboration using the Sonogashira coupling. Furthermore, the synthesis of a rigid tripodal thymine derivative is reported.
30
Folding DNA to create nanoscale shapes and patterns
Paul W. K. Rothemund · Nature · 2006 · 7.4K citations
Design and self-assembly of two-dimensional DNA crystals
Erik Winfree, Furong Liu, Lisa A. Wenzler et al. · Nature · 1998 · 2.9K citations
DNA-Templated Self-Assembly of Protein Arrays and Highly Conductive Nanowires
Hao Yan, Sung Ha Park, Gleb Finkelstein et al. · Science · 2003 · 1.8K citations