Kashida, Hiromu; Nishikawa, Keiji; Ito, Yuka; Murayama, Keiji; Hayashi, Ichiyo; Kakuta, Takahiro; Ogoshi, Tomoki; Asanuma, Hiroyuki published their research in Chemistry – A European Journal in 2021. The article was titled 《A Pyrene-Modified Serinol Nucleic Acid Nanostructure Converts the Chirality of Threoninol Nucleic Acids into Circularly Polarized Luminescence Signals》.Recommanded Product: 534-03-2 The article contains the following contents:
Herein is reported a circularly polarized luminescent (CPL) probe that can respond to the chirality of nucleic acids. An achiral nanostructure was prepared by the hybridization of sym. serinol nucleic acid (SNA) containing pyrene-modified residues. When chiral oligomers that were complementary to the SNA were added, they induced helicity into the SNA nanowire. Efficient CD (CD) signal amplification was observed when pyrene was attached to uracil bases through a rigid alkynyl linker. Both CPL and CD signals were observed; they depended on the chirality of the added acyclic threoninol nucleic acid (aTNA) oligomer. This system can be used to convert the chirality of chiral biomols. into chiroptical signals. In the experimental materials used by the author, we found 2-Aminopropane-1,3-diol(cas: 534-03-2Recommanded Product: 534-03-2)
2-Aminopropane-1,3-diol(cas: 534-03-2) belongs to anime. The reaction of alkyl halides, R―X, where X is a halogen, or analogous reagents with ammonia (or amines) is useful with certain compounds. Not all alkyl halides are effective reagents; the reaction is sluggish with secondary alkyl groups and fails with tertiary ones. Its usefulness is largely confined to primary alkyl halides (those having two hydrogen atoms on the reacting site).Recommanded Product: 534-03-2
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