Keyword search (4,163 papers available)

"Liu JT" Authored Publications:

Title Authors PubMed ID
1 Sterically-Hindered Molecular p-Dopants Promote Integer Charge Transfer in Organic Semiconductors Charoughchi S; Liu JT; Berteau-Rainville M; Hase H; Askari MS; Bhagat S; Forgione P; Salzmann I; 37220083
CHEMBIOCHEM
2 Preparation of a Convertible Spacer Containing a Disulfide Group for Versatile Functionalization of Oligonucleotides Pontarelli A; Liu JT; Oh JK; Wilds CJ; 36840706
CHEMBIOCHEM
3 Synthesis of a Convertible Linker Containing a Disulfide Group for Oligonucleotide Functionalization Pontarelli A; Liu JT; Movasat H; Ménard S; Oh JK; Wilds CJ; 35863757
CHEMBIOCHEM
4 Characterization of a recently synthesized microtubule-targeting compound that disrupts mitotic spindle poles in human cells Jaunky DB; Larocque K; Husser MC; Liu JT; Forgione P; Piekny A; 34880347
BIOLOGY
5 Design, structure-activity relationship study and biological evaluation of the thieno[3,2-c]isoquinoline scaffold as a potential anti-cancer agent Liu JT; Jaunky DB; Larocque K; Chen F; Mckibbon K; Sirouspour M; Taylor S; Shafeii A; Campbell D; Braga H; Piekny A; Forgione P; 34416378
BIOLOGY
6 Approaching the Integer-Charge Transfer Regime in Molecularly Doped Oligothiophenes by Efficient Decarboxylative Cross-Coupling Liu JT; Hase H; Taylor S; Salzmann I; Forgione P; 31961982
CHEMBIOCHEM

 

Title:Synthesis of a Convertible Linker Containing a Disulfide Group for Oligonucleotide Functionalization
Authors:Pontarelli ALiu JTMovasat HMénard SOh JKWilds CJ
Link:https://pubmed.ncbi.nlm.nih.gov/35863757/
DOI:10.1021/acs.orglett.2c02149
Publication:Organic letters
Keywords:
PMID:35863757 Category: Date Added:2022-07-22
Dept Affiliation: CHEMBIOCHEM
1 Department of Chemistry and Biochemistry, Faculty of Arts and Science, Concordia University, 7141 Rue Sherbrooke Ouest, Montréal, Québec H4B 1R6, Canada.

Description:

The synthesis and incorporation of a tosylated phosphoramidite linker containing a disulfide bond is described. Incorporation of the linker into short DNA and RNA oligomers proceeded efficiently using automated solid phase synthesis. Treatment of the support bound oligonucleotide followed by cleavage from the solid support provided a variety of common functional handles, expanding the strategies of bifunctional modification of synthetic oligonucleotides for conjugation applications.





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