Keyword search (4,163 papers available)

"Kumar R" Authored Publications:

Title Authors PubMed ID
1 Developing and Sustaining Dementia Capable Communities: An Analysis of the Current Evidence Biglieri S; Ahmed N; Main S; Tupling OL; Vijayakumar R; Boger J; Daum C; Dupuis S; Koch M; Liu L; Lopez K; Mann J; Martin M; McAiney C; Nasir HJ; Nasir N; Pearce B; Weldrick R; Vanderlinden K; Middleton L; 41432943
ENCS
2 Interrogation of Bacillus anthracis SrtA active site loop forming open/close lid conformations through extensive MD simulations for understanding binding selectivity of SrtA inhibitors Selvaraj C; Selvaraj G; Mohamed Ismail R; Vijayakumar R; Baazeem A; Wei DQ; Singh SK; 34220215
BIOLOGY
3 Characterization of Phase I and Glucuronide Phase II Metabolites of 17 Mycotoxins Using Liquid Chromatography-High-Resolution Mass Spectrometry Slobodchikova I; Sivakumar R; Rahman MS; Vuckovic D; 31344861
CBAMS
4 Tuning of Morphology and Stability of Gold Nanostars Through pH Adjustment. Kumar R, Badilescu S, Packirisamy M 30913757
ENCS
5 Directing the Viedma ripening of ethylenediammonium sulfate using "Tailor-made" chiral additives. Nguyen TP, Cheung PS, Werber L, Gagnon J, Sivakumar R, Lennox C, Sossin A, Mastai Y, Cuccia LA 27722259
CHEMBIOCHEM

 

Title:Directing the Viedma ripening of ethylenediammonium sulfate using "Tailor-made" chiral additives.
Authors:Nguyen TPCheung PSWerber LGagnon JSivakumar RLennox CSossin AMastai YCuccia LA
Link:https://www.ncbi.nlm.nih.gov/pubmed/27722259?dopt=Abstract
Publication:
Keywords:
PMID:27722259 Category:Chem Commun (Camb) Date Added:2019-05-31
Dept Affiliation: CHEMBIOCHEM
1 Department of Chemistry & Biochemistry, Concordia University, 7141 Sherbrooke Street West, Montréal, Québec H4B 1R6, Canada. Louis.Cuccia@concordia.ca.
2 Bar-Ilan University, Department of Chemistry, Ramat Gan, Israel. Yitzhak.Mastai@biu.ac.il.

Description:

Directing the Viedma ripening of ethylenediammonium sulfate using "Tailor-made" chiral additives.

Chem Commun (Camb). 2016 Oct 18;52(85):12626-12629

Authors: Nguyen TP, Cheung PS, Werber L, Gagnon J, Sivakumar R, Lennox C, Sossin A, Mastai Y, Cuccia LA

Abstract

Both enantiomers of trans-cyclohexane-1,2-diammonium sulfate and trans-1,2-diphenylethylenediammonium sulfate were used as "tailor-made" additives to direct the mirror-symmetry breaking in the attrition-enhanced deracemization (i.e. Viedma ripening) of conglomerate crystals of ethylenediammonium sulfate (EDS). Isothermal titration calorimetry (ITC) shows chiral recognition of (1R,2R)- and (1S,2S)-1,2-diphenylethylenediamine to EDS crystals where the enthalpy of adsorption of the (1R,2R)-isomer on l-EDS crystals is higher in comparison to that on d-EDS crystals. These results are consistent with a "rule of reversal" mechanism driving the chiral outcome of the Viedma ripening of EDS.

PMID: 27722259 [PubMed]





BookR developed by Sriram Narayanan
for the Concordia University School of Health
Copyright © 2011-2026
Cookie settings
Concordia University