Nasri Nesnas

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Name: Nesnas, Nasri
Organization: Florida Institute of Technology , USA
Department: Department of Chemistry
Title: Associate(PhD)

TOPICS

Co-reporter:Gloria Proni, Peter Cohen, Lesley-Ann Huggins, Nasri Nesnas
Forensic Science International 2017 Volume 280(Volume 280) pp:
Publication Date(Web):1 November 2017
DOI:10.1016/j.forsciint.2017.09.005
•Identification of a nonoxynol mixture in vaginal fluid and condoms’ residues.•Detection of a nonoxynol mixture in vaginal samples collected 8 h after intercourse was achieved.•Different sample preparation and instrument setting methods were explored.In this study we demonstrate the use of Direct Analysis in Real Time Mass Spectrometry (DART) as a powerful tool for detection of nonoxynol in vaginal fluid post contact with a condom, enabling rapid tracing and added evidences in sexual assault crimes. Vaginal fluid was sampled using cotton swabs and glass rods and measured directly with DART. Sample preparation using water, hexane, methanol, and dichloromethane extraction, was explored for comparison and optimization of signals. Nonoxynol was detected up to eight hours after sampling. Optimal sampling conditions and mass spectrometry parameters are reported and discussed.Download high-res image (135KB)Download full-size image
Co-reporter:Richard L. Comitz, Yannick P. Ouedraogo, Nasri Nesnas
Analytical Chemistry Research 2015 Volume 3() pp:20-25
Publication Date(Web):March 2015
DOI:10.1016/j.ancr.2014.11.001

Highlights

We present an unambiguous method to evaluate the efficiency of Photoprotective groups.

Traditional UV–vis methods are only truly effective with mononitrated indolinyl systems.

Using NMR integration of specific protons enabled a clear assessment of photolytic efficiency.

Introduction of a second nitro group in indolinyl system does improve efficiency of release by at least 5.8 folds.

Co-reporter:Yannick P. Ouedraogo;Longchuan Huang;Mariana P. Torrente;Gloria Proni;Ekaterina Chadwick;Rudolf J. Wehmschulte
Chirality 2013 Volume 25( Issue 9) pp:575-581
Publication Date(Web):
DOI:10.1002/chir.22186

ABSTRACT

A two-step stereoselective preparation of a goldfish pheromone, 17α,20β-dihydroxy-4-pregnen-3-one, is reported from the readily available cortexolone in 64% overall yield. The (20S)-epimer was also synthesized in three steps from cortexolone with an overall yield of 47%. A microscale chiroptical technique based on a host/guest complexation mechanism between the substrate and a dimeric metalloporphyrin host (tweezer) was used to confirm the stereochemical assignment, while Density Functional Theory (DFT) calculations were employed to explain the high stereoselectivity induced by the 17α-hydroxyl and C18-methyl groups. Chirality 00:000–000:, 2013. © 2013 Wiley Periodicals, Inc.

Co-reporter:Kafui Kpegba, Amegnona Agbonon, Ana G. Petrovic, Etchri Amouzou, Messanvi Gbeassor, Gloria Proni, and Nasri Nesnas
Journal of Natural Products 2011 Volume 74(Issue 3) pp:455-459
Publication Date(Web):November 11, 2010
DOI:10.1021/np100090e
The root bark of Cassia sieberiana was analyzed using direct analysis in real time mass spectrometry, and a main flavonoid component with an [M + H]+ mass of 275 was identified. The flavonoid, epiafzelechin, was isolated and fully characterized with the concerted use of NMR spectroscopy, circular dichroism, and optical rotation. Electronic circular dichroism and optical rotation TDDFT calculations were also performed, and their agreement with the experimental results confirmed the enantiomeric identity of the isolated natural product. The antioxidant activity of the compound was also investigated.
7-Oxabicyclo[4.1.0]heptan-2-ol, 4,4,6-trimethyl-
Aluminum hydride oxide
Aluminum,(N,N-dimethylmethanamine)trihydro-, (T-4)-
PREGN-4-ENE-3,20-DIOL
Hydrogen cation
Dodecanethiol (8CI,9CI)
1-[(3s,8s,9s,10r,13s,14s,17s)-3-hydroxy-10,13-dimethyl-2,3,6,7,8, 9,11,12,14,15,16,17-dodecahydro-1h-cyclopenta[a]phenanthren-17-yl ]ethanone
Retinal
Benzenesulfonamide,N-(5-methyl-3-isoxazolyl)-4-nitroso-
4-Nitro Sulfamethoxazole