scholarly journals Correction to Simple Chiral Derivatization Protocols for 1H NMR and 19F NMR Spectroscopic Analysis of the Enantiopurity of Chiral Diols

2019 ◽  
Vol 84 (14) ◽  
pp. 9395-9396
Author(s):  
Sonia Lozano Yeste ◽  
Magdalena E. Powell ◽  
Steven D. Bull ◽  
Tony D. James
2002 ◽  
Vol 27 (1-2) ◽  
pp. 191-200 ◽  
Author(s):  
Eva Lenz ◽  
Steve Taylor ◽  
Craig Collins ◽  
Ian D Wilson ◽  
Dave Louden ◽  
...  

2009 ◽  
Vol 50 (8) ◽  
pp. 876-879 ◽  
Author(s):  
Magdalena E. Powell ◽  
Andrew M. Kelly ◽  
Steven D. Bull ◽  
Tony D. James

1994 ◽  
Vol 51 (3) ◽  
pp. 157-166
Author(s):  
Akira MITUI ◽  
Akihiro KANAYAMA ◽  
Shigeki TAKAYAMA ◽  
Kunihiko TAKEDA

2019 ◽  
Vol 3 (2) ◽  
pp. 102
Author(s):  
Mulyadi Tanjung ◽  
Devina Oktari Rahayu ◽  
Tjitjik Srie Tjahjandarie

AbstrakToddalia asiatica merupakan tumbuhan perdu yang tersebar di Afrika, Asia, Madagascar, dan Australia (Hu et al., 2015). Senyawa metabolit sekunder yang ditemukan tumbuhan Toddalia asiatica L. adalah alkaloid. Ekstraksi senyawa alkaloid dari tumbuhan Toddalia asiatica L. dengan cara maserasi menggunakan pelarut metanol pada suhu kamar. Proses isolasi dilakukan melalui fraksinasi dan pemurnian menggunakan kromatografi kolom gravitasi, dan kromatografi radial. Hasil isolasi yang didapatkan merupakan senyawa alkaloid turunan furokuinolin yaitu skimmianin. Struktur senyawa alkaloid turunan furokuinolin yang  diketahui melalui analisa hasil spektroskopi UV, IR, 1D NMR (1H-NMR dan 13C-NMR),  serta 2D NMR (HMBC dan HMQC) dan uji aktivitas antikanker terhadap sel kanker murin leukemia P-388. Kata kunci : Alkaloid turunan furokuinolin, skimmianin, Toddalia asiatica L., antikanker AbstractToddalia asiatica L. is a bushy plant that spreads in Africa, Asia, Madagascar, and Australia (Hu et al., 2015). The secondary metabolite compound found in Toddalia asiatica L. is alkaloid. Extraction of alkaloid compounds from Toddalia asiatica L. by maceration using methanol at room temperature. The isolation process is diluted by fractionation and purification using column chromatography of gravity and radial chromatography. The result  of isolation is an alkaloid compound derived furokuinolin, skimmianin. The structure of alkaloid compounds derived from furokuinolin known through spectroscopic analysis including UV, IR, 1D NMR (1H-NMR and 13C-NMR), and 2D NMR (HMBC and HMQC) and the anticancer activity test against the cancer cells murine P-388.Key word :    Alkaloid  compound  derived  furokuinolin,  skimmianin,  Toddalia asiatica L., anticancer


2020 ◽  
Vol 22 (35) ◽  
pp. 19969-19974
Author(s):  
Natalia A. Chumakova ◽  
Yaroslav V. Tkachev ◽  
Andrey Kh. Vorobiev ◽  
Anastasya T. Rebrikova ◽  
Mikhail V. Korobov

A combination of 19F and 1H NMR with the Carr–Purcell–Meiboom–Gill (CPMG) pulse sequence was used to examine the mobility of liquids in the interplane space of graphite oxide (GO) for the first time.


2012 ◽  
Vol 36 (1) ◽  
pp. 13-17
Author(s):  
Md Harun Or Rashid ◽  
Md Abdul Gafur ◽  
Md Moklesur Rahman Sarker ◽  
Nurul Karim

Chromatographic purification and spectroscopic analysis of the constituents from the stem  extract of Ipomoea turpethum L. reported 22, 23-dihydro-?-spinasteryl-?-D glucoside (H-1) in  addition to salicylic acid and N-p-comaryltyramine. The structures were elucidated by  spectroscopic analysis including 1H-NMR and 13C-NMR, 1H-1H COSY, 1H-13C COSY, HMQC,  HMBC, UV and IR spectroscopy. 22, 23-dihydro-?-spinasteryl-?-D-glucoside is first reported  from Ipomoea turpethum. DOI: http://dx.doi.org/10.3329/jbas.v36i1.10906 Journal of Bangladesh Academy of Sciences, Vol. 36, No. 1, 13-17, 2012


2018 ◽  
Vol 69 (2) ◽  
pp. 249 ◽  
Author(s):  
X. Y. Jiang ◽  
C. Li ◽  
Q. Q. Chen ◽  
X. C. Weng

This paper reports the comparison of determination methods for extra virgin olive oil (EVOO) adulteration with two kinds of oils, refined olive oil (ROO) and soybean oil by 19FNMR, 1H NMR and chemical titration. The determination of adulteration of EVOO with ROO by 19F NMR was comparable to the conventional method. The contents of oleic, linoleic and linolenic acids of different oil samples can be determined by both 1H NMR and GC-MS. The results obtained from the two methods showed little differences. The adulteration of EVOO with soybean oil is detected by 1H NMR, although the limit of detection of the adulteration level is not less than 4.5%. The research demonstrates that 19F NMR can be a fast and convenient method to detect EVOO if it is adulterated with ROO and 1H NMR can be a fast and convenient method to detect EVOO if it is adulterated with seed oils.


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