DR ANTHONY MELVIN CRASTO,WorldDrugTracker, helping millions, A 90 % paralysed man in action for you, I am suffering from transverse mylitis and bound to a wheel chair, With death on the horizon, nothing will not stop me except God................DR ANTHONY MELVIN CRASTO Ph.D ( ICT, Mumbai) , INDIA 25Yrs Exp. in the feld of Organic Chemistry,Working for GLENMARK GENERICS at Navi Mumbai, INDIA. Serving chemists around the world. Helping them with websites on Chemistry.Million hits on google, world acclamation from industry, academia, drug authorities for websites, blogs and educational contribution

Monday 12 January 2015

Novel 1,3-Dipolar Cycloadditions of Cyclobutene Diester Epoxides to Polycyclic Aromatic Hydrocarbons

http://www.mdpi.org/ecsoc/ecsoc-7/papers/a009/a009.htm

Novel 1,3-Dipolar Cycloadditions of Cyclobutene Diester Epoxides to Polycyclic Aromatic Hydrocarbons [1]


Davor Margetiæ,*A Ronald N. WarrenerB and Douglas N. ButlerB
A Laboratory for Physical Organic Chemistry,
Department of Organic Chemistry and Biochemistry,
Ruðer Boškoviæ Institute, Bijenièka c. 54, 10000 Zagreb, Croatia
(*) Corresponding author. Email: margetid@emma.irb.hr
B Centre for Molecular Architecture,
Central Queensland University, Rockhampton, Queensland, 4702, Australia









http://www.mdpi.org/ecsoc/ecsoc-7/papers/a009/a009.htm




























Zagreb is the capital of Croatia and one of the must-see places in Croatia. It has a population of roughly 800,000 people and it is a transportation hub ...





http://croatia-wave.com/locations/info/zagreb




Old town and cathedral from Gradec in Zagreb, Croatia





Trg Bana Jelacica Square Zagreb, Croatia





http://www.travelpulse.com/news/hotels-and-resorts/doubletree-by-hilton-zagreb-to-open-next-year-in-croatia.html

DRUG APPROVALS BY DR ANTHONY MELVIN CRASTO .....FOR BLOG HOME CLICK HERE

Join me on Linkedin

View Anthony Melvin Crasto Ph.D's profile on LinkedIn

Join me on Facebook FACEBOOK
Join me on twitterFollow amcrasto on Twitter     
Join me on google plus Googleplus

 amcrasto@gmail.com


Rubiothiazepine a Novel Unusual Cytotoxic Alkaloid from Ixora undulata Roxb. Leaves

 

compound (1) is 7-[(β-D-glucopyranosyl)oxy]-6- hydroxy-2-methoxy-6,7-dihydro-1,3-thiazepine and trivially named as `Rubiothiazepine` (Structure I).
 

Citation: Mohammed MMD, Ibrahim NA, Chen M, Zhai L (2014) Rubiothiazepine a Novel Unusual Cytotoxic Alkaloid from Ixora undulata Roxb. Leaves. Nat Prod Chem Res 2:128 doi: 10.4172/2329-6836.1000128

http://esciencecentral.org/journals/rubiothiazepine-a-novel-unusual-cytotoxic-alkaloid-from-ixora-undulata-roxb-leaves-2329-6836.1000128.php?aid=24194
Magdy M. D. Mohammed1,2*, Nabaweya A Ibrahim2, Ming Chen3 and Lin Zhai3
1Danish Institute of Agricultural Sciences, Department of Food Science, Research Center Aarslev, Kirstinebjergvej 10, DK-5792 Aarslev, Denmark
2Pharmacognosy Department, National Research Center, Dokki-12311, Cairo, Egypt
3Department of Clinical Microbiology, University Hospital of Copenhagen (Rigshospitalet), Tagensvej 20, DK-2200 Copenhagen N, Denmark
Corresponding Author : Magdy Mostafa Desoky Mohammed
Danish Institute of Agricultural Sciences
Department of Food Science, Research Center Aarslev
Kirstinebjergvej 10, DK-5792 Aarslev, Denmark
Tel: 00201022610332
E-mail: melhenawy111@gmail.com

 
Magdy M. D. Mohammed
Assistant Professor of Chemistry of Medicinal and Aromatic Plants, Pharmacognosy Department






.............
 
Magdy M. D. Mohammed




Assistant Professor of


Chemistry of Medicinal and Aromatic Plants, Pharmacognosy Department




Dikutip olehTahun
Phytochemical investigation and hepatoprotective activity of Cupressus sempervirens L. leaves growing in Egypt
NA Ibrahim, HR El-Seedi, MMD Mohammed
Natural product research 21 (10), 857-866

162007
Anti-HIV-1 and cytotoxicity of the alkaloids of Erythrina abyssinica Lam. growing in Sudan
MMD Mohammed, NA Ibrahim, NE Awad, AA Matloub, AG Mohamed-Ali, ...
Natural product research 26 (17), 1565-1575

62012
Two new phorbol-type diterpene esters from Synadenium grantii Hook f. leaves
EM Hassan, MMD Mohammed, SM Mohamed
Records of Natural Products 6 (3), 255-262

62012
The cytotoxic activity of Linum grandiflorum leaves
MMD Mohammed, M Chen, L Zhai, NA Ibrahim
European Journal of Chemistry 1 (2), 110-114

62010
New acylated flavone and cyanogenic glycosides from Linum grandiflorum
MMD Mohammed, LP Christensen, NA Ibrahim, NE Awad, IF Zeid, ...
Natural product research 23 (5), 489-497

52009
Constituents and biological activity of the chloroform extract and essential oil of Cupressus sempervirens
NA Ibrahim, HR El-Seedi, MMD Mohammed
Chemistry of natural compounds 45 (3), 309-313

42009
Anti-HIV-1 activities of the extracts from the medicinal plant Linum grandiflorum Desf
MMD Mohammed, LP Christensen, NA Ibrahim, NE Awad, IF Zeid, ...
Med. Aroma. Plant Sci. Biotechnol 3, 37-41

32009
Cytotoxic flavonoids from Diplotaxis harra (Forssk.) Boiss. growing in Sinai
MMD Mohammed, ER El-Sharkawy, AA Matloub
Journal of Medicinal Plants Research 7 (1), 19-23

12013
Anti-HIV-1 and cytotoxicity of the alkaloids of Erythrina abyssinica Lam. growing in Sudan
MM Mohammed, NA Ibrahim, NE Awad, AA Matloub, AG Mohamed-Ali, ...
Erratun in Nat Prod Res 27, 295

12013
Cytotoxic flavonoids from Diplotaxis harra (Forssk.) Boiss. growing in Sinai
M Mohammed, ER El-Sharkawy, AA Matloub
JOURNAL OF MEDICINAL PLANTS RESEARCH 5 (20), 5099-5103

12011
Anti-influenza A virus activity of a new dihydrochalcone diglycoside isolated from the Egyptian seagrass Thalassodendron ciliatum (Forsk.) den Hartog
MMD Mohammed, AHA Hamdy, NM El-Fiky, WSA Mettwally, AA El-Beih, ...
Natural product research 28 (6), 377-382

2014
Isolation and anti-HIV-1 activity of a new sesquiterpene lactone from Calocephalus brownii F. Muell.
MMD Mohammed, LP Christensen, PL Colla
Natural product research 28 (4), 221-229

2014
Rubiothiazepine a Novel Unusual Cytotoxic Alkaloid from Ixora undulata
MMD Mohammed, NA Ibrahim, M Chen, L Zhai
Roxb. Leaves. Nat Prod Chem Res 2 (128), 2

2014
Antiviral and cytotoxic activities of anthraquinones isolated from Cassia roxburghii Linn. leaves
M Mohammed, SS El-Souda, SM El-Hallouty, N Kobayashi
Herba Polonica 59 (4), 33-44

2013
4th World Congress on Bioavailability and Bioequivalence: Pharmaceutical R&D Summit
MMD Mohammed

2013
Chemical composition, antimicrobial activity of the essential oil of the flowers of Paulownia tomentosa (Thunb.) Steud. growing in Egypt.
ES Ibrahim, N.A., El-Hawary, S.S., Magdy M. D. Mohammed, Faraid, M.A ...
Journal of Applied Sciences Research 9 (4), 3228-3232

2013
D-mannitol in ameliorating some metabolic disorders in Schistosomal mansoni infected mice.
MMDM Nagy S. El-Rigal, Sanaa A. Ali, Mohga S. Abd-Allah, El-Sayed M. El ...
Egyptian Pharmaceutical Journal 10 (2), 137–166

2011
POTENTIAL ANTICANCER AGENTS FROM LINUM GRANDIFLORUM LEAVES
M Mohammed, M Chen, L Zhai, NA Ibrahim
ANTICANCER RESEARCH 28 (5 C), 3411-3411





DRUG APPROVALS BY DR ANTHONY MELVIN CRASTO .....FOR BLOG HOME CLICK HERE

Join me on Linkedin

View Anthony Melvin Crasto Ph.D's profile on LinkedIn

Join me on Facebook FACEBOOK
Join me on twitterFollow amcrasto on Twitter     
Join me on google plus Googleplus

 amcrasto@gmail.com






Boric Ester-Type Molten Salt via Dehydrocoupling Reaction


Figure 1. 1H-NMR of 5 (solvent: CDCl3; 10%; r.t.; TMS; 400 MHz).


http://www.mdpi.com/1422-0067/15/11/21080

http://www.mdpi.com/1422-0067/15/11/21080/htm
Ijms 15 21080 g007 1024

Int. J. Mol. Sci. 201415(11), 21080-21089; doi:10.3390/ijms151121080
Article
Boric Ester-Type Molten Salt via Dehydrocoupling Reaction
Noriyoshi Matsumi 1,*, Yoshiyuki Toyota 1, Prerna Joshi 1, Puhup Puneet 1, Raman Vedarajan 1 and Toshihiro Takekawa 2
1School of Materials Science, Japan Advanced Institute of Science and Technology (JAIST), 1-1 Asahidai, Nomi, Ishikawa 923-1292, Japan; E-Mails: brothertobrother@gmail.com (Y.T.); joshi.prerna2011@gmail.com (P.J.); rupakagain2008@gmail.com (P.P.); raman@jaist.ac.jp (R.V.)
2Advanced Materials Laboratory, Nissan Motor Co., Ltd., 1 Natsushima-cho, Yokosuka-shi, Kanagawa 237-8523, Japan; E-Mail: t-takekawa@mail.nissan.co.jp
*Author to whom correspondence should be addressed; E-Mail: matsumi@jaist.ac.jp; Tel.: + 81-761-51-1600; Fax: +81-761-51-1665.


 Prerna J.JOSHI PRERNA




Noriyoshi Matsumi

Ijms 15 21080 g002 1024
Figure 2. 13C-NMR of 5 (solvent: DMSO; r.t.; 100 MHz)

Ijms 15 21080 g003 1024

Figure 3. 11B-NMR of 5 (solvent: CDCl3; r.t.; external standard: B(OCH3); 128 MHz).

Ijms 15 21080 g004 1024

Figure 4. 19F-NMR of 5 (solvent: CDCl3; r.t.; external standard: C6H5CF3; 376 MHz).


data
1H-NMR (CDCl3, δ, ppm) 1.26–2.50 (20H, 9-BBN), 3.98 (3H, CH3), 4.33 (2H, –NCH2CH2O), 5.62 (2H, –NCH2CH2OB–), 7.21, 7.35 (2H, –NCHCHN–), 8.87 (1H, –NCHN–). 

13C-NMR (DMSO-d6, δ, ppm) 23.3–33.2 (9-BBN), 36.1, 52.1, 59.8, 119.4 (q, CF3), 123.1–123.8 (N–C=C–N), 137.3 (N–C=N). 

11B-NMR (CDCl3, δδ, ppm) 33.3.






kanagawa japan















FOOD.















DRUG APPROVALS BY DR ANTHONY MELVIN CRASTO .....FOR BLOG HOME CLICK HERE

Join me on Linkedin

View Anthony Melvin Crasto Ph.D's profile on LinkedIn

Join me on Facebook FACEBOOK
Join me on twitterFollow amcrasto on Twitter     
Join me on google plus Googleplus

 amcrasto@gmail.com






13C NMR of dimethyl 3,4,5,6-tetraphenylphthalate


13C NMR of dimethyl 3,4,5,6-tetraphenylphthalate




enter image description here

he upfield peak at 52.28 is in the expected position for C1, the ester methyl carbon. Down at the other end of the spectrum, the peak at 168.71 is in the expected position for an ester carbonyl carbon (C2).
In the region for aromatic carbons we see 5 low intensity peaks between 143 and 132. These belong to the (unprotonated) quaternary carbons 3, 4, 5, 6, 10. Using diethyl phthalate as a model compound, I would guess that the peak at 132.19 is from C3. The two peaks at 138.73 and 138.60 have the same height and are closely spaced suggesting very similar environments, I might guess them to be C6 and C10, just not sure which is which. Noting that the peak for the carbon corresponding to our C5 is downfield of the peak corresponding to our C4 in the model compound, I would expect the same trend to hold here, just with each of the peaks shifted downfield due to attachment of a phenyl group. So I would assign the peak at 143.27 to C5 and the peak at 139.29 to C4.
This leaves the protonated aromatic carbons for us to consider. The 2 peaks at 125.97 and 126.83 are half the intensity of the other protonated aromatic signals, therefor assign them to C9 and C13 as there are only half as many of these carbons as compared to the other protonated aromatic carbons. It's not clear which peak belongs to C9 and which to C13. This leaves us with the 4 signals due to C7, C8, C11 and C12. , I would expect C7 and C11 to be downfield from C8 and C12. Therefor, I would assign C7 and C11 to the peaks at 129.71 and 130.88, not knowing which is which. C8 and C12 then belong to the signals at 126.88 and 127.41, not knowing which belongs to which.
DRUG APPROVALS BY DR ANTHONY MELVIN CRASTO .....FOR BLOG HOME CLICK HERE

Join me on Linkedin

View Anthony Melvin Crasto Ph.D's profile on LinkedIn

Join me on Facebook FACEBOOK
Join me on twitterFollow amcrasto on Twitter     
Join me on google plus Googleplus

 amcrasto@gmail.com