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Showing results for h sharghi
Search for H Shargi instead (1 results)
3,4-Dimeth-oxy-N-((E)-4-{[1-(prop-2-en-1-yl)-1H-1,2,3-triazol-4-yl]meth-oxy}benzyl-idene)aniline.
Akkurt M, Jarrahpour A, Sharghi H, Chermahini MM, Shiri P, Büyükgüngör O. Akkurt M, et al. Acta Crystallogr Sect E Struct Rep Online. 2012 Jul 1;68(Pt 7):o2127. doi: 10.1107/S1600536812026761. Epub 2012 Jun 16. Acta Crystallogr Sect E Struct Rep Online. 2012. PMID: 22798803 Free PMC article.
In the title compound, C(21)H(22)N(4)O(3), the triazole ring is planar [maximum deviaton = 0.004 (1) A] and makes dihedral angles of 26.21 (8) and 38.66 (8) with the two benzene rings. ...
In the title compound, C(21)H(22)N(4)O(3), the triazole ring is planar [maximum deviaton = 0.004 (1) A] and makes dihedral angles of …
(3R*,4R*)-1-(4-Chloro-phen-yl)-4-[2-hy-droxy-3-(morpholinomethyl)-phen-yl]-3-phen-oxy-azetidin-2-one.
Akkurt M, Jarrahpour A, Sharghi H, Badrabady SA, Büyükgüngör O. Akkurt M, et al. Acta Crystallogr Sect E Struct Rep Online. 2011 Jan 12;67(Pt 2):o325. doi: 10.1107/S1600536811000675. Acta Crystallogr Sect E Struct Rep Online. 2011. PMID: 21523011 Free PMC article.
The beta-lactam ring of the title compound, C(26)H(25)ClN(2)O(4), is nearly planar (r.m.s. deviation = 0.025 A) and the morpholine ring adopts a chair conformation. ...
The beta-lactam ring of the title compound, C(26)H(25)ClN(2)O(4), is nearly planar (r.m.s. deviation = 0.025 A) and the morpholine ri …
2-[(E)-(4-Methyl-phen-yl)imino-meth-yl]-6-(morpholin-4-ylmeth-yl)phenol.
Akkurt M, Türktekin S, Jarrahpour A, Sharghi H, Badrabady SA, Aberi M, Büyükgüngör O. Akkurt M, et al. Acta Crystallogr Sect E Struct Rep Online. 2010 Dec 18;67(Pt 1):o147-8. doi: 10.1107/S1600536810052311. Acta Crystallogr Sect E Struct Rep Online. 2010. PMID: 21522655 Free PMC article.
In the title compound, C(19)H(22)N(2)O(2), the morpholine ring adopts an almost perfect normal chair conformation with puckering parameters Q(T), teta and of 0.5642 (18) A, 177.32 (17) and = 10 (4), respectively. ...
In the title compound, C(19)H(22)N(2)O(2), the morpholine ring adopts an almost perfect normal chair conformation with puckering para …
The GUDMAP database--an online resource for genitourinary research.
Harding SD, Armit C, Armstrong J, Brennan J, Cheng Y, Haggarty B, Houghton D, Lloyd-MacGilp S, Pi X, Roochun Y, Sharghi M, Tindal C, McMahon AP, Gottesman B, Little MH, Georgas K, Aronow BJ, Potter SS, Brunskill EW, Southard-Smith EM, Mendelsohn C, Baldock RA, Davies JA, Davidson D. Harding SD, et al. Development. 2011 Jul;138(13):2845-53. doi: 10.1242/dev.063594. Development. 2011. PMID: 21652655 Free PMC article.
Solvent-free and room temperature synthesis of 3-arylquinolines from different anilines and styrene oxide in the presence of Al(2)O(3)/MeSO(3)H.
Sharghi H, Aberi M, Khataminejad M, Shiri P. Sharghi H, et al. Beilstein J Org Chem. 2017 Sep 20;13:1977-1981. doi: 10.3762/bjoc.13.193. eCollection 2017. Beilstein J Org Chem. 2017. PMID: 29062417 Free PMC article.
A highly efficient, simple and environmentally friendly synthesis of 3-arylquinolines has been developed in the presence of Al(2)O(3)/MeSO(3)H via one-pot reaction of anilines and styrene oxide. This methodology provides very rapid access to 3-arylquinolines in good to exc …
A highly efficient, simple and environmentally friendly synthesis of 3-arylquinolines has been developed in the presence of Al(2)O(3)/MeSO(3 …
MP2, DFT and ab initio calculations on thioxanthone.
Beni AS, Chermahini AN, Sharghi H, Monfared SM. Beni AS, et al. Spectrochim Acta A Mol Biomol Spectrosc. 2011 Nov;82(1):49-55. doi: 10.1016/j.saa.2011.06.059. Epub 2011 Jun 30. Spectrochim Acta A Mol Biomol Spectrosc. 2011. PMID: 21820349
The theoretical electronic absorption spectra have been calculated using CIS method. (13)C and (1)H NMR of the title compound have been calculated by means of B3LYP density functional method with 6-31+G(d,p) basis set. ...
The theoretical electronic absorption spectra have been calculated using CIS method. (13)C and (1)H NMR of the title compound have be …
21 results