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Items: 1 to 20 of 398

1.

Synthesis and characterization of N-aryl chitosan derivatives.

Sajomsang W, Tantayanon S, Tangpasuthadol V, Thatte M, Daly WH.

Int J Biol Macromol. 2008 Aug 15;43(2):79-87. doi: 10.1016/j.ijbiomac.2008.03.010.

PMID:
18514305
2.

Quaternization of N-aryl chitosan derivatives: synthesis, characterization, and antibacterial activity.

Sajomsang W, Tantayanon S, Tangpasuthadol V, Daly WH.

Carbohydr Res. 2009 Dec 14;344(18):2502-11. doi: 10.1016/j.carres.2009.09.004.

PMID:
19863950
3.

Preparation of substituted quaternized arylfuran chitosan derivatives and their antimicrobial activity.

Chethan PD, Vishalakshi B, Sathish L, Ananda K, Poojary B.

Int J Biol Macromol. 2013 Aug;59:158-64. doi: 10.1016/j.ijbiomac.2013.04.045.

PMID:
23608102
4.

Quaternized N-substituted carboxymethyl chitosan derivatives as antimicrobial agents.

Mohamed NA, Sabaa MW, El-Ghandour AH, Abdel-Aziz MM, Abdel-Gawad OF.

Int J Biol Macromol. 2013 Sep;60:156-64. doi: 10.1016/j.ijbiomac.2013.05.022.

PMID:
23732327
5.

Synthesis of novel quaternary chitosan derivatives via N-Chloroacyl-6-O-triphenylmethylchitosans.

Holappa J, Nevalainen T, Soininen P, Másson M, Järvinen T.

Biomacromolecules. 2006 Feb;7(2):407-10.

PMID:
16471908
6.

Synthesis and antimicrobial activity of the Schiff base from chitosan and citral.

Jin X, Wang J, Bai J.

Carbohydr Res. 2009 Apr 21;344(6):825-9. doi: 10.1016/j.carres.2009.01.022.

PMID:
19230865
7.

Synthesis of dehydroabietic acid-modified chitosan and its drug release behavior.

Duan W, Shen C, Fang H, Li GH.

Carbohydr Res. 2009 Jan 5;344(1):9-13. doi: 10.1016/j.carres.2008.08.007.

PMID:
18976985
8.

Synthesis of phosphorylated chitosan by novel method and its characterization.

Jayakumar R, Nagahama H, Furuike T, Tamura H.

Int J Biol Macromol. 2008 May 1;42(4):335-9. doi: 10.1016/j.ijbiomac.2007.12.011.

PMID:
18279950
9.

Synthesis and characterization of a crosslinked chitosan derivative with a complexing agent and its adsorption studies toward metal(II) ions.

Krishnapriya KR, Kandaswamy M.

Carbohydr Res. 2009 Sep 8;344(13):1632-8. doi: 10.1016/j.carres.2009.05.025.

PMID:
19545861
10.

Synthesis and characterization of diethoxy phosphoryl chitosan.

Ma L, Li G, Li L, Liu P.

Int J Biol Macromol. 2010 Nov 1;47(4):578-81. doi: 10.1016/j.ijbiomac.2010.06.014.

PMID:
20620160
11.

Synthesis and properties of photosensitive chitosan derivatives.

Ma G, Qian B, Yang J, Hu C, Nie J.

Int J Biol Macromol. 2010 Jun;46(5):558-61. doi: 10.1016/j.ijbiomac.2010.02.009.

PMID:
20219529
12.

Novel chitosan-derived nanomaterials and their micelle-forming properties.

Zhang C, Ding Y, Ping Q, Yu LL.

J Agric Food Chem. 2006 Nov 1;54(22):8409-16.

PMID:
17061814
13.

Synthesis of new bis-1,2,4-triazole derivatives.

Bekircan O, Bektas H.

Molecules. 2006 Jun 21;11(6):469-77.

14.
15.

Antibacterial activity of quaternary ammonium chitosan containing mono or disaccharide moieties: preparation and characterization.

Sajomsang W, Gonil P, Tantayanon S.

Int J Biol Macromol. 2009 Jun 1;44(5):419-27. doi: 10.1016/j.ijbiomac.2009.03.003.

PMID:
19428476
16.

Spectroscopic study of molecular structures of novel Schiff base derived from o-phthaldehyde and 2-aminophenol and its coordination compounds together with their biological activity.

Abdallah SM, Mohamed GG, Zayed MA, Abou El-Ela MS.

Spectrochim Acta A Mol Biomol Spectrosc. 2009 Sep 1;73(5):833-40. doi: 10.1016/j.saa.2009.04.005.

PMID:
19505840
17.
18.

Advances on selective C-6 oxidation of chitosan by TEMPO.

Bordenave N, Grelier S, Coma V.

Biomacromolecules. 2008 Sep;9(9):2377-82. doi: 10.1021/bm800375v.

PMID:
18700797
19.

Chitosan-graft poly(p-dioxanone) copolymers: preparation, characterization, and properties.

Wang XL, Huang Y, Zhu J, Pan YB, He R, Wang YZ.

Carbohydr Res. 2009 Apr 21;344(6):801-7. doi: 10.1016/j.carres.2009.02.009.

PMID:
19268919
20.

Synthesis and spectroscopic properties of novel asymmetric Schiff bases.

Güngör O, Gürkan P.

Spectrochim Acta A Mol Biomol Spectrosc. 2010 Sep 15;77(1):304-11. doi: 10.1016/j.saa.2010.05.027.

PMID:
20541456

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