These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.
143 related articles for article (PubMed ID: 21244066)
1. Single-hole hollow nanospheres from enantioselective self-assembly of chiral AIE carboxylic acid and amine. Li DM; Zheng YS J Org Chem; 2011 Feb; 76(4):1100-8. PubMed ID: 21244066 [TBL] [Abstract][Full Text] [Related]
2. Highly enantioselective recognition of a wide range of carboxylic acids based on enantioselectively aggregation-induced emission. Li DM; Zheng YS Chem Commun (Camb); 2011 Sep; 47(36):10139-41. PubMed ID: 21833382 [TBL] [Abstract][Full Text] [Related]
3. Enantiomer analysis of chiral carboxylic acids by AIE molecules bearing optically pure aminol groups. Zheng YS; Hu YJ; Li DM; Chen YC Talanta; 2010 Jan; 80(3):1470-4. PubMed ID: 20006116 [TBL] [Abstract][Full Text] [Related]
4. Enantioselective self-assembly of chiral calix[4]arene acid with amines. Zheng YS; Ran SY; Hu YJ; Liu XX Chem Commun (Camb); 2009 Mar; (9):1121-3. PubMed ID: 19225656 [TBL] [Abstract][Full Text] [Related]
5. Enantioselective recognition of α-hydroxycarboxylic acids and N-Boc-amino acids by counterion-displacement assays with a chiral nickel(II) complex. He X; Zhang Q; Wang W; Lin L; Liu X; Feng X Org Lett; 2011 Feb; 13(4):804-7. PubMed ID: 21247141 [TBL] [Abstract][Full Text] [Related]
6. Fluorometric sensing of biogenic amines with aggregation-induced emission-active tetraphenylethenes. Nakamura M; Sanji T; Tanaka M Chemistry; 2011 May; 17(19):5344-9. PubMed ID: 21438041 [TBL] [Abstract][Full Text] [Related]
7. Synthesis of hollow CaCO3 nanospheres templated by micelles of poly(styrene-b-acrylic acid-b-ethylene glycol) in aqueous solutions. Bastakoti BP; Guragain S; Yokoyama Y; Yusa S; Nakashima K Langmuir; 2011 Jan; 27(1):379-84. PubMed ID: 21117696 [TBL] [Abstract][Full Text] [Related]
8. Chirally functionalized hollow nanospheres containing L-prolinamide: synthesis and asymmetric catalysis. Gao J; Liu J; Tang J; Jiang D; Li B; Yang Q Chemistry; 2010 Jul; 16(26):7852-8. PubMed ID: 20509127 [TBL] [Abstract][Full Text] [Related]
9. Preparation of a spontaneous resolution chiral fluorescent system using 2-anthracenecarboxylic acid. Imai Y; Kamon K; Murata K; Harada T; Nakano Y; Sato T; Fujiki M; Kuroda R; Matsubara Y Org Biomol Chem; 2008 Oct; 6(19):3471-5. PubMed ID: 19082147 [TBL] [Abstract][Full Text] [Related]
10. Synthesis of chiral calix[4]arenes bearing aminonaphthol moieties and their use in the enantiomeric recognition of carboxylic acids. Durmaz M; Yilmaz M; Sirit A Org Biomol Chem; 2011 Jan; 9(2):571-80. PubMed ID: 21063630 [TBL] [Abstract][Full Text] [Related]
11. A versatile and practical solvating agent for enantioselective recognition and NMR analysis of protected amines. Iwaniuk DP; Wolf C J Org Chem; 2010 Oct; 75(19):6724-7. PubMed ID: 20822120 [TBL] [Abstract][Full Text] [Related]
12. C-hexaphenyl-substituted trianglamine as a chiral solvating agent for carboxylic acids. Gualandi A; Grilli S; Savoia D; Kwit M; Gawroński J Org Biomol Chem; 2011 Jun; 9(11):4234-41. PubMed ID: 21499627 [TBL] [Abstract][Full Text] [Related]
13. Self-assembly of poly(o-methoxyaniline) hollow nanospheres from a polymeric acid solution. Sui J; Zhang L; Peng H; Travas-Sejdic J; Kilmartin PA Nanotechnology; 2009 Oct; 20(41):415606. PubMed ID: 19762947 [TBL] [Abstract][Full Text] [Related]
14. Synthesis of raspberry-like monodisperse magnetic hollow hybrid nanospheres by coating polystyrene template with Fe(3)O(4)@SiO(2) particles. Wang C; Yan J; Cui X; Wang H J Colloid Interface Sci; 2011 Feb; 354(1):94-9. PubMed ID: 21044785 [TBL] [Abstract][Full Text] [Related]
15. Facile route to synthesize polyurethane hollow microspheres with size-tunable single holes. Li M; Xue J Langmuir; 2011 Apr; 27(7):3229-32. PubMed ID: 21341811 [TBL] [Abstract][Full Text] [Related]
16. Ligand-assisted fabrication of hollow CdSe nanospheres via Ostwald ripening and their microwave absorption properties. Cao M; Lian H; Hu C Nanoscale; 2010 Dec; 2(12):2619-23. PubMed ID: 20967389 [TBL] [Abstract][Full Text] [Related]
17. Highly enantioselective synthesis of gamma-nitro heteroaromatic ketones in a doubly stereocontrolled manner catalyzed by bifunctional thiourea catalysts based on dehydroabietic amine: a doubly stereocontrolled approach to pyrrolidine carboxylic acids. Jiang X; Zhang Y; Chan AS; Wang R Org Lett; 2009 Jan; 11(1):153-6. PubMed ID: 19067569 [TBL] [Abstract][Full Text] [Related]
18. Absolute stereochemical determination of chiral carboxylates using an achiral molecular tweezer. Yoon H; Lee CH; Jang WD Chemistry; 2012 Sep; 18(39):12479-86. PubMed ID: 22907920 [TBL] [Abstract][Full Text] [Related]
19. Hollow-shell-structured nanospheres: a recoverable heterogeneous catalyst for rhodium-catalyzed tandem reduction/lactonization of ethyl 2-acylarylcarboxylates to chiral phthalides. Liu R; Jin R; An J; Zhao Q; Cheng T; Liu G Chem Asian J; 2014 May; 9(5):1388-94. PubMed ID: 24623451 [TBL] [Abstract][Full Text] [Related]
20. Starburst triarylamine donor-acceptor-donor quadrupolar derivatives based on cyano-substituted diphenylaminestyrylbenzene: tunable aggregation-induced emission colors and large two-photon absorption cross sections. Wang B; Wang Y; Hua J; Jiang Y; Huang J; Qian S; Tian H Chemistry; 2011 Feb; 17(9):2647-55. PubMed ID: 21264969 [TBL] [Abstract][Full Text] [Related] [Next] [New Search]