Recovery of β-cyclodextrin and quick quantitative determination of organic compounds from aqueous system

Huanan Ligong Daxue Xuebao/Journal of South China University of Technology (Natural Science)

Volumn 35, Issue 4, 2007, Pages 1-5

  Ji, Hong Bing ^a   Shi, Dong Po ^a   Hu, Xiao Fang ^a   Pei, Li Xia ^a   Li, Zhong ^a  

^a SOUTH CHINA UNIVERSITY OF TECHNOLOGY   (China)

Author keywords

cyclodextrin; Inclusion; Quantitative determination; Recovery

Indexed keywords

ACETONE; ALCOHOLS; INCLUSIONS; ORGANIC COMPOUNDS; ORGANIC SOLVENTS; SOLVENT EXTRACTION; WATER;

AQUEOUS REACTION SYSTEM; BENZALDEHYDE; BENZYL ALCOHOL; QUANTITATIVE DETERMINATION;

CYCLODEXTRINS;

EID: 34347229728     PISSN: 1000565X     EISSN: None     Source Type: Journal    
DOI: None     Document Type: Article

References (14)

1. Bender M L, Komiyama M. Cyclodextrin chemistry[M]. New York: Springer-Verlag, 1978.
2. Reddy L R, Reddy M A, Bhanumathi N, et al. An efficient method for cleavage of epoxides with aromatic amines catalysed by β-cyclodextrin in water[J]. Synlett, 2000 (3): 339-340.
3. Reddy M A, Bhanumathi N, Rao K R. Asymmetric synthesis of 2-azido-1-arylethanols from azido aryl ketone-β-cyclodextrin complexes and sodium borohydride in water[J]. Chem Commun, 2001(19): 1974-1975.
4. Krishnaveni N S, Surendra K, Reddy M A, et al. Highly efficient deprotection of aromatic acetals under neutral conditions using β-cyclodextrin in water[J]. J Org Chem, 2003, 68(5): 2018-2019.
5. Narender M, Reddy M S, Sridhar R, et al. Aqueous phase synthesis of thiazoles and aminothiazoles in the presence of β-cyclodextrin[J]. Tetrahedron Lett, 2005, 46(35): 5953-5955.
6. Reddy A S, Narender M, Rao K R. A new asymmetric synthetic route to substituted piperidines[J]. Tetrahedron, 2007, 63(2): 31-336.
7. Ji H B. Highly shape-selective, biomimetic, and efficient deprotection of carbonyl compounds masked as ethylene acetals or dioxolanes produced from 1, 2-ethanediol[J]. Eur J Org Chem, 2003(18): 3659-3662.
8. Ji H B, Shi D P, Shao M, et al. Transition metal-free and substrate-selective oxidation of alcohols using water as an only solvent in the presence of β-cyclodextrin[J]. Tetrahedron Lett, 2005, 46(14): 2517-2520.
9. Ji H B, Hu X F, Shi D P, et al. Controllable oxidation of sulfides to sulfoxides and sulfones with aqueous hydrogen peroxide in the presence of β-cyclodextrin[J]. Russian J Org Chem, 2006, 42(7): 959-961.
10. Reddy M A, Reddy L R, Bhanumathi N, et al. Selective deprotection of tetrahydropyranyl ethers catalysed by β-cyclodextrin in water[J]. New J Chem, 2001, 25(3): 359-360.
11. Linert W, Margl P, Renz F. Solute-solvent interactions between cyclodextrin and water: A molecular mechanical study[J]. Chem Phys, 1992, 161: 327-330.
12. Gao Qun-yu, Huang Li-xin, Li Wen-de, et al. A study on encapsulation technology and the releasing law of vanillin inclusion complexes[J]. Journal of South China University of Technology: Natural Science Edition, 2000, 28(7): 15-19.