Superstructures with cyclodextrins: Chemistry and applications III

  1. editorImage
  1. Editors: Prof. Gerhard Wenz, Univerität des Saarlandes
    Prof. Eric Monflier, Université d'Artois

Cyclodextrins (CDs) are of increasing scientific and commercial interest because they are readily available, harmless and well-defined, forming sophisticated supramolecular structures in aqueous media. More than 2,300 publications and more than 1,200 patents appeared in 2015 in which CDs played a significant role. CD chemistry has developed into a very attractive field of research. This series follows "Superstructures with cyclodextrins: Chemistry and applications II" and "Superstructures with cyclodextrins: Chemistry and applications".

  • Editorial
  • Published 10 May 2016

Beilstein J. Org. Chem. 2016, 12, 937–938, doi:10.3762/bjoc.12.91

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  • Published 02 Sep 2015

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Beilstein J. Org. Chem. 2015, 11, 1530–1540, doi:10.3762/bjoc.11.168

Cholesterol lowering effects of mono-lactose-appended β-cyclodextrin in Niemann–Pick type C disease-like HepG2 cells

  1. Keiichi Motoyama,
  2. Yumi Hirai,
  3. Rena Nishiyama,
  4. Yuki Maeda,
  5. Taishi Higashi,
  6. Yoichi Ishitsuka,
  7. Yuki Kondo,
  8. Tetsumi Irie,
  9. Takumi Era and
  10. Hidetoshi Arima
  • Full Research Paper
  • Published 03 Nov 2015

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Beilstein J. Org. Chem. 2015, 11, 2079–2086, doi:10.3762/bjoc.11.224

Synthesis, structure, and mechanical properties of silica nanocomposite polyrotaxane gels

  1. Kazuaki Kato,
  2. Daisuke Matsui,
  3. Koichi Mayumi and
  4. Kohzo Ito
  • Full Research Paper
  • Published 16 Nov 2015

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Beilstein J. Org. Chem. 2015, 11, 2194–2201, doi:10.3762/bjoc.11.238

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  • Published 23 Nov 2015

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Beilstein J. Org. Chem. 2015, 11, 2267–2277, doi:10.3762/bjoc.11.247

Co-solvation effect on the binding mode of the α-mangostin/β-cyclodextrin inclusion complex

  1. Chompoonut Rungnim,
  2. Sarunya Phunpee,
  3. Manaschai Kunaseth,
  4. Supawadee Namuangruk,
  5. Kanin Rungsardthong,
  6. Thanyada Rungrotmongkol and
  7. Uracha Ruktanonchai
  • Full Research Paper
  • Published 25 Nov 2015

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Beilstein J. Org. Chem. 2015, 11, 2306–2317, doi:10.3762/bjoc.11.251

Preparation of Pickering emulsions through interfacial adsorption by soft cyclodextrin nanogels

  1. Shintaro Kawano,
  2. Toshiyuki Kida,
  3. Mitsuru Akashi,
  4. Hirofumi Sato,
  5. Motohiro Shizuma and
  6. Daisuke Ono
  • Full Research Paper
  • Published 30 Nov 2015

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Beilstein J. Org. Chem. 2015, 11, 2355–2364, doi:10.3762/bjoc.11.257

Size-controlled and redox-responsive supramolecular nanoparticles

  1. Raquel Mejia-Ariza,
  2. Gavin A. Kronig and
  3. Jurriaan Huskens
  • Full Research Paper
  • Published 01 Dec 2015

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Beilstein J. Org. Chem. 2015, 11, 2388–2399, doi:10.3762/bjoc.11.260

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  • Published 07 Dec 2015

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Beilstein J. Org. Chem. 2015, 11, 2459–2473, doi:10.3762/bjoc.11.267

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  • Published 16 Dec 2015

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Beilstein J. Org. Chem. 2015, 11, 2616–2630, doi:10.3762/bjoc.11.281

Synthesis and photophysical characteristics of polyfluorene polyrotaxanes

  1. Aurica Farcas,
  2. Giulia Tregnago,
  3. Ana-Maria Resmerita,
  4. Pierre-Henri Aubert and
  5. Franco Cacialli
  • Full Research Paper
  • Published 21 Dec 2015

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Beilstein J. Org. Chem. 2015, 11, 2677–2688, doi:10.3762/bjoc.11.288

Physical properties and biological activities of hesperetin and naringenin in complex with methylated β-cyclodextrin

  1. Waratchada Sangpheak,
  2. Jintawee Kicuntod,
  3. Roswitha Schuster,
  4. Thanyada Rungrotmongkol,
  5. Peter Wolschann,
  6. Nawee Kungwan,
  7. Helmut Viernstein,
  8. Monika Mueller and
  9. Piamsook Pongsawasdi
  • Full Research Paper
  • Published 29 Dec 2015

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Beilstein J. Org. Chem. 2015, 11, 2763–2773, doi:10.3762/bjoc.11.297

Polydisperse methyl β-cyclodextrin–epichlorohydrin polymers: variable contact time 13C CP-MAS solid-state NMR characterization

  1. Isabelle Mallard,
  2. Davy Baudelet,
  3. Franca Castiglione,
  4. Monica Ferro,
  5. Walter Panzeri,
  6. Enzio Ragg and
  7. Andrea Mele
  • Full Research Paper
  • Published 30 Dec 2015

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Beilstein J. Org. Chem. 2015, 11, 2785–2794, doi:10.3762/bjoc.11.299

Determination of formation constants and structural characterization of cyclodextrin inclusion complexes with two phenolic isomers: carvacrol and thymol

  1. Miriana Kfoury,
  2. David Landy,
  3. Steven Ruellan,
  4. Lizette Auezova,
  5. Hélène Greige-Gerges and
  6. Sophie Fourmentin
  • Full Research Paper
  • Published 08 Jan 2016

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Beilstein J. Org. Chem. 2016, 12, 29–42, doi:10.3762/bjoc.12.5

Supramolecular polymer assembly in aqueous solution arising from cyclodextrin host–guest complexation

  1. Jie Wang,
  2. Zhiqiang Qiu,
  3. Yiming Wang,
  4. Li Li,
  5. Xuhong Guo,
  6. Duc-Truc Pham,
  7. Stephen F. Lincoln and
  8. Robert K. Prud’homme
  • Review
  • Published 12 Jan 2016

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Beilstein J. Org. Chem. 2016, 12, 50–72, doi:10.3762/bjoc.12.7

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  • Published 14 Jan 2016

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Beilstein J. Org. Chem. 2016, 12, 73–80, doi:10.3762/bjoc.12.8

Supramolecular structures based on regioisomers of cinnamyl-α-cyclodextrins – new media for capillary separation techniques

  1. Gabor Benkovics,
  2. Ondrej Hodek,
  3. Martina Havlikova,
  4. Zuzana Bosakova,
  5. Pavel Coufal,
  6. Milo Malanga,
  7. Eva Fenyvesi,
  8. Andras Darcsi,
  9. Szabolcs Beni and
  10. Jindrich Jindrich
  • Full Research Paper
  • Published 19 Jan 2016

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Beilstein J. Org. Chem. 2016, 12, 97–109, doi:10.3762/bjoc.12.11

Thermal and oxidative stability of Atlantic salmon oil (Salmo salar L.) and complexation with β-cyclodextrin

  1. Daniel I. Hădărugă,
  2. Mustafa Ünlüsayin,
  3. Alexandra T. Gruia,
  4. Cristina Birău (Mitroi),
  5. Gerlinde Rusu and
  6. Nicoleta G. Hădărugă
  • Full Research Paper
  • Published 02 Feb 2016

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Beilstein J. Org. Chem. 2016, 12, 179–191, doi:10.3762/bjoc.12.20

Interactions of cyclodextrins and their derivatives with toxic organophosphorus compounds

  1. Sophie Letort,
  2. Sébastien Balieu,
  3. William Erb,
  4. Géraldine Gouhier and
  5. François Estour
  • Review
  • Published 05 Feb 2016

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Beilstein J. Org. Chem. 2016, 12, 204–228, doi:10.3762/bjoc.12.23

Enabling technologies and green processes in cyclodextrin chemistry

  1. Giancarlo Cravotto,
  2. Marina Caporaso,
  3. Laszlo Jicsinszky and
  4. Katia Martina
  • Review
  • Published 15 Feb 2016

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Beilstein J. Org. Chem. 2016, 12, 278–294, doi:10.3762/bjoc.12.30

Optimized methods for preparation of 6I-(ω-sulfanyl-alkylene-sulfanyl)-β-cyclodextrin derivatives

  1. Eva Bednářová,
  2. Simona Hybelbauerová and
  3. Jindřich Jindřich
  • Full Research Paper
  • Published 24 Feb 2016

Beilstein J. Org. Chem. 2016, 12, 349–352, doi:10.3762/bjoc.12.38

New synthetic strategies for xanthene-dye-appended cyclodextrins

  1. Milo Malanga,
  2. Andras Darcsi,
  3. Mihaly Balint,
  4. Gabor Benkovics,
  5. Tamas Sohajda and
  6. Szabolcs Beni
  • Full Research Paper
  • Published 17 Mar 2016

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Beilstein J. Org. Chem. 2016, 12, 537–548, doi:10.3762/bjoc.12.53

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  • Published 21 Mar 2016

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Beilstein J. Org. Chem. 2016, 12, 549–563, doi:10.3762/bjoc.12.54

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