75
Cramer F, Hettler H (1967) Inclusion compounds of cyclodextrins. Naturwissenschaften
54:625–632
Cramer F, Kampe W (1962) Katalyse der decarboxylierung durch cyclodextrine. Eine modellreaktion fur die wirkungsweise der enzyme. Tetrahedron Lett 8:353–356
Cramer F, Kampe W (1965) Inclusion compounds. 17. Catalysis of decarboxylation by cyclodextrins. A model reaction for mechanism of enzymes. J Am Chem Soc 87:1115–1118
Cramer F, Steinle D (1955) Die wirkungsweise der amylase aus Bacillus macerans. Ann Chem
Justus Liebig 595:81–100
Cramer F, Saenger W, Spatz HC (1967) Inclusion compounds. XIX. The formation of inclusion
compounds of α-cyclodextrin in aqueous solutions. Thermodynamics and kinetics. J Am Chem
Soc 89:14–20
Cramer F, MacKensen G, Sensse K (1969) Über einschlussverbindungen, XX ORD-spektren und
konformation der glucose-einheiten in cyclodextrin. Chem Ber 102:494–508
Crini G (2005) Recent developments in polysaccharide-based materials used as adsorbents in wastewater treatment. Prog Polym Sci 30:38–70. https://doi.org/10.1016/j.progpolymsci.2004.11.002
Crini G (2014) Review: a history of cyclodextrins. Chem Rev 114:10940–10975. https://doi.
org/10.1021/cr500081p
Crini G, Morcellet M (2002) Synthesis and applications of adsorbents containing cyclodextrins.
J Sep Sci 25:789–813. https://doi.org/10.1002/1615-9314(20020901)25:13%3c789:AIDJSSC789%3e3.0.CO;2-J
Crini G, Fourmentin S, Fenyvesi É, Torri G, Fourmentin M, Morin-Crini N (2018) Cyclodextrins,
from molecules to applications. Environ Chem Lett 16:1361–1375. https://doi.org/0.1007/
s10311-018-0763-2
Croft AP, Bartsch RA (1983) Synthesis of chemically modified cyclodextrins. Tetrahedron
9:1417–1474
Cserhati T, Dobrovolszky A, Fenyvesi E, Szejtli J (1983) Beta-cyclodextrin polymer beads as GC
packings. J High Resoult Chromatogr 6:442–443
Cutrone G, Benkovics G, Malanga M, Casas-Solvas JM, Fenyvesi É, Sortino S, García-Fuentes
L, Vargas-Berenguel A (2018) Mannoside and 1,2-mannobioside β-cyclodextrin-scaffolded
NO-photodonors for targeting antibiotic resistant bacteria. Carbohydr Polym 199:649–660.
https://doi.org/10.1016/j.carbpol.2018.07.018
Davis ME, Brewster ME (2004) Cyclodextrin-based pharmaceutics: past, present and future. Natl
Rev 3:1023–1035. https://doi.org/10.1038/nrd1576
Demarco PV, Thakkar AL (1970) Cyclohepta-amylose inclusion complexes. A proton magnetic
resonance study. J Chem Soc Chem Commun 1:2–4. https://doi.org/10.1039/C29700000002
Dietrich HV, Cramer F (1954) Über Einschlussverbindungen, VII. Mitteilung, zür struktur der
jodketten in kanal-einschlussverbindungen. Chem Ber 87:806–817
Dong RJ, Zhou YF, Huang XH, Zhu XY, Lu YF, Shen J (2015) Functional supramolecular polymers
for biomedical applications. Adv Mater 27:498–526. https://doi.org/10.1002/adma.201402975
Duchêne D (1987) Cyclodextrins and their industrial uses. Éditions de Santé, Paris
Duchêne D (1991) New trends in cyclodextrins and derivatives. Éditions de Santé, Paris
Duchêne D, Wouessidjewe D (1990a) The current state of beta-cyclodextrin in pharmaceutics. Int
J Drug Formul Biopharm 36:1–6
Duchêne D, Wouessidjewe D (1990b) Pharmaceutical uses of cyclodextrins and derivatives. Drug
Dev Ind Pharm 16:2487–2499. https://doi.org/10.3109/03639049009058543
Duchêne D, Wouessidjewe D (1992) Industrial uses of cyclodextrins and their derivatives. J Coord
Chem 27:223–236. https://doi.org/10.1080/00958979209407955
Duchêne D, Ponchel G, Wouessidjewe D (1992) Cyclodextrins in targeting – application to nanoparticles. Adv Drug Deliv Rev 36:29–40. https://doi.org/10.1016/S0169-409X(98)00053-2
Duchêne D, Bochot A, Loftsson T (2009) Cyclodextrins and their use in pharmacy and cosmetology. STP Pharm Pratiques 19:15–27
Egele K, Samaddar S, Schneider N, Thompson D, Wenz G (2019) Synthesis of the anionic
hydroxypropyl-β-cyclodextrin:poly(decamethylenephosphate) polyrotaxane and evaluation of
1 History of Cyclodextrins
Cramer F, Hettler H (1967) Inclusion compounds of cyclodextrins. Naturwissenschaften
54:625–632
Cramer F, Kampe W (1962) Katalyse der decarboxylierung durch cyclodextrine. Eine modellreaktion fur die wirkungsweise der enzyme. Tetrahedron Lett 8:353–356
Cramer F, Kampe W (1965) Inclusion compounds. 17. Catalysis of decarboxylation by cyclodextrins. A model reaction for mechanism of enzymes. J Am Chem Soc 87:1115–1118
Cramer F, Steinle D (1955) Die wirkungsweise der amylase aus Bacillus macerans. Ann Chem
Justus Liebig 595:81–100
Cramer F, Saenger W, Spatz HC (1967) Inclusion compounds. XIX. The formation of inclusion
compounds of α-cyclodextrin in aqueous solutions. Thermodynamics and kinetics. J Am Chem
Soc 89:14–20
Cramer F, MacKensen G, Sensse K (1969) Über einschlussverbindungen, XX ORD-spektren und
konformation der glucose-einheiten in cyclodextrin. Chem Ber 102:494–508
Crini G (2005) Recent developments in polysaccharide-based materials used as adsorbents in wastewater treatment. Prog Polym Sci 30:38–70. https://doi.org/10.1016/j.progpolymsci.2004.11.002
Crini G (2014) Review: a history of cyclodextrins. Chem Rev 114:10940–10975. https://doi.
org/10.1021/cr500081p
Crini G, Morcellet M (2002) Synthesis and applications of adsorbents containing cyclodextrins.
J Sep Sci 25:789–813. https://doi.org/10.1002/1615-9314(20020901)25:13%3c789:AIDJSSC789%3e3.0.CO;2-J
Crini G, Fourmentin S, Fenyvesi É, Torri G, Fourmentin M, Morin-Crini N (2018) Cyclodextrins,
from molecules to applications. Environ Chem Lett 16:1361–1375. https://doi.org/0.1007/
s10311-018-0763-2
Croft AP, Bartsch RA (1983) Synthesis of chemically modified cyclodextrins. Tetrahedron
9:1417–1474
Cserhati T, Dobrovolszky A, Fenyvesi E, Szejtli J (1983) Beta-cyclodextrin polymer beads as GC
packings. J High Resoult Chromatogr 6:442–443
Cutrone G, Benkovics G, Malanga M, Casas-Solvas JM, Fenyvesi É, Sortino S, García-Fuentes
L, Vargas-Berenguel A (2018) Mannoside and 1,2-mannobioside β-cyclodextrin-scaffolded
NO-photodonors for targeting antibiotic resistant bacteria. Carbohydr Polym 199:649–660.
https://doi.org/10.1016/j.carbpol.2018.07.018
Davis ME, Brewster ME (2004) Cyclodextrin-based pharmaceutics: past, present and future. Natl
Rev 3:1023–1035. https://doi.org/10.1038/nrd1576
Demarco PV, Thakkar AL (1970) Cyclohepta-amylose inclusion complexes. A proton magnetic
resonance study. J Chem Soc Chem Commun 1:2–4. https://doi.org/10.1039/C29700000002
Dietrich HV, Cramer F (1954) Über Einschlussverbindungen, VII. Mitteilung, zür struktur der
jodketten in kanal-einschlussverbindungen. Chem Ber 87:806–817
Dong RJ, Zhou YF, Huang XH, Zhu XY, Lu YF, Shen J (2015) Functional supramolecular polymers
for biomedical applications. Adv Mater 27:498–526. https://doi.org/10.1002/adma.201402975
Duchêne D (1987) Cyclodextrins and their industrial uses. Éditions de Santé, Paris
Duchêne D (1991) New trends in cyclodextrins and derivatives. Éditions de Santé, Paris
Duchêne D, Wouessidjewe D (1990a) The current state of beta-cyclodextrin in pharmaceutics. Int
J Drug Formul Biopharm 36:1–6
Duchêne D, Wouessidjewe D (1990b) Pharmaceutical uses of cyclodextrins and derivatives. Drug
Dev Ind Pharm 16:2487–2499. https://doi.org/10.3109/03639049009058543
Duchêne D, Wouessidjewe D (1992) Industrial uses of cyclodextrins and their derivatives. J Coord
Chem 27:223–236. https://doi.org/10.1080/00958979209407955
Duchêne D, Ponchel G, Wouessidjewe D (1992) Cyclodextrins in targeting – application to nanoparticles. Adv Drug Deliv Rev 36:29–40. https://doi.org/10.1016/S0169-409X(98)00053-2
Duchêne D, Bochot A, Loftsson T (2009) Cyclodextrins and their use in pharmacy and cosmetology. STP Pharm Pratiques 19:15–27
Egele K, Samaddar S, Schneider N, Thompson D, Wenz G (2019) Synthesis of the anionic
hydroxypropyl-β-cyclodextrin:poly(decamethylenephosphate) polyrotaxane and evaluation of
1 History of Cyclodextrins