88
Schlenk H, Sand DM (1961) The association of α- and β-cyclodextrins with organic acids. J Am
Chem Soc 83:2312–2320. https://doi.org/10.1021/ja01471a022
Schlenk H, Sand DM, Tillotson JA (1955) Stabilization of autoxidizable materials by means of
inclusion. J Am Chem Soc 77:3587–3590. https://doi.org/10.1021/ja01618a049
Schlenk H, Gellerman JL, Sand DM (1962) Acylated cyclodextrins as stationary phases for
comparative gas liquid chromatography. Anal Chem 34:1529–1532. https://doi.org/10.1021/
ac60192a006
Schneider HJ (2012) Applications of supramolecular chemistry. CRC Press/Taylor & Francis
Group, Boca Raton
Schneider HJ, Yatsimirsky AK (2000) Principles and methods in supramolecular chemistry. Wiley,
Chichester
Schneiderman E, Stalcup AM (2000) Cyclodextrins: a versatile tool in separation science. J
Chromatogr B 745:83–102. https://doi.org/10.1016/S0378-4347(00)00057-8
Schwimmer S (1953) Evidence for the purity of Schardinger dextrinogenase. Arch Biochem
Biophys 43:108–117. https://doi.org/10.1016/0003-9861(53)90089-7
Scriba GKE (2012) Chiral recognition mechanisms in analytical separation sciences.
Chromatographia 75:815–838. https://doi.org/10.1007/s10337-012-2261-1
Sébille B (1987) Cyclodextrin derivatives. In: Duchêne D (ed) Cyclodextrins and their industrial
uses. Edition de Santé, Paris, pp 351–393
Sharma N, Baldi A (2016) Exploring versatile applications of cyclodextrins: an overview. Drug
Deliv 23:739–757. https://doi.org/10.3109/10717544.2014.938839
Shende P, Trotta F (2019) Diversity of beta-cyclodextrin-based nanosponges for transformation of
actives. Int J Pharm 565:333–350. https://doi.org/10.1016/j.ijpharm.2019.05.015
Sicard PJ, Saniez MH (1987) Chapter 2: Biosynthesis of cycloglycosyltransferase and obtention
of its enzymatic reaction products. In: Duchêne D (ed) Cyclodextrins and their industrial uses.
Éditions de Santé, Paris, pp 77–103
Silva A, Duarte A, Sousa S, Ramos A, Domingues FC (2016) Characterization and antimicrobial
activity of cellulose derivatives films incorporated with a resveratrol inclusion complex. LWT
Food Sci Technol 73:481–489. https://doi.org/10.1016/j.lwt.2016.06.043
Simoes SMN, Veiga F, Torres-Labandeira JJ, Ribeiro ACF, Concheiro A, Alvarez-Lorenzo C
(2014) Syringeable self-assembled cyclodextrin gels for drug delivery. Curr Top Med Chem
14:494–509. https://doi.org/10.2174/1568026613666131219124308
Singh MK, Varun VK, Behera BK (2011) Cosmetotextiles: state of art. Fibres Text East Eur
19:27–33
Sirlin C (1984) Supramolecular catalysis by cyclodextrin and macrocyclic polyether (a review).
Bull Soc Chim France Partie II Chim Moléculaire Organique et Biologique 1-2:5–40
Smolková-Keulemansová E (1982) Cyclodextrins as stationary phases in chromatography. J
Chromatogr 251:17–34
Smolková-Keulemansová E, Krysl S (1980) Inclusion compounds in chromatography. J
Chromatogr 184:347–361. https://doi.org/10.1016/S0021-9673(00)89005-6
Solms J, Egli RH (1965) Harz emit einschlusshohlräumen von cyclodextrin-strukture. Helv Chim
Acta 48:1225–1228
Sonnendecker C, Zimmermann W (2019a) Domain shuffling of cyclodextrin glucanotransferases
for tailored product specificity and thermal stability. FEBS Open Bio 9:384–395. https://doi.
org/10.1002/2211-5463.12588
Sonnendecker C, Zimmermann W (2019b) Change of the product specificity of a cyclodextrin glucanotransferase by semi-rational mutagenesis to synthesize large-ring cyclodextrins. Catalyts
9:242. https://doi.org/10.3390/catal9030242
Sonnendecker C, Melzer S, Zimmermann W (2018) Engineered cyclodextrin glucanotransferases from Bacillus sp. G-825-6 produce large-ring cyclodextrins with high specificity.
MicrobiologyOpen 8(6):e00757. https://doi.org/10.1002/mbo3.757
N. Morin-Crini et al.
Schlenk H, Sand DM (1961) The association of α- and β-cyclodextrins with organic acids. J Am
Chem Soc 83:2312–2320. https://doi.org/10.1021/ja01471a022
Schlenk H, Sand DM, Tillotson JA (1955) Stabilization of autoxidizable materials by means of
inclusion. J Am Chem Soc 77:3587–3590. https://doi.org/10.1021/ja01618a049
Schlenk H, Gellerman JL, Sand DM (1962) Acylated cyclodextrins as stationary phases for
comparative gas liquid chromatography. Anal Chem 34:1529–1532. https://doi.org/10.1021/
ac60192a006
Schneider HJ (2012) Applications of supramolecular chemistry. CRC Press/Taylor & Francis
Group, Boca Raton
Schneider HJ, Yatsimirsky AK (2000) Principles and methods in supramolecular chemistry. Wiley,
Chichester
Schneiderman E, Stalcup AM (2000) Cyclodextrins: a versatile tool in separation science. J
Chromatogr B 745:83–102. https://doi.org/10.1016/S0378-4347(00)00057-8
Schwimmer S (1953) Evidence for the purity of Schardinger dextrinogenase. Arch Biochem
Biophys 43:108–117. https://doi.org/10.1016/0003-9861(53)90089-7
Scriba GKE (2012) Chiral recognition mechanisms in analytical separation sciences.
Chromatographia 75:815–838. https://doi.org/10.1007/s10337-012-2261-1
Sébille B (1987) Cyclodextrin derivatives. In: Duchêne D (ed) Cyclodextrins and their industrial
uses. Edition de Santé, Paris, pp 351–393
Sharma N, Baldi A (2016) Exploring versatile applications of cyclodextrins: an overview. Drug
Deliv 23:739–757. https://doi.org/10.3109/10717544.2014.938839
Shende P, Trotta F (2019) Diversity of beta-cyclodextrin-based nanosponges for transformation of
actives. Int J Pharm 565:333–350. https://doi.org/10.1016/j.ijpharm.2019.05.015
Sicard PJ, Saniez MH (1987) Chapter 2: Biosynthesis of cycloglycosyltransferase and obtention
of its enzymatic reaction products. In: Duchêne D (ed) Cyclodextrins and their industrial uses.
Éditions de Santé, Paris, pp 77–103
Silva A, Duarte A, Sousa S, Ramos A, Domingues FC (2016) Characterization and antimicrobial
activity of cellulose derivatives films incorporated with a resveratrol inclusion complex. LWT
Food Sci Technol 73:481–489. https://doi.org/10.1016/j.lwt.2016.06.043
Simoes SMN, Veiga F, Torres-Labandeira JJ, Ribeiro ACF, Concheiro A, Alvarez-Lorenzo C
(2014) Syringeable self-assembled cyclodextrin gels for drug delivery. Curr Top Med Chem
14:494–509. https://doi.org/10.2174/1568026613666131219124308
Singh MK, Varun VK, Behera BK (2011) Cosmetotextiles: state of art. Fibres Text East Eur
19:27–33
Sirlin C (1984) Supramolecular catalysis by cyclodextrin and macrocyclic polyether (a review).
Bull Soc Chim France Partie II Chim Moléculaire Organique et Biologique 1-2:5–40
Smolková-Keulemansová E (1982) Cyclodextrins as stationary phases in chromatography. J
Chromatogr 251:17–34
Smolková-Keulemansová E, Krysl S (1980) Inclusion compounds in chromatography. J
Chromatogr 184:347–361. https://doi.org/10.1016/S0021-9673(00)89005-6
Solms J, Egli RH (1965) Harz emit einschlusshohlräumen von cyclodextrin-strukture. Helv Chim
Acta 48:1225–1228
Sonnendecker C, Zimmermann W (2019a) Domain shuffling of cyclodextrin glucanotransferases
for tailored product specificity and thermal stability. FEBS Open Bio 9:384–395. https://doi.
org/10.1002/2211-5463.12588
Sonnendecker C, Zimmermann W (2019b) Change of the product specificity of a cyclodextrin glucanotransferase by semi-rational mutagenesis to synthesize large-ring cyclodextrins. Catalyts
9:242. https://doi.org/10.3390/catal9030242
Sonnendecker C, Melzer S, Zimmermann W (2018) Engineered cyclodextrin glucanotransferases from Bacillus sp. G-825-6 produce large-ring cyclodextrins with high specificity.
MicrobiologyOpen 8(6):e00757. https://doi.org/10.1002/mbo3.757
N. Morin-Crini et al.