the foregoing studies [42]. Achieving catalytic supramolecular photochirogenesis
without incorporating sensitizer moiety has been only partially successful [37, 71]
and is still a great challenge to chemists.
18.6 Cross-References
▶ Cyclodextrin-Based Supramolecular Hydrogel
▶ Functionalized Cyclodextrins and Their Applications in Biodelivery
▶ Supramolecular Assembly Constructed from Multi-charged CyclodextrinInduced Aggregation
Acknowledgments We acknowledge the support of this work by the National Natural Science
Foundation of China (No. 21871194, 21572142, 21372165, 21402129 and 21402110), the National
Key Research and Development Program of China (No. 2017YFA0505903), and the Science &
Technology Department of Sichuan Province (2019YJ0160, 2019YJ0090, 2017SZ0021).
References
1. (a) Griesbeck AG, Mattay J (2005) Synthetic organic photochemistry. Marcel Dekker,
New York; (b) Hu R, Zhang C, Pei Z (2013) Mechanistic investigation of light-induced
asymmetric hydrogenation of TMSBO by anoxygenic photosynthetic bacteria. Acta Chim Sin
71(7):1064–1070; (c) Tong L, Lu R, Inoue Y (2006) Asymmetric photochemistry with native
and modified cyclodextrins. Prog Chem 18(5):533–541; (d) Ma L, Chen B, Wu L, Peng L,
Zhang L, Tong Z (2004) Asymmetric photochemical reactions conducted within microreactors.
Prog Chem 16(3):386–392; (e) Yang C, Inoue Y (2014) Supramolecular photochirogenesis.
Chem Soc Rev 43(12):4123–4143
2. Inoue Y, Ramamurthy V (2004) Chiral photochemistry. Marcel Dekker, New York
3. Yang C (2013) Recent progress in supramolecular chiral photochemistry. Chin Chem Lett
24(6):437–441
4. Yang C, Inoue Y (2011) Supramolecular photochirogenesis. In: Ramamurthy V, Inoue Y (eds)
Supramolecular photochemistry: controlling photochemical processes. Wiley, Hoboken, p 115
5. Yang C, Inoue Y Photochirogenesis. In: Griesbeck AG, Oelgemöller M, Ghetti F (eds) CRC
handbook of organic photochemistry and photobiology, vol 1, 3rd edn. Taylaor & Francis
Group, Boca Raton, p 125
6. Brimioulle R, Lenhart D, Maturi MM, Bach T (2015) Enantioselective catalysis of photochemical reactions. Angew Chem Int Ed 54(13):3872–3890
7. Leibovitch M, Olovsson G, Sundarababu G, Ramamurthy V, Scheffer JR, Trotter J (1996)
Asymmetric induction in photochemical reactions conducted in zeolites and in the crystalline
state. J Am Chem Soc 118(5):1219–1220
8. Kuroda Y, Sera T, Ogoshi H (1991) Regioselectivities and stereoselectivities of singlet oxygen
generated by cyclodextrin-sandwiched porphyrin sensitization. Lipoxygenase-like activity.
J Am Chem Soc 113(7):2793–2794
9. Bach T, Bergmann H, Harms K (2000) Enantioselective intramolecular [2+2]photocycloaddition reactions in solution. Angew Chem Int Ed 39(13):2302–2304
10. Bach T, Bergmann H, Grosch B, Harms K (2002) Highly enantioselective intra- and
intermolecular [2 + 2] photocycloaddition reactions of 2-quinolones mediated by a chiral lactam
host: host-guest interactions, product configuration, and the origin of the stereoselectivity in
solution. J Am Chem Soc 124(27):7982–7990
18 Supramolecular Photochirogenesis with Cyclodextrin
531
without incorporating sensitizer moiety has been only partially successful [37, 71]
and is still a great challenge to chemists.
18.6 Cross-References
▶ Cyclodextrin-Based Supramolecular Hydrogel
▶ Functionalized Cyclodextrins and Their Applications in Biodelivery
▶ Supramolecular Assembly Constructed from Multi-charged CyclodextrinInduced Aggregation
Acknowledgments We acknowledge the support of this work by the National Natural Science
Foundation of China (No. 21871194, 21572142, 21372165, 21402129 and 21402110), the National
Key Research and Development Program of China (No. 2017YFA0505903), and the Science &
Technology Department of Sichuan Province (2019YJ0160, 2019YJ0090, 2017SZ0021).
References
1. (a) Griesbeck AG, Mattay J (2005) Synthetic organic photochemistry. Marcel Dekker,
New York; (b) Hu R, Zhang C, Pei Z (2013) Mechanistic investigation of light-induced
asymmetric hydrogenation of TMSBO by anoxygenic photosynthetic bacteria. Acta Chim Sin
71(7):1064–1070; (c) Tong L, Lu R, Inoue Y (2006) Asymmetric photochemistry with native
and modified cyclodextrins. Prog Chem 18(5):533–541; (d) Ma L, Chen B, Wu L, Peng L,
Zhang L, Tong Z (2004) Asymmetric photochemical reactions conducted within microreactors.
Prog Chem 16(3):386–392; (e) Yang C, Inoue Y (2014) Supramolecular photochirogenesis.
Chem Soc Rev 43(12):4123–4143
2. Inoue Y, Ramamurthy V (2004) Chiral photochemistry. Marcel Dekker, New York
3. Yang C (2013) Recent progress in supramolecular chiral photochemistry. Chin Chem Lett
24(6):437–441
4. Yang C, Inoue Y (2011) Supramolecular photochirogenesis. In: Ramamurthy V, Inoue Y (eds)
Supramolecular photochemistry: controlling photochemical processes. Wiley, Hoboken, p 115
5. Yang C, Inoue Y Photochirogenesis. In: Griesbeck AG, Oelgemöller M, Ghetti F (eds) CRC
handbook of organic photochemistry and photobiology, vol 1, 3rd edn. Taylaor & Francis
Group, Boca Raton, p 125
6. Brimioulle R, Lenhart D, Maturi MM, Bach T (2015) Enantioselective catalysis of photochemical reactions. Angew Chem Int Ed 54(13):3872–3890
7. Leibovitch M, Olovsson G, Sundarababu G, Ramamurthy V, Scheffer JR, Trotter J (1996)
Asymmetric induction in photochemical reactions conducted in zeolites and in the crystalline
state. J Am Chem Soc 118(5):1219–1220
8. Kuroda Y, Sera T, Ogoshi H (1991) Regioselectivities and stereoselectivities of singlet oxygen
generated by cyclodextrin-sandwiched porphyrin sensitization. Lipoxygenase-like activity.
J Am Chem Soc 113(7):2793–2794
9. Bach T, Bergmann H, Harms K (2000) Enantioselective intramolecular [2+2]photocycloaddition reactions in solution. Angew Chem Int Ed 39(13):2302–2304
10. Bach T, Bergmann H, Grosch B, Harms K (2002) Highly enantioselective intra- and
intermolecular [2 + 2] photocycloaddition reactions of 2-quinolones mediated by a chiral lactam
host: host-guest interactions, product configuration, and the origin of the stereoselectivity in
solution. J Am Chem Soc 124(27):7982–7990
18 Supramolecular Photochirogenesis with Cyclodextrin
531