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13. Hu, Y., Liu, C., Wang, J., Ren, X., Kan, X., Dong, Y.: TiO 2 @UiO-68-CIL: A metal–organicframework-based bifunctional composite catalyst for a one-pot sequential asymmetric Morita–
Baylis–Hillman reaction. Inorg. Chem. 58, 4722–4730 (2019)
14. Tanaka, K., Nagase, S., Anami, T., Wierzbick, M., Urbanczyk-Lipkowska, Z.: Enantioselective
Diels-Alder reaction in the confined space of homochiral metal–organic frameworks. RSC Adv.
6, 111436–111439 (2016)
15. Xia, Q., Liu, Y., Li, Z., Gong, W., Cui, Y.: A Cr(salen)-based metal–organic framework as a
versatile catalyst for efficient asymmetric transformations. Chem. Commun. 52, 13167–13170
(2016)
16. Zheng, M., Liu, Y., Wang, C., Liu, S., Lin, W.: Cavity-induced enantioselectivity reversal in a
chiral metal–organic framework Brønsted acid catalyst. Chem. Sci. 3, 2623–2627 (2012)
17. Cui, Y., Ngo, H.L., White, P.S., Lin, W.: Homochiral 3D open frameworks assembled from 1and 2-D coordination polymers. Chem. Comm., 994–995 (2003)
18. Tanaka, K., Sakuragi, K., Ozaki, H., Takada, Y.: Highly enantioselective Friedel-Crafts alkylation of N, N-dialkylanilines with trans-β-nitrostyrene catalyzed by a homochiral metal–organic
framework. Chem. Commun. 54, 6328–6331 (2018)
19. Tanaka, K., Muraoka, T., Hirayama, D., Ohnishi, A.: Highly efficient chromatographic resolution of sulfoxides using a new homochiral MOF–silica composite. Chem. Commun. 48,
8577–8579 (2012)
20. Tanaka, K., Muraoka, T., Otubo, Y., Takahashi, H., Ohnishi, A.: HPLC enantioseparation on
a homochiral MOF–silica composite as a novel chiral stationary phase. RSC Adv. 6, 21293–
21301 (2016)
21. Zhang, M., Pu, Z., Chen, X., Gong, X., Zhu, A., Yuan, L.: Chiral recognition of a 3D chiral
nanoporous metal–organic framework. Chem. Commun. 49, 5201–5203 (2013)
22. Kuang, X., Ma, Y., Su, H., Zhang, J., Dong, Y., Tang, B.: High-performance liquid chromatographic enantioseparation of racemic drugs based on homochiral metal–organic framework.
Anal. Chem. 86, 1277–1281 (2014)
23. Peng, Y., Gong, T., Zhang, K., Lin, X., Liu, Y., Jiang, J., Cui, Y.: Engineering chiral porous
metal–organic frameworks for enantioselective adsorption and separation. Nat. Commun. 5,
4406 (2014)
24. Tanaka, K., Kawakita, T., Morawiak, M., Urbanczyk-Lipkowska, Z.: A novel homochiral
metal–organic framework with an expanded open cage based on (R)-3,3’-bis(6-carboxy2-naphthyl)-2,2’-dihydroxy-1,1’-binaphthyl: synthesis, X-ray structure and efficient HPLC
enantiomer separation. CrystEngComm 21, 487–493 (2019)
K. Tanaka
13. Hu, Y., Liu, C., Wang, J., Ren, X., Kan, X., Dong, Y.: TiO 2 @UiO-68-CIL: A metal–organicframework-based bifunctional composite catalyst for a one-pot sequential asymmetric Morita–
Baylis–Hillman reaction. Inorg. Chem. 58, 4722–4730 (2019)
14. Tanaka, K., Nagase, S., Anami, T., Wierzbick, M., Urbanczyk-Lipkowska, Z.: Enantioselective
Diels-Alder reaction in the confined space of homochiral metal–organic frameworks. RSC Adv.
6, 111436–111439 (2016)
15. Xia, Q., Liu, Y., Li, Z., Gong, W., Cui, Y.: A Cr(salen)-based metal–organic framework as a
versatile catalyst for efficient asymmetric transformations. Chem. Commun. 52, 13167–13170
(2016)
16. Zheng, M., Liu, Y., Wang, C., Liu, S., Lin, W.: Cavity-induced enantioselectivity reversal in a
chiral metal–organic framework Brønsted acid catalyst. Chem. Sci. 3, 2623–2627 (2012)
17. Cui, Y., Ngo, H.L., White, P.S., Lin, W.: Homochiral 3D open frameworks assembled from 1and 2-D coordination polymers. Chem. Comm., 994–995 (2003)
18. Tanaka, K., Sakuragi, K., Ozaki, H., Takada, Y.: Highly enantioselective Friedel-Crafts alkylation of N, N-dialkylanilines with trans-β-nitrostyrene catalyzed by a homochiral metal–organic
framework. Chem. Commun. 54, 6328–6331 (2018)
19. Tanaka, K., Muraoka, T., Hirayama, D., Ohnishi, A.: Highly efficient chromatographic resolution of sulfoxides using a new homochiral MOF–silica composite. Chem. Commun. 48,
8577–8579 (2012)
20. Tanaka, K., Muraoka, T., Otubo, Y., Takahashi, H., Ohnishi, A.: HPLC enantioseparation on
a homochiral MOF–silica composite as a novel chiral stationary phase. RSC Adv. 6, 21293–
21301 (2016)
21. Zhang, M., Pu, Z., Chen, X., Gong, X., Zhu, A., Yuan, L.: Chiral recognition of a 3D chiral
nanoporous metal–organic framework. Chem. Commun. 49, 5201–5203 (2013)
22. Kuang, X., Ma, Y., Su, H., Zhang, J., Dong, Y., Tang, B.: High-performance liquid chromatographic enantioseparation of racemic drugs based on homochiral metal–organic framework.
Anal. Chem. 86, 1277–1281 (2014)
23. Peng, Y., Gong, T., Zhang, K., Lin, X., Liu, Y., Jiang, J., Cui, Y.: Engineering chiral porous
metal–organic frameworks for enantioselective adsorption and separation. Nat. Commun. 5,
4406 (2014)
24. Tanaka, K., Kawakita, T., Morawiak, M., Urbanczyk-Lipkowska, Z.: A novel homochiral
metal–organic framework with an expanded open cage based on (R)-3,3’-bis(6-carboxy2-naphthyl)-2,2’-dihydroxy-1,1’-binaphthyl: synthesis, X-ray structure and efficient HPLC
enantiomer separation. CrystEngComm 21, 487–493 (2019)