23 Asymmetric Catalysis and Chromatographic …
497
Fig. 23.8 (continued)
References
1. Cook, T.R., Zheng, Y., Stang, P.J.: Metal − organic frameworks and self-assembled supramolecular coordination complexes: comparing and contrasting the design, synthesis, and functionality
of metal − organic materials. Chem. Rev. 113, 734–777 (2009)
2. Ma, L., Abney, C., Lin, W.: Enatioselective catalysis with homochiral metal–organic frameworks. Chem. Soc. Rev. 38, 1248–1256 (2009)
3. Peluso, P., Mamane, V., Cossu, S.: Homochiral metal-organic frameworks and their application
in chromatography enantioseparation. J. Chromatogr. A 1363, 11–26 (2014)
4. Tanaka, K., Oda, S., Shiro, M.: A novel chiral porous metal–organic framework: Asymmetric
ring opening reaction of epoxide with amine in the chiral open space. Chem. Commun., 820–822
(2008)
5. Tanaka, K., Kinoshita, M., Kayahara, J., Uebayashi, Y., Nakaji, K., Morrawiak, M., UrbanczykLipkowska, Z.: Asymmetric ring-opening reaction of meso-epoxides with aromatic amines
using homochiral metal–organic frameworks as recyclable heterogeneous catalysts. RSC Adv.
8, 28146–28159 (2018)
6. Doitomi, K., Xu, K., Hirao, H.: The mechanism of an asymmetric ring-opening reaction of
epoxide with amine catalyzed by a metal–organic framework: insights from combined quantum
mechanics and molecular mechanics calculations. Dalton Trans. 46, 3470–3481 (2017)
7. Regati, S., He, Y., Thimmaiah, M., Li, P., Xiang, S., Chen, B., Cong-Gui Zhao, J.: Enantioselective ring-opening of meso-epoxides by aromatic amines catalyzed by a homochiral
metal–organic framework. Chem. Commun., 49, 9836–9838 (2013)
8. Tanaka, K., Kubo, K., Iida, K., Otani, K., Murase, T., Yanamoto, D., Shiro, M.: Asymmetric
catalytic sulfoxidation with H 2 O 2 using chiral copper metal–organic framework crystals. Asian
J. Org. Chem. 2, 1055–1060 (2013)
9. Falkowski, J.M., Sawano, T., Zhang, T., Tsun, G., Chen, Y., Lockard, J.V., Lin, W.: Privileged phosphine-based metal–organic frameworks for broad-scope asymmetric catalysis. J.
Am. Chem. Soc. 136, 5213–5216 (2014)
10. Sawano, T., Ji, P., McIsaac, A.R., Lin, Z., Abney, C.W., Lin, W.: The first chiral dienebased metal–organic frameworks for highly enantioselective carbon–carbon bond formation
reactions. Chem. Sci. 6, 7163–7168 (2015)
11. Xi, W., Liu, Y., Xia, Q., Li, Z., Cui, Y.: Direct and post-synthesis incorporation of chiral
metallosalen catalysts into metal–organic frameworks for asymmetric organic transformations.
Chem. Eur. J. 21, 12581–12585 (2015)
12. Fan, Y., Ren, Y., Li, J., Yue, C., Jiang, H.: Enhanced activity and enantioselectivity of Henry
reaction by the postsynthetic reduction modification for a chiral Cu(salen)-based metal–organic
framework. Inorg. Chem. 57, 11986–11994 (2018)
497
Fig. 23.8 (continued)
References
1. Cook, T.R., Zheng, Y., Stang, P.J.: Metal − organic frameworks and self-assembled supramolecular coordination complexes: comparing and contrasting the design, synthesis, and functionality
of metal − organic materials. Chem. Rev. 113, 734–777 (2009)
2. Ma, L., Abney, C., Lin, W.: Enatioselective catalysis with homochiral metal–organic frameworks. Chem. Soc. Rev. 38, 1248–1256 (2009)
3. Peluso, P., Mamane, V., Cossu, S.: Homochiral metal-organic frameworks and their application
in chromatography enantioseparation. J. Chromatogr. A 1363, 11–26 (2014)
4. Tanaka, K., Oda, S., Shiro, M.: A novel chiral porous metal–organic framework: Asymmetric
ring opening reaction of epoxide with amine in the chiral open space. Chem. Commun., 820–822
(2008)
5. Tanaka, K., Kinoshita, M., Kayahara, J., Uebayashi, Y., Nakaji, K., Morrawiak, M., UrbanczykLipkowska, Z.: Asymmetric ring-opening reaction of meso-epoxides with aromatic amines
using homochiral metal–organic frameworks as recyclable heterogeneous catalysts. RSC Adv.
8, 28146–28159 (2018)
6. Doitomi, K., Xu, K., Hirao, H.: The mechanism of an asymmetric ring-opening reaction of
epoxide with amine catalyzed by a metal–organic framework: insights from combined quantum
mechanics and molecular mechanics calculations. Dalton Trans. 46, 3470–3481 (2017)
7. Regati, S., He, Y., Thimmaiah, M., Li, P., Xiang, S., Chen, B., Cong-Gui Zhao, J.: Enantioselective ring-opening of meso-epoxides by aromatic amines catalyzed by a homochiral
metal–organic framework. Chem. Commun., 49, 9836–9838 (2013)
8. Tanaka, K., Kubo, K., Iida, K., Otani, K., Murase, T., Yanamoto, D., Shiro, M.: Asymmetric
catalytic sulfoxidation with H 2 O 2 using chiral copper metal–organic framework crystals. Asian
J. Org. Chem. 2, 1055–1060 (2013)
9. Falkowski, J.M., Sawano, T., Zhang, T., Tsun, G., Chen, Y., Lockard, J.V., Lin, W.: Privileged phosphine-based metal–organic frameworks for broad-scope asymmetric catalysis. J.
Am. Chem. Soc. 136, 5213–5216 (2014)
10. Sawano, T., Ji, P., McIsaac, A.R., Lin, Z., Abney, C.W., Lin, W.: The first chiral dienebased metal–organic frameworks for highly enantioselective carbon–carbon bond formation
reactions. Chem. Sci. 6, 7163–7168 (2015)
11. Xi, W., Liu, Y., Xia, Q., Li, Z., Cui, Y.: Direct and post-synthesis incorporation of chiral
metallosalen catalysts into metal–organic frameworks for asymmetric organic transformations.
Chem. Eur. J. 21, 12581–12585 (2015)
12. Fan, Y., Ren, Y., Li, J., Yue, C., Jiang, H.: Enhanced activity and enantioselectivity of Henry
reaction by the postsynthetic reduction modification for a chiral Cu(salen)-based metal–organic
framework. Inorg. Chem. 57, 11986–11994 (2018)