메뉴 건너뛰기




Volumn 17, Issue 6, 2012, Pages 7569-7583

Synthesis of main-chain chiral quaternary ammonium polymers for asymmetric catalysis using quaternization polymerization

Author keywords

Chiral polymer; Cinchona alkaloid; Organocatalysis; Quaternary ammonium salt; Quaternization polymerization

Indexed keywords

CINCHONA ALKALOID; CINCHONIDINE; POLYMER; QUATERNARY AMMONIUM DERIVATIVE; THIOL DERIVATIVE;

EID: 84862995003     PISSN: None     EISSN: 14203049     Source Type: Journal    
DOI: 10.3390/molecules17067569     Document Type: Article
Times cited : (17)

References (50)
  • 2
    • 79951680836 scopus 로고    scopus 로고
    • Recent applications of Cinchona alkaloids and their derivatives as catalysts in metal-free asymmetric synthesis
    • Elizabeth, M. O.; Yeboah, S. O.; Girija, S. S. Recent applications of Cinchona alkaloids and their derivatives as catalysts in metal-free asymmetric synthesis. Tetrahedron Lett. 2011, 67, 1725-1762.
    • (2011) Tetrahedron Lett. , vol.67 , pp. 1725-1762
    • Elizabeth, M.O.1    Yeboah, S.O.2    Girija, S.S.3
  • 3
    • 77950521746 scopus 로고    scopus 로고
    • Cinchona alkaloids in asymmetric organocatalysis
    • Marcelli, T.; Hiemstra, H. Cinchona alkaloids in asymmetric organocatalysis. Synthesis 2010, 8, 1229-1279.
    • (2010) Synthesis , vol.8 , pp. 1229-1279
    • Marcelli, T.1    Hiemstra, H.2
  • 4
    • 34447272888 scopus 로고    scopus 로고
    • Recent advances in asymmetric phase-transfer catalysis
    • DOI 10.1002/anie.200601737
    • Ooi, T.; Maruoka, K. Recent advances in asymmetric phase-transfer catalysis. Angew. Chem. Int. Ed. Engl. 2007, 46, 4222-4266. (Pubitemid 47040817)
    • (2007) Angewandte Chemie - International Edition , vol.46 , Issue.23 , pp. 4222-4266
    • Ooi, T.1    Maruoka, K.2
  • 5
    • 33845470711 scopus 로고
    • Efficient catalytic asymmetric alkylations. 1. Enantioselective synthesis of (+)-indacrinone via chiral phase-transfer catalysis
    • Dolling, U.-H.; Davis, P.; Grabowski, E. J. J. Efficient catalytic asymmetric alkylations. 1. Enantioselective synthesis of (+)-indacrinone via chiral phase-transfer catalysis. J. Am. Chem. Soc. 1984, 106, 446-447.
    • (1984) J. Am. Chem. Soc. , vol.106 , pp. 446-447
    • Dolling, U.-H.1    Davis, P.2    Grabowski, E.J.J.3
  • 6
    • 33845185214 scopus 로고
    • The stereoselective synthesis of α-amino acids by phase-transfer catalysis
    • O'Donnell, M. J.; Bennett, W. D.; Wu, S. The stereoselective synthesis of α-amino acids by phase-transfer catalysis. J. Am. Chem. Soc. 1989, 111, 2353-2355.
    • (1989) J. Am. Chem. Soc. , vol.111 , pp. 2353-2355
    • O'Donnell, M.J.1    Bennett, W.D.2    Wu, S.3
  • 7
    • 0033549552 scopus 로고    scopus 로고
    • Re- and si-face-selective nitroaldol reactions catalyzed by a rigid chiral quaternary ammonium salt: A highly stereoselective synthesis of the HIV protease inhibitor amprenavir (Vertex 478)
    • Corey, E. J.; Zhang, F.-Y. re-and si-Face-Selective nitroaldol reactions catalyzed by a rigid chiral quaternary ammonium salt: A highly stereoselective synthesis of the HIV protease inhibitor amprenavir (Vertex 478). Angew. Chem. Int. Ed. Engl. 1999, 38, 1931-1934. (Pubitemid 29339665)
    • (1999) Angewandte Chemie - International Edition , vol.38 , Issue.13-14 , pp. 1931-1934
    • Corey, E.J.1    Zhang, F.-Y.2
  • 8
    • 0033553450 scopus 로고    scopus 로고
    • Enantioselective synthesis of β-hydroxy-α-amino acid esters by aldol coupling using a chiral quaternary ammonium salt as catalyst
    • DOI 10.1016/S0040-4039(99)00636-X, PII S004040399900636X
    • Horikawa, M.; Busch-Peterson, J.; Corey, E. J. Enantioselective synthesis of β-hydroxy-α-amino acid esters by aldol coupling using a chiral quaternary ammonium salt as catalyst. Tetrahedron Lett. 1999, 40, 3843-3846. (Pubitemid 29202245)
    • (1999) Tetrahedron Letters , vol.40 , Issue.20 , pp. 3843-3846
    • Horikawa, M.1    Busch-Petersen, J.2    Corey, E.J.3
  • 9
    • 0027535836 scopus 로고
    • Catalytic asymmetric nitroaldol reaction: An efficient synthesis of (S) propranolol using the lanthanum binaphthol complex
    • Sasai, H.; Itoh, N.; Suzuki, T.; Shibasaki, M. Catalytic asymmetric nitroaldol reaction: An efficient synthesis of (S) propranolol using the lanthanum binaphthol complex. Tetrahedron Lett. 1993, 34, 855-858.
    • (1993) Tetrahedron Lett. , vol.34 , pp. 855-858
    • Sasai, H.1    Itoh, N.2    Suzuki, T.3    Shibasaki, M.4
  • 10
    • 33750533979 scopus 로고    scopus 로고
    • Phase-transfer-catalyzed enantioselective Mannich reaction of malonates with α-amido sulfones
    • DOI 10.1002/adsc.200600250
    • Fini, F.; Bernardi, L.; Herrera, R. P.; Petterson, D.; Ricci, A.; Sgarzani, V. Phase-transfer-catalyzed enantioselective mannich reaction of malonates with á-Amido sulfones. Adv. Synth. Catal. 2006, 348, 2043-2046. (Pubitemid 44662628)
    • (2006) Advanced Synthesis and Catalysis , vol.348 , Issue.15 , pp. 2043-2046
    • Fini, F.1    Bernardi, L.2    Herrera, R.P.3    Pettersen, D.4    Ricci, A.5    Sgarzani, V.6
  • 11
    • 29144448796 scopus 로고    scopus 로고
    • Phase-transfer-catalyzed asymmetric aza-Henry reaction using N-carbamoyl imines generated in situ from α-amido sulfones
    • DOI 10.1002/anie.200502646
    • Fini, F.; Sgarzani, V.; Petterson, D.; Herrera, R. P.; Bernardi, L.; Ricci, A. Phase-transfer-catalyzed asymmetric Aza-henry reaction using N-carbamoyl imines generated in situ from á-Amido sulfones. Angew. Chem. Int. Ed. Engl. 2005, 44, 7975-7978. (Pubitemid 41811723)
    • (2005) Angewandte Chemie - International Edition , vol.44 , Issue.48 , pp. 7975-7978
    • Fini, F.1    Sgarzani, V.2    Pettersen, D.3    Herrera, R.P.4    Bernardi, L.5    Ricci, A.6
  • 12
    • 0002016520 scopus 로고
    • Alkaloid assisted asymmetric synthesis IV additional routes to chiral epoxides
    • Hummelen, J. C.; Wynberg, H. Alkaloid assisted asymmetric synthesis IV additional routes to chiral epoxides. Tetrahedron Lett. 1978, 19, 1089-1092.
    • (1978) Tetrahedron Lett. , vol.19 , pp. 1089-1092
    • Hummelen, J.C.1    Wynberg, H.2
  • 13
    • 33845943259 scopus 로고    scopus 로고
    • Phase transfer catalyzed enantioselective strecker reactions of α-amido sulfones with cyanohydrins
    • DOI 10.1021/jo061566u
    • Herrera, R. P.; Sgarzani, V.; Bernardi, L.; Fini, F.; Petterson, D.; Ricci, A. Phase transfer catalyzed enantioselective strecker reactions of á-Amido sulfones with cyanohydrins. J. Org. Chem. 2006, 71, 9869-9872. (Pubitemid 46032656)
    • (2006) Journal of Organic Chemistry , vol.71 , Issue.26 , pp. 9869-9872
    • Herrera, R.P.1    Sgarzani, V.2    Bernardi, L.3    Fini, F.4    Pettersen, D.5    Ricci, A.6
  • 14
    • 0000359801 scopus 로고
    • New methods and reagents in organic synthesis.75. Asymmetric synthesis of á-hydroxy ketones using chiral phase transfer catalysts
    • Masui, M.; Ando, A.; Shioiri, T. New methods and reagents in organic synthesis.75. Asymmetric synthesis of á-hydroxy ketones using chiral phase transfer catalysts. Tetrahedron Lett. 1988, 29, 2835-2838.
    • (1988) Tetrahedron Lett. , vol.29 , pp. 2835-2838
    • Masui, M.1    Ando, A.2    Shioiri, T.3
  • 15
    • 0034327140 scopus 로고    scopus 로고
    • A fundamentally new approach to enantioselective fluorination based on cinchona alkaloid derivatives/selectfluor combination
    • Shibata, N.; Suzuki, E.; Takeuchi, Y. A fundamentally new approach to enantioselective fluorination based on cinchona alkaloid derivatives/selectfluor combination. J. Am. Chem. Soc. 2000, 122, 10728-10729.
    • (2000) J. Am. Chem. Soc. , vol.122 , pp. 10728-10729
    • Shibata, N.1    Suzuki, E.2    Takeuchi, Y.3
  • 16
    • 0000867232 scopus 로고
    • Chiral Michael addition: Methyl vinyl ketone addition catalyzed by Cinchona alkaloid derivatives
    • Conn, R. S. E.; Lovell, A. V.; Karady, S.; Weinstock, L. M. Chiral Michael addition: Methyl vinyl ketone addition catalyzed by Cinchona alkaloid derivatives. J. Org. Chem. 1986, 51, 4710-4711.
    • (1986) J. Org. Chem. , vol.51 , pp. 4710-4711
    • Conn, R.S.E.1    Lovell, A.V.2    Karady, S.3    Weinstock, L.M.4
  • 17
    • 0032560703 scopus 로고    scopus 로고
    • Highly enantioselective synthesis of cyclic and functionalized α-amino acids by means of a chiral phase transfer catalyst
    • DOI 10.1016/S0040-4039(98)01067-3, PII S0040403998010673
    • Corey, E. J.; Noe, M. C.; Xu, F. Highly enantioselective synthesis of cyclic and functionalized á-amino acids by means of a chiral phase transfer catalyst. Tetrahedron Lett. 1998, 39, 5347-5350. (Pubitemid 28295106)
    • (1998) Tetrahedron Letters , vol.39 , Issue.30 , pp. 5347-5350
    • Corey, E.J.1    Noe, M.C.2    Xu, F.3
  • 18
    • 49349138832 scopus 로고
    • Catalytic asymmetric induction in oxidation reactions. The synthesis of optically active epoxides
    • Helder, R.; Hummelen, J. C.; Lanne, R. W. P. M.; Wiering, J. S.; Wynberg, H. Catalytic asymmetric induction in oxidation reactions. The synthesis of optically active epoxides. Tetrahedron Lett. 1976, 17, 1831-1834.
    • (1976) Tetrahedron Lett. , vol.17 , pp. 1831-1834
    • Helder, R.1    Hummelen, J.C.2    Lanne, R.W.P.M.3    Wiering, J.S.4    Wynberg, H.5
  • 19
    • 0032497664 scopus 로고    scopus 로고
    • Asymmetric epoxidation of α,β-unsaturated ketones under phase-transfer catalyzed conditions
    • PII S0040403998016463
    • Arai, S.; Tsuge, H.; Shioiri, T. Asymmetric epoxidation of á, β-unsaturated ketones under phase-transfer catalyzed conditions. Tetrahedron Lett. 1998, 39, 7563-7566. (Pubitemid 28540856)
    • (1998) Tetrahedron Letters , vol.39 , Issue.41 , pp. 7563-7566
    • Arai, S.1    Tsuge, H.2    Shioiri, T.3
  • 20
    • 0029928540 scopus 로고    scopus 로고
    • A new enantioselective synthesis of N-arylaziridines by phase-transfer catalysis
    • Aires-de-Sousa, J.; Lobo, A. M.; Prabhakar, S. A new enantioselective synthesis of N-arylaziridines by phase-transfer catalysis. Tetrahedron Lett. 1996, 37, 3183-3186.
    • (1996) Tetrahedron Lett. , vol.37 , pp. 3183-3186
    • Aires-De-Sousa, J.1    Lobo, A.M.2    Prabhakar, S.3
  • 21
    • 23744471235 scopus 로고    scopus 로고
    • Synthesis of asymmetric N-arylaziridine derivatives using a new chiral phase-transfer catalyst
    • DOI 10.1055/s-2005-869976, Z00905SS
    • Murugan, E.; Siva, A. Synthesis of asymmetric N-Arylaziridine derivatives using a new chiral phase-transfer catalyst. Synthesis 2005, 2022-2028. (Pubitemid 41138643)
    • (2005) Synthesis , Issue.12 , pp. 2022-2028
    • Murugan, E.1    Siva, A.2
  • 22
    • 85004337882 scopus 로고
    • Asymmetric induction in the borohydride reduction of carbonyl compounds by means of a chiral phase-transfer catalyst
    • Balcells, J.; Colonna, S.; Fornasier, R. Asymmetric induction in the borohydride reduction of carbonyl compounds by means of a chiral phase-transfer catalyst. Synthesis 1976, 1976, 266-267.
    • (1976) Synthesis , vol.1976 , pp. 266-267
    • Balcells, J.1    Colonna, S.2    Fornasier, R.3
  • 23
    • 0030749827 scopus 로고    scopus 로고
    • The asymmetric reduction of ketones using chiral ammonium fluoride salts and silanes
    • DOI 10.1016/S0040-4039(97)01445-7, PII S0040403997014457
    • Drew, M. D.; Lawrence, N. J.; Watson, W.; Bowles, S. A. The asymmetric reduction of ketones using chiral ammonium fluoride salts and silanes. Tetrahedron Lett. 1997, 38, 5857-5860. (Pubitemid 27342065)
    • (1997) Tetrahedron Letters , vol.38 , Issue.33 , pp. 5857-5860
    • Drew, M.D.1    Lawrence, N.J.2    Watson, W.3    Bowles, S.A.4
  • 25
    • 84889816875 scopus 로고    scopus 로고
    • Polymer-supported organocatalysts
    • Synthesis; Puche, J. T., Albericio, F., Eds.; Wiley-VCH: Weinheim, Germany
    • Altava, B.; Burguete, M. I.; Luis, S. V. Polymer-Supported Organocatalysts. In The Power of Functional Resins in Organic, Synthesis; Puche, J. T., Albericio, F., Eds.; Wiley-VCH: Weinheim, Germany, 2008; pp. 247-308.
    • (2008) The Power of Functional Resins in Organic , pp. 247-308
    • Altava, B.1    Burguete, M.I.2    Luis, S.V.3
  • 26
    • 33748257080 scopus 로고    scopus 로고
    • Immobilization of organic catalysts: When, why, and how
    • DOI 10.1002/adsc.200606096
    • Cozzi, F. Immobilization of organic catalysts: When, why, and how. Adv. Synth. Catal. 2006, 348, 1367-1390. (Pubitemid 44318738)
    • (2006) Advanced Synthesis and Catalysis , vol.348 , Issue.12-13 , pp. 1367-1390
    • Cozzi, F.1
  • 27
    • 0141619399 scopus 로고    scopus 로고
    • Polymer-supported organic catalysts
    • Benaglia, M.; Puglisi, A.; Cozzi, F. Polymer-supported organic catalysts. Chem. Rev. 2003, 103, 3401-3430.
    • (2003) Chem. Rev. , vol.103 , pp. 3401-3430
    • Benaglia, M.1    Puglisi, A.2    Cozzi, F.3
  • 28
    • 0032649829 scopus 로고    scopus 로고
    • Asymmetric synthesis of α-amino acids using polymer-supported chiral phase transfer catalysts
    • Zhengpu, Z.; Yongmer, W.; Zhen, W.; Hodge, P. Asymmetric synthesis of α-amino acids using polymer-supported chiral phase transfer catalysts. React. Funct. Polym. 1999, 41, 37-43.
    • (1999) React. Funct. Polym. , vol.41 , pp. 37-43
    • Zhengpu, Z.1    Yongmer, W.2    Zhen, W.3    Hodge, P.4
  • 29
    • 0034714152 scopus 로고    scopus 로고
    • Asymmetric synthesis of α-amino acids using polymer-supported Cinchona alkaloid-derived ammonium salts as chiral phase-transfer catalysts
    • Chinchilla, R.; Mazón, P.; Nájera, C. Asymmetric synthesis of α-amino acids using polymer-supported Cinchona alkaloid-derived ammonium salts as chiral phase-transfer catalysts. Tetrahedron: Asymmetry 2000, 11, 3277-3281.
    • (2000) Tetrahedron: Asymmetry , vol.11 , pp. 3277-3281
    • Chinchilla, R.1    Mazón, P.2    Nájera, C.3
  • 30
    • 0035826551 scopus 로고    scopus 로고
    • New polymer-supported chiral phase-transfer catalysts in the asymmetric synthesis of α-amino acids: The role of a spacer
    • DOI 10.1016/S0957-4166(01)00187-2, PII S0957416601001872
    • Thierry, B.; Plaquevent, J.-C.; Cahard, D. New polymer-supported chiral phase-transfer catalysts in the asymmetric synthesis of α-amino acids: The role of a spacer. Tetrahedron: Asymmertry 2001, 12, 983-986. (Pubitemid 32522716)
    • (2001) Tetrahedron Asymmetry , vol.12 , Issue.7 , pp. 983-986
    • Thierry, B.1    Plaquevent, J.-C.2    Cahard, D.3
  • 31
    • 0034847887 scopus 로고    scopus 로고
    • Solution- and solid-phase approaches in asymmetric phase-transfer catalysis bycinchona alkaloid derivatives
    • Thierry, B.; Perrard, T.; Audourd, C.; Plaquevent, J.-C.; Cahard, D. Solution-and solid-phase approaches in asymmetric phase-transfer catalysis by cinchona alkaloid derivatives. Synthesis 2001, 2001, 1742-1746. (Pubitemid 32831676)
    • (2001) Synthesis , Issue.11 , pp. 1742-1746
    • Thierry, B.1    Perrard, T.2    Audouard, C.3    Plaquevent, J.-C.4    Cahard, D.5
  • 32
    • 0037458537 scopus 로고    scopus 로고
    • Immobilization of catalysts derived from Cinchona alkaloids on modified poly(ethylene glycol)
    • DOI 10.1016/S0957-4166(02)00830-3, PII S0957416602008303
    • Danelli, T.; Annunziata, R.; Benaglia, M.; Cinquini, M.; Cozzi, F.; Tocco, G. Immobilization of catalysts derived from Cinchona alkaloids on modified poly (ethylene glycol). Tetrahedron: Asymmetry 2003, 14, 461-467. (Pubitemid 36173901)
    • (2003) Tetrahedron Asymmetry , vol.14 , Issue.4 , pp. 461-467
    • Danelli, T.1    Annunziata, R.2    Benaglia, M.3    Cinquini, M.4    Cozzi, F.5    Tocco, G.6
  • 33
    • 0038205367 scopus 로고    scopus 로고
    • Poly(ethylene glycol) supported cinchona alkaloids as phase transfer catalysts: Application to the enantioselective synthesis of α-amino acids
    • DOI 10.1016/S0957-4166(03)00279-9
    • Thierry, B.; Plaquevent, J.-C.; Cahard, D. Poly (ethylene glycol) supported cinchona alkaloids as phase transfer catalysts: Application to the enantioselective synthesis of α-amino acids. Tetrahedron: Asymmetry 2003, 14, 1671-1677. (Pubitemid 36694538)
    • (2003) Tetrahedron Asymmetry , vol.14 , Issue.12 , pp. 1671-1677
    • Thierry, B.1    Plaquevent, J.-C.2    Cahard, D.3
  • 34
    • 5444257472 scopus 로고    scopus 로고
    • Polystyrene-anchored Cinchona ammonium salts: Easily recoverable phase-transfer catalysts for the asymmetric synthesis of α-amino acids
    • DOI 10.1002/adsc.200404093
    • Chinchilla, R.; Mazón, P.; Nájera, C. Polystyrene-anchored Cinchona ammonium salts: Easily recoverable phase-transfer catalysts for the asymmetric synthesis of α-amino acids. Adv. Synth. Catal. 2004, 346, 1186-1194. (Pubitemid 39359206)
    • (2004) Advanced Synthesis and Catalysis , vol.346 , Issue.9-10 , pp. 1186-1194
    • Chinchilla, R.1    Mazon, P.2    Najera, C.3
  • 35
    • 33644753817 scopus 로고    scopus 로고
    • Catalytic asymmetric epoxidation of chalcones under poly(ethylene glycol)-supported Cinchona ammonium salt catalyzed conditions
    • DOI 10.1016/j.tetasy.2006.01.029, PII S0957416606000723
    • Lv, J.; Wang, X.; Liu, J.; Zhang, L.; Wang, Y. Catalytic asymmetric epoxidation of chalcones under poly (ethylene glycol)-supported Cinchona ammonium salt catalyzed conditions. Tetrahedron: Asymmetry 2006, 17, 330-335. (Pubitemid 43336155)
    • (2006) Tetrahedron Asymmetry , vol.17 , Issue.3 , pp. 330-335
    • Lv, J.1    Wang, X.2    Liu, J.3    Zhang, L.4    Wang, Y.5
  • 36
    • 33846846194 scopus 로고    scopus 로고
    • Synthesis of new dimeric-PEG-supported cinchona ammonium salts as chiral phase transfer catalysts for the alkylation of Schiff bases with water as the solvent
    • DOI 10.1016/j.tetasy.2006.12.024, PII S0957416607000110
    • Wang, X.; Yin, L.; Wang, Y. Synthesis of new dimeric-PEG-supported cinchona ammonium salts as chiral phase transfer catalysts for the alkylation of Schiff bases with water as the solvent. Tetrahedron Asymmetry 2007, 18, 108-114. (Pubitemid 46205313)
    • (2007) Tetrahedron Asymmetry , vol.18 , Issue.1 , pp. 108-114
    • Wang, X.1    Yin, L.2    Yang, T.3    Wang, Y.4
  • 37
    • 54249141665 scopus 로고    scopus 로고
    • An immobilization method of chiral quaternary ammonium salts onto polymer supports
    • Arakawa, Y.; Haraguchi, N.; Itsuno, S. An Immobilization Method of Chiral Quaternary Ammonium Salts onto Polymer Supports. Angew. Chem. Int. Ed. Engl. 2008, 47, 8232-8235.
    • (2008) Angew. Chem. Int. Ed. Engl. , vol.47 , pp. 8232-8235
    • Arakawa, Y.1    Haraguchi, N.2    Itsuno, S.3
  • 38
    • 43149100814 scopus 로고    scopus 로고
    • Electronically modified polymer-supported cinchona phase-transfer catalysts for asymmetric synthesis of α-alkyl-a-amino acid derivatives
    • Shi, Q.; Lee, Y.-J.; Song, H.; Cheng, M.; Jew, S.-S.; Park, H.-G.; Jeong, B.-S. Electronically modified polymer-supported cinchona phase-transfer catalysts for asymmetric synthesis of α-alkyl-a-amino acid derivatives. Chem. Lett. 2008, 37, 436-437.
    • (2008) Chem. Lett. , vol.37 , pp. 436-437
    • Shi, Q.1    Lee, Y.-J.2    Song, H.3    Cheng, M.4    Jew, S.-S.5    Park, H.-G.6    Jeong, B.-S.7
  • 39
    • 74049157760 scopus 로고    scopus 로고
    • Novel polymer-supported organocatalyst via ion exchange reaction: Facile immobilization of chiral imidazolidin-4-one and its application to Diels-Alder reaction
    • Haraguchi, N.; Takemura, Y.; Itsuno, S. Novel polymer-supported organocatalyst via ion exchange reaction: Facile immobilization of chiral imidazolidin-4-one and its application to Diels-Alder reaction. Tetrahedron Lett. 2010, 51, 1205-1208.
    • (2010) Tetrahedron Lett. , vol.51 , pp. 1205-1208
    • Haraguchi, N.1    Takemura, Y.2    Itsuno, S.3
  • 40
    • 75749096269 scopus 로고    scopus 로고
    • Designing chiral quaternary ammonium polymers: Novel type of polymeric catalyst for asymmetric alkylation reaction
    • Itsuno, S.; Paul, D. K.; Ishimoto, M.; Haraguchi, N. Designing chiral quaternary ammonium polymers: Novel type of polymeric catalyst for asymmetric alkylation reaction. Chem. Lett. 2010, 39, 86-87.
    • (2010) Chem. Lett. , vol.39 , pp. 86-87
    • Itsuno, S.1    Paul, D.K.2    Ishimoto, M.3    Haraguchi, N.4
  • 41
    • 77950425895 scopus 로고    scopus 로고
    • Main-chain ionic polymers: Synthesis of optically active quaternary ammonium sulfonate polymers and their application in asymmetric catalysis
    • Itsuno, S.; Paul, D. K.; Haraguchi, N. Main-chain ionic polymers: Synthesis of optically active quaternary ammonium sulfonate polymers and their application in asymmetric catalysis. J. Am. Chem. Soc. 2010, 132, 2864-2865.
    • (2010) J. Am. Chem. Soc. , vol.132 , pp. 2864-2865
    • Itsuno, S.1    Paul, D.K.2    Haraguchi, N.3
  • 43
    • 84862995515 scopus 로고    scopus 로고
    • Molecular design of chiral quaternary ammonium polymers for asymmetric catalysis applications
    • Parvez, M. M.; Haraguchi, N.; Itsuno, S. Molecular design of chiral quaternary ammonium polymers for asymmetric catalysis applications. Org. Biomol. Chem. 2012, 10, 2870-2877.
    • (2012) Org. Biomol. Chem. , vol.10 , pp. 2870-2877
    • Parvez, M.M.1    Haraguchi, N.2    Itsuno, S.3
  • 44
    • 84863004719 scopus 로고    scopus 로고
    • Synthesis of chiral ionic polymers containing quaternary ammonium sulfonate structure and their catalytic activity in asymmetric alkylation
    • doi:10.1002/jccs.201100724
    • Parvez, M. M.; Salam, M. A.; Haraguchi, N.; Itsuno, S. Synthesis of chiral ionic polymers containing quaternary ammonium sulfonate structure and their catalytic activity in asymmetric alkylation. J. Chin. Chem. Soc. 2012, doi:10.1002/jccs.201100724.
    • (2012) J. Chin. Chem. Soc.
    • Parvez, M.M.1    Salam, M.A.2    Haraguchi, N.3    Itsuno, S.4
  • 45
    • 84859146035 scopus 로고    scopus 로고
    • Design of main-chain polymer of chiral imidazolidinone for asymmetric organocatalysis application
    • Haraguchi, N.; Kiyono, H.; Takemura, Y.; Itsuno, S. Design of main-chain polymer of chiral imidazolidinone for asymmetric organocatalysis application. Chem. Commun. 2012, 48, 4011-4013.
    • (2012) Chem. Commun. , vol.48 , pp. 4011-4013
    • Haraguchi, N.1    Kiyono, H.2    Takemura, Y.3    Itsuno, S.4
  • 46
    • 37049096554 scopus 로고
    • Michael additions catalysed by cinchona alkaloids bound via their vinyl groups to preformed crosslinked polymers
    • Hodge, P.; Khoshdel, E.; Waterhouse, J.; Fréchet, J. M. J. Michael additions catalysed by cinchona alkaloids bound via their vinyl groups to preformed crosslinked polymers. J. Chem. Soc. Perkin Trans. 1 1985, 2327-2331.
    • (1985) J. Chem. Soc. Perkin Trans. , vol.1 , pp. 2327-2331
    • Hodge, P.1    Khoshdel, E.2    Waterhouse, J.3    Fréchet, J.M.J.4
  • 47
    • 0000161052 scopus 로고
    • Probleme und Möglichkeiten der radikalischen Addition von Thiolen an ungesättigte Verbindungen
    • Griesbaum, K. Probleme und Möglichkeiten der radikalischen Addition von Thiolen an ungesättigte Verbindungen. Angew. Chem. 1970, 82, 276-290.
    • (1970) Angew. Chem. , vol.82 , pp. 276-290
    • Griesbaum, K.1
  • 48
    • 84981925786 scopus 로고
    • Problems and possibilities of the free-radical addition of thiols to unsaturated compounds
    • Griesbaum, K. Problems and possibilities of the free-radical addition of thiols to unsaturated compounds. Angew. Chem. Int. Ed. Engl. 1970, 9, 273-287.
    • (1970) Angew. Chem. Int. Ed. Engl. , vol.9 , pp. 273-287
    • Griesbaum, K.1
  • 49
    • 8344226831 scopus 로고    scopus 로고
    • Thiol-enes: Chemistry of the past with promise for the future
    • Hoyle, C. E.; Lee, T. Y.; Roper, T. Thiol-enes: Chemistry of the past with promise for the future. J. Polym. Sci. Part A Polym. Chem. 2004, 42, 5301-5338.
    • (2004) J. Polym. Sci. Part A Polym. Chem. , vol.42 , pp. 5301-5338
    • Hoyle, C.E.1    Lee, T.Y.2    Roper, T.3


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.