메뉴 건너뛰기




Volumn 34, Issue 4, 2004, Pages 727-734

Zirconium (IV) Chloride Catalyzed Ring Opening of Epoxides with Aromatic Amines

Author keywords

Aromatic amine; Epoxide; Zirconium (IV) chloride

Indexed keywords

ACETONITRILE; AMINOALCOHOL; ANILINE; AROMATIC AMINE; BETA AMINOALCOHOL; EPOXIDE; UNCLASSIFIED DRUG; ZIRCONIUM CHLORIDE; ZIRCONIUM DERIVATIVE;

EID: 1542426097     PISSN: 00397911     EISSN: None     Source Type: Journal    
DOI: 10.1081/SCC-120027721     Document Type: Article
Times cited : (31)

References (23)
  • 1
    • 0033549552 scopus 로고    scopus 로고
    • re- and si-Face-selective nitroaldol reactions catalyzed by a rigid chiral quartemary ammonium salt: A highly stereoselective synthesis of the HIV protease inhibitor amprenavir (vertex 478)
    • (a) Corey, E.J.; Zhang, F. re- and si-Face-selective nitroaldol reactions catalyzed by a rigid chiral quartemary ammonium salt: a highly stereoselective synthesis of the HIV protease inhibitor amprenavir (vertex 478). Angew. Chem. Int. Ed. 1999, 38, 1931;
    • (1999) Angew. Chem. Int. Ed. , vol.38 , pp. 1931
    • Corey, E.J.1    Zhang, F.2
  • 2
    • 0024328329 scopus 로고
    • Synthesis, in vitro acetylcholine-storage-blocking activities, and biological properties of derivatives and anlogues of trans-2-(4-phenyl piperidino) cyclohexanol (vesamicol)
    • (b) Rogers, G.A.; Parson, S.M.; Anderson, D.C.; Nilsson, L.M.; Bahr, B.A.; Komreich, W.D.; Kaufman, R.; Jacobson, R.S.; Kirtman, B. Synthesis, in vitro acetylcholine-storage-blocking activities, and biological properties of derivatives and anlogues of trans-2-(4-phenyl piperidino) cyclohexanol (vesamicol). J. Med. Chem. 1989, 32, 1217;
    • (1989) J. Med. Chem. , vol.32 , pp. 1217
    • Rogers, G.A.1    Parson, S.M.2    Anderson, D.C.3    Nilsson, L.M.4    Bahr, B.A.5    Komreich, W.D.6    Kaufman, R.7    Jacobson, R.S.8    Kirtman, B.9
  • 3
    • 0030927125 scopus 로고    scopus 로고
    • Solution-phase synthesis of a β-amino alcohol combinatorial library
    • (c) Chng, B.L.; Ganesan, A. Solution-phase synthesis of a β-amino alcohol combinatorial library. Bioorg. Med. Chem. Lett. 1997, 7, 1511.
    • (1997) Bioorg. Med. Chem. Lett. , vol.7 , pp. 1511
    • Chng, B.L.1    Ganesan, A.2
  • 4
    • 33947292866 scopus 로고
    • Oxidation by metal salts VII syntheses based on the selective oxidation of free radicals, oxidation by metal salts VII the decomposition of ceric carboxylates in the presence of olefins and aromatic hydrocarbons
    • (a) Heiba, E.I.; Dessau, R.M. Oxidation by metal salts VII syntheses based on the selective oxidation of free radicals, oxidation by metal salts VII the decomposition of ceric carboxylates in the presence of olefins and aromatic hydrocarbons. J. Am. Chem. Soc. 1971, 93, 524, 995;
    • (1971) J. Am. Chem. Soc. , vol.93 , pp. 524
    • Heiba, E.I.1    Dessau, R.M.2
  • 5
    • 33947091649 scopus 로고
    • Oxidation by metal salts IX formation of cyclic ketones
    • (b) Oxidation by metal salts IX formation of cyclic ketones. Ibid. 1972, 94, 2888;
    • (1972) J. Am. Chem. Soc. , vol.94 , pp. 2888
  • 6
    • 0000096998 scopus 로고
    • Aromatic acetylation promoted by manganese (III) and cerium (IV) salts
    • (c) Kurt, M.E.; Baru, V.; Ngugen, P.N. Aromatic acetylation promoted by manganese (III) and cerium (IV) salts. J. Org. Chem. 1984, 49, 1603;
    • (1984) J. Org. Chem. , vol.49 , pp. 1603
    • Kurt, M.E.1    Baru, V.2    Ngugen, P.N.3
  • 7
    • 0000599867 scopus 로고
    • Dimethyl arylmalonates from cerium (IV) ammonium nitrate promoted reactions of dimethyl malonate with aromatic compounds in methanol
    • (d) Baciocchi, E.; Aira, D.D.; Ruzziconi, R. Dimethyl arylmalonates from cerium (IV) ammonium nitrate promoted reactions of dimethyl malonate with aromatic compounds in methanol. Tetrahedron Lett. 1986, 27, 2763;
    • (1986) Tetrahedron Lett. , vol.27 , pp. 2763
    • Baciocchi, E.1    Aira, D.D.2    Ruzziconi, R.3
  • 8
    • 0000802984 scopus 로고
    • 1,2- and 1,4-addition in the reactions of carbonyl compounds with 1,3-butadien induced by cerium (IV) ammonium nitrate
    • (e) Baciocchi, E.; Ruzziconi, R. 1,2- and 1,4-addition in the reactions of carbonyl compounds with 1,3-butadien induced by cerium (IV) ammonium nitrate. J. Org. Chem. 1986, 51, 1645.
    • (1986) J. Org. Chem. , vol.51 , pp. 1645
    • Baciocchi, E.1    Ruzziconi, R.2
  • 11
    • 0022455206 scopus 로고
    • Synthesis and α-D-glucosidase inhibitory activity of n-substituted valiolamine derivatives as potential oral antidiabetic agents
    • Horii, S.; Fukase, H.; Matsuo, T.; Kameda, Y.; Asano, N.; Matsui, K. Synthesis and α-D-glucosidase inhibitory activity of n-substituted valiolamine derivatives as potential oral antidiabetic agents. J. Med. Chem. 1986, 29, 1038.
    • (1986) J. Med. Chem. , vol.29 , pp. 1038
    • Horii, S.1    Fukase, H.2    Matsuo, T.3    Kameda, Y.4    Asano, N.5    Matsui, K.6
  • 12
    • 33947299941 scopus 로고
    • 1,2,3-Oxathiazolidines-a new heterocyclic system
    • (a) Deyrup, J.A.; Moyer, C.L. 1,2,3-Oxathiazolidines-a new heterocyclic system. J. Org. Chem. 1969, 34, 175;
    • (1969) J. Org. Chem. , vol.34 , pp. 175
    • Deyrup, J.A.1    Moyer, C.L.2
  • 13
    • 0015753431 scopus 로고
    • Synthesis of β-amino alcohols via spiro-oxirane intermediates
    • (b) Crooks, P.A.; Szyndler, R. Synthesis of β-amino alcohols via spiro-oxirane intermediates. Chem. Ind. (London) 1973, 1111.
    • (1973) Chem. Ind. (London) , pp. 1111
    • Crooks, P.A.1    Szyndler, R.2
  • 14
    • 0030597092 scopus 로고    scopus 로고
    • Lithium trifluromethanesulfonate catalyzed aminolysis of oxiranes
    • LiOTf
    • (a) Auge, J.; Leroy, F. Lithium trifluromethanesulfonate catalyzed aminolysis of oxiranes. Tetrahedron Lett. 1996, 37, 7715 (LiOTf);
    • (1996) Tetrahedron Lett. , vol.37 , pp. 7715
    • Auge, J.1    Leroy, F.2
  • 19
    • 0033534609 scopus 로고    scopus 로고
    • An efficient method for cleavage of epoxides with aromatic amines
    • Sekar, G.; Singh, V.K. An efficient method for cleavage of epoxides with aromatic amines. J. Org. Chem. 1999, 64, 287.
    • (1999) J. Org. Chem. , vol.64 , pp. 287
    • Sekar, G.1    Singh, V.K.2
  • 20
    • 0033054019 scopus 로고    scopus 로고
    • 4) catalyzed highly chemoselective and efficient transthioacetalization of acetals
    • 4) catalyzed highly chemoselective and efficient transthioacetalization of acetals. Synlett 1999, 3, 319;
    • (1999) Synlett , vol.3 , pp. 319
    • Firouzabadi, H.1    Iranpoor, N.2    Karimi, B.3
  • 21
    • 0030600192 scopus 로고    scopus 로고
    • Zirconium (IV) chloride silica catalyzed thioacetalization of carbonyl compounds
    • (b) Patney, H.K.; Margan, S. Zirconium (IV) chloride silica catalyzed thioacetalization of carbonyl compounds. Tetrahedron Lett. 1996, 37, 4621.
    • (1996) Tetrahedron Lett. , vol.37 , pp. 4621
    • Patney, H.K.1    Margan, S.2
  • 22
    • 0033020490 scopus 로고    scopus 로고
    • Zirconium (IV) tetrachloride catalyzed highly chemoselective and efficient acetalization of carbonyl compounds
    • Firouzabadi, H.; Iranpoor, N.; Karimi, B. Zirconium (IV) tetrachloride catalyzed highly chemoselective and efficient acetalization of carbonyl compounds. Synlett 1999, 3, 321.
    • (1999) Synlett , vol.3 , pp. 321
    • Firouzabadi, H.1    Iranpoor, N.2    Karimi, B.3
  • 23
    • 0037009712 scopus 로고    scopus 로고
    • A practical synthesis of chloromethylester from acid chlorides and trioxanes or paraformaldehyde promoted by zirconium tetrachloride
    • Udry, K.B.; Rajaraman, S.; Soundararajan, N. A practical synthesis of chloromethylester from acid chlorides and trioxanes or paraformaldehyde promoted by zirconium tetrachloride. Tetrahedron Lett. 2002, 43, 6317.
    • (2002) Tetrahedron Lett. , vol.43 , pp. 6317
    • Udry, K.B.1    Rajaraman, S.2    Soundararajan, N.3


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.