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Volumn 11, Issue 5-6, 1999, Pages 483-486

Synthesis of 2-aryloxy acids analogues of clofibrate via dynamic kinetic resolution

Author keywords

(4S) 4 isopropyl 1,3 oxazolidin 2 one; 2 aryloxy acids; Clofibrate analogues; Dynamic kinetic resolution; Imide derivatives

Indexed keywords

4 ISOPROPYL 1,3 OXAZOLIDIN 2 ONE; CLOFIBRATE DERIVATIVE; UNCLASSIFIED DRUG;

EID: 0032997638     PISSN: 08990042     EISSN: None     Source Type: Journal    
DOI: 10.1002/(SICI)1520-636X(1999)11:5/6<483::AID-CHIR21>3.0.CO;2-I     Document Type: Conference Paper
Times cited : (12)

References (13)
  • 2
    • 0029981637 scopus 로고    scopus 로고
    • Differential eudismic ratios in the antagonism of human platelet function by phenoxy-and thiophenoxyacetic acids
    • Romstedt KJ, Lei L, Feller DR, Witiak DT, Loiodice F, Tortorella V. Differential eudismic ratios in the antagonism of human platelet function by phenoxy-and thiophenoxyacetic acids. Farmaco 1996;51:107-114.
    • (1996) Farmaco , vol.51 , pp. 107-114
    • Romstedt, K.J.1    Lei, L.2    Feller, D.R.3    Witiak, D.T.4    Loiodice, F.5    Tortorella, V.6
  • 4
    • 0030890262 scopus 로고    scopus 로고
    • Stereoselective effects of chiral clofibric acid analogs on rat peroxisome proliferator-activated receptor α (rPPARα) activation and peroxisomal fatty acid β-oxidation
    • Rangwala SM, O'Brien ML, Tortorella V, Longo A, Loiodice F, Noonan DJ, Feller DR. Stereoselective effects of chiral clofibric acid analogs on rat peroxisome proliferator-activated receptor α (rPPARα) activation and peroxisomal fatty acid β-oxidation. Chirality 1997;9:93-97.
    • (1997) Chirality , vol.9 , pp. 93-97
    • Rangwala, S.M.1    O'Brien, M.L.2    Tortorella, V.3    Longo, A.4    Loiodice, F.5    Noonan, D.J.6    Feller, D.R.7
  • 5
    • 0345389970 scopus 로고    scopus 로고
    • Direct resolution of α-monoalkyl-α-aryloxyacetic acids via ester or imide derivatives
    • Amoroso R, Bettoni G, Tricca ML, Loiodice F, Ferorelli S. Direct resolution of α-monoalkyl-α-aryloxyacetic acids via ester or imide derivatives. Farmaco 1998a;53:73-79.
    • (1998) Farmaco , vol.53 , pp. 73-79
    • Amoroso, R.1    Bettoni, G.2    Tricca, M.L.3    Loiodice, F.4    Ferorelli, S.5
  • 6
    • 0002893037 scopus 로고    scopus 로고
    • N2 reaction from diastereomerically enriched α-bromo esters
    • N2 reaction from diastereomerically enriched α-bromo esters. Synlett 1998b:363-364.
    • (1998) Synlett , pp. 363-364
    • Amoroso, R.1    Bettoni, G.2    Tricca, M.L.3
  • 7
    • 0026751962 scopus 로고
    • A new process for the enantioselective synthesis of chiral α-aryloxy- and α-hydroxy acids
    • Corey EJ, Link JO. A new process for the enantioselective synthesis of chiral α-aryloxy- and α-hydroxy acids. Tetrahedron Lett 1992;33:3431-3434.
    • (1992) Tetrahedron Lett , vol.33 , pp. 3431-3434
    • Corey, E.J.1    Link, J.O.2
  • 8
    • 0028819296 scopus 로고
    • Diasteroselective synthesis of α-bromo amides leading to diastereometrically enriched α-amino-, α-hydroxy- and α-thiocarboxylic acid derivatives
    • Ward RS, Pelter A, Goubet D, Pritchard MC. Diasteroselective synthesis of α-bromo amides leading to diastereometrically enriched α-amino-, α-hydroxy- and α-thiocarboxylic acid derivatives. Tetrahedron: Asymmetry 1995a;6:496-498.
    • (1995) Tetrahedron: Asymmetry , vol.6 , pp. 496-498
    • Ward, R.S.1    Pelter, A.2    Goubet, D.3    Pritchard, M.C.4
  • 9
    • 0028065056 scopus 로고
    • N2 reaction of the (R)-pantolactone ester of racemic α-halo carboxylic acids with aryloxides. A synthesis of (S)-2-aryloxy and (S)-2-hydroxy acids
    • N2 reaction of the (R)-pantolactone ester of racemic α-halo carboxylic acids with aryloxides. A synthesis of (S)-2-aryloxy and (S)-2-hydroxy acids. J Org Chem 1994;59:4683-4686.
    • (1994) J Org Chem , vol.59 , pp. 4683-4686
    • Koh, K.1    Durst, T.2
  • 10
    • 0029928212 scopus 로고    scopus 로고
    • Stereoselective synthesis of 2-aryloxy acids from lactamide derived esters of racemic α-halo carboxylic acids
    • Devine PN, Dolling UH, Held RM, Jr, Tschaen DM. Stereoselective synthesis of 2-aryloxy acids from lactamide derived esters of racemic α-halo carboxylic acids. Tetrahedron Lett 1996;37:2683-2686.
    • (1996) Tetrahedron Lett , vol.37 , pp. 2683-2686
    • Devine, P.N.1    Dolling, U.H.2    Held, R.M.3    Tschaen, D.M.4
  • 11
    • 0029103383 scopus 로고
    • Dynamic kinetic resolution
    • Ward RS. Dynamic kinetic resolution. Tetrahedron: Asymmetry. 1995b;6:1475-1490.
    • (1995) Tetrahedron: Asymmetry , vol.6 , pp. 1475-1490
    • Ward, R.S.1
  • 12
    • 0001597804 scopus 로고
    • Contrasteric carboximide hydrolysis with lithim hydroperoxide
    • Evans DA, Britton TC, Ellman JA. Contrasteric carboximide hydrolysis with lithim hydroperoxide. Tetrahedron Lett 1987;28:6141-6143.
    • (1987) Tetrahedron Lett , vol.28 , pp. 6141-6143
    • Evans, D.A.1    Britton, T.C.2    Ellman, J.A.3
  • 13
    • 0026710206 scopus 로고
    • Chiral α-substituted α-aryloxyacetic acids: Synthesis, absolute configuration, chemical resolution and direct separation by HPLC
    • Bettoni G, Ferorelli S, Loiodice F, Tangari N, Tortorella V, Gasparrini F, Misiti D, Villani C. Chiral α-substituted α-aryloxyacetic acids: Synthesis, absolute configuration, chemical resolution and direct separation by HPLC. Chirality 1992;4:193-203.
    • (1992) Chirality , vol.4 , pp. 193-203
    • Bettoni, G.1    Ferorelli, S.2    Loiodice, F.3    Tangari, N.4    Tortorella, V.5    Gasparrini, F.6    Misiti, D.7    Villani, C.8


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.