메뉴 건너뛰기




Volumn 23, Issue 6-7, 2004, Pages 353-374

Diastereoselective synthesis and antifungal activity of glycosyl isoxazolines

Author keywords

Antifungal activity; Cycloaddition; DBU; Isoxazoline

Indexed keywords

ARTHRODERMA BENHAMIAE; FILOBASIDIELLA NEOFORMANS; FUNGI; SPOROTHRIX SCHENCKII;

EID: 33544461091     PISSN: 07328303     EISSN: 15322327     Source Type: Journal    
DOI: 10.1081/CAR-200037331     Document Type: Article
Times cited : (14)

References (27)
  • 1
    • 11544346529 scopus 로고    scopus 로고
    • Asymmetric 1,3-dipolar cycloaddition reactions
    • Gothelf, K.V.; Jorgensen, K.A. Asymmetric 1,3-dipolar cycloaddition reactions. Chem. Rev. 1998, 98, 863-909.
    • (1998) Chem. Rev. , vol.98 , pp. 863-909
    • Gothelf, K.V.1    Jorgensen, K.A.2
  • 2
    • 33845471903 scopus 로고
    • Stereoselective nitrile oxide cycloaddition to chiral allyl ethers and alcohols: The "Inside alkoxy" effect
    • Houk, K.N.; Moses, S.R.; Wu, Y.D.; Rondan, N.G.; Jager, V.; Schoohe, R.; Fronczec, F.R. Stereoselective nitrile oxide cycloaddition to chiral allyl ethers and alcohols: the "Inside alkoxy" effect. J. Am. Chem. Soc. 1984, 106, 3880-3882.
    • (1984) J. Am. Chem. Soc. , vol.106 , pp. 3880-3882
    • Houk, K.N.1    Moses, S.R.2    Wu, Y.D.3    Rondan, N.G.4    Jager, V.5    Schoohe, R.6    Fronczec, F.R.7
  • 3
    • 0242595732 scopus 로고    scopus 로고
    • Preparation of N-glycosyl hydroxylamines and their oxidation to nitrones for the enantioselective synthesis of isoxazolidines
    • Cicchi, S.; Marradi, M.; Carsi, M.; Faggi, C.; Goti, A. Preparation of N-glycosyl hydroxylamines and their oxidation to nitrones for the enantioselective synthesis of isoxazolidines. Eur. J. Org. Chem. 2003, 4152-4160.
    • (2003) Eur. J. Org. Chem. , pp. 4152-4160
    • Cicchi, S.1    Marradi, M.2    Carsi, M.3    Faggi, C.4    Goti, A.5
  • 6
    • 0034011731 scopus 로고    scopus 로고
    • Linezolid
    • (a) Clemett, D.; Markham, A. Linezolid. Drugs 2000, 59, 815-827;
    • (2000) Drugs , vol.59 , pp. 815-827
    • Clemett, D.1    Markham, A.2
  • 7
    • 18544405939 scopus 로고    scopus 로고
    • Synthesis and evaluation of isourea type glycomimetics related to the indilizidine and trehazolin glycosidase inhibitor families
    • (b) Isabel, M.; Garcia, M.; Perz, P.O.; Mellet, C.O.; Fernandez, G.J.M. Synthesis and evaluation of isourea type glycomimetics related to the indilizidine and trehazolin glycosidase inhibitor families. J. Org. Chem. 2003, 68, 8890-8901.
    • (2003) J. Org. Chem. , vol.68 , pp. 8890-8901
    • Isabel, M.1    Garcia, M.2    Perz, P.O.3    Mellet, C.O.4    Fernandez, G.J.M.5
  • 8
    • 37049104596 scopus 로고
    • An examination of the extent of diastereofacial selection in the reaction of a chiral nitrile oxide with achiral alkenes: A route to β-hydroxy carboxylic acids
    • Kozikowski, A.P.; Kitagawa, Y.; Springer, J.P. An examination of the extent of diastereofacial selection in the reaction of a chiral nitrile oxide with achiral alkenes: a route to β-hydroxy carboxylic acids. J. Chem. Soc. Chem. Comm. 1983, 1460-1462.
    • (1983) J. Chem. Soc. Chem. Comm. , pp. 1460-1462
    • Kozikowski, A.P.1    Kitagawa, Y.2    Springer, J.P.3
  • 9
    • 0001402721 scopus 로고
    • The isoxazoline route to α-methylene lactones
    • Kozikowski, A.P.; Ghos, A.K. The isoxazoline route to α-methylene lactones. Tetrahedron Lett. 1983, 24, 2623-2626.
    • (1983) Tetrahedron Lett. , vol.24 , pp. 2623-2626
    • Kozikowski, A.P.1    Ghos, A.K.2
  • 10
    • 0026495529 scopus 로고
    • A new peptide bond surrogate: 2-isoxazoline in pseudodipeptide chemistry
    • Kim, B.H.; Chung, Y.J.; Keum, G.; Kim, J.; Kim, K. A new peptide bond surrogate: 2-isoxazoline in pseudodipeptide chemistry. Tetrahedron Lett. 1992, 33, 6811-6814.
    • (1992) Tetrahedron Lett. , vol.33 , pp. 6811-6814
    • Kim, B.H.1    Chung, Y.J.2    Keum, G.3    Kim, J.4    Kim, K.5
  • 13
    • 0000949544 scopus 로고
    • Chemistry of naturally occurring polyamines.8. Total synthesis of (+)-Hypusine
    • (a) Tice, C.M.; Ganem, B. Chemistry of naturally occurring polyamines.8. Total synthesis of (+)-Hypusine. J. Org. Chem. 1983, 48, 5048-5050;
    • (1983) J. Org. Chem. , vol.48 , pp. 5048-5050
    • Tice, C.M.1    Ganem, B.2
  • 14
    • 0038277055 scopus 로고    scopus 로고
    • A concise approach to structurally diverse β-amino acids
    • (b) Minter, A.R.; Fullar, A.A.; Mapp, A.K. A concise approach to structurally diverse β-amino acids. J. Am. Chem. Soc. 2003, 125, 6846-6848.
    • (2003) J. Am. Chem. Soc. , vol.125 , pp. 6846-6848
    • Minter, A.R.1    Fullar, A.A.2    Mapp, A.K.3
  • 15
    • 0019807115 scopus 로고
    • Intramolecular nitrile oxide cycloadditon (INOCD) reaction of indole series 2. Total synthesis of racemic and optically active paliclavine and 5-epi-paliclavine
    • (a) Kodkowski, A.P.; Chen, Y.Y. Intramolecular nitrile oxide cycloadditon (INOCD) reaction of indole series 2. Total synthesis of racemic and optically active paliclavine and 5-epi-paliclavine. J. Org. Chem. 1981, 46, 5248-5250;
    • (1981) J. Org. Chem. , vol.46 , pp. 5248-5250
    • Kodkowski, A.P.1    Chen, Y.Y.2
  • 16
    • 33845553544 scopus 로고
    • Reduction of isooxazolines. A case difference
    • (b) Curran, D.P. Reduction of isooxazolines. A case difference. J. Am. Chem. Soc. 1982, 101, 4024-4026;
    • (1982) J. Am. Chem. Soc. , vol.101 , pp. 4024-4026
    • Curran, D.P.1
  • 17
    • 33845550921 scopus 로고
    • Methods of stereoselective cis cyanohydroxylation and carboxyhydroxylation of olefins
    • (c) Kodkowski, A.P.; Adamczyk, M. Methods of stereoselective cis cyanohydroxylation and carboxyhydroxylation of olefins. J. Org. Chem. 1983, 48, 366-372.
    • (1983) J. Org. Chem. , vol.48 , pp. 366-372
    • Kodkowski, A.P.1    Adamczyk, M.2
  • 20
    • 0036430086 scopus 로고    scopus 로고
    • DBU catalysed cyclatic amidation reactions: A convenient synthesis of C-Nucleosides
    • (c) Tewari, N.; Mishra, R.C.; Tiwari, V.K.; Tripathi, R.P. DBU catalysed cyclatic amidation reactions: A convenient synthesis of C-Nucleosides. Synlett 2002, 11, 1779-1782;
    • (2002) Synlett , vol.11 , pp. 1779-1782
    • Tewari, N.1    Mishra, R.C.2    Tiwari, V.K.3    Tripathi, R.P.4
  • 21
    • 0036921557 scopus 로고    scopus 로고
    • Conjugate addition of amines to sugar derived olefinic esters: Synthesis of glycosylated amino esters as DNA Topoisomerase-II Inhibitors
    • (d) Khan, A.R.; Tripathi, R.P.; Tiwari, V.K.; Mishra, R.C.; Reddy, V.J.M.; Saxena, J.K. Conjugate addition of amines to sugar derived olefinic esters: Synthesis of glycosylated amino esters as DNA Topoisomerase-II Inhibitors. J. Carbohydr. Chem. 2002, 21 (6), 591-604;
    • (2002) J. Carbohydr. Chem. , vol.21 , Issue.6 , pp. 591-604
    • Khan, A.R.1    Tripathi, R.P.2    Tiwari, V.K.3    Mishra, R.C.4    Reddy, V.J.M.5    Saxena, J.K.6
  • 22
    • 0037321177 scopus 로고    scopus 로고
    • DBU assisted cyclorelease elimination: Combinatorial synthesis and γ-glutamyl cystein synthetase and glutathione-S-transeferase modulatory activity of C-nucleoside analogs
    • (e) Mishra, R.C.; Tewari, N.; Arora, K.; Ahmad, R.; Tripathi, R.P.; Tiwari, V.K.; Walter, R.D.; Srivatava, A.K. DBU assisted cyclorelease elimination: combinatorial synthesis and γ-glutamyl cystein synthetase and glutathione-S-transeferase modulatory activity of C-nucleoside analogs. Comb. Chem. High Through. Screen. 2003, 6 (14), 37-50.
    • (2003) Comb. Chem. High Through. Screen. , vol.6 , Issue.14 , pp. 37-50
    • Mishra, R.C.1    Tewari, N.2    Arora, K.3    Ahmad, R.4    Tripathi, R.P.5    Tiwari, V.K.6    Walter, R.D.7    Srivatava, A.K.8
  • 23
    • 0014621652 scopus 로고
    • Synthese de C-glycosides derives du pyrazole et de l'isoxazole
    • Tronchet, J.M.J.; Jotter, A.; Hong, N.L. Synthese de C-glycosides derives du pyrazole et de l'isoxazole. Helv. Chim. Acta 1969, 52, 2569-2573.
    • (1969) Helv. Chim. Acta , vol.52 , pp. 2569-2573
    • Tronchet, J.M.J.1    Jotter, A.2    Hong, N.L.3
  • 24
    • 1942467425 scopus 로고    scopus 로고
    • Diastereoselective synthesis of galactopyranosyl amino esters and their transformation into C-nucleosides
    • Katiyar, D.; Mishra, R.C.; Tripathi, R.P. Diastereoselective synthesis of galactopyranosyl amino esters and their transformation into C-nucleosides. J. Carbhydr. Chem. 2004, 23 (1), 49-70.
    • (2004) J. Carbhydr. Chem. , vol.23 , Issue.1 , pp. 49-70
    • Katiyar, D.1    Mishra, R.C.2    Tripathi, R.P.3
  • 25
    • 0001649721 scopus 로고
    • Asymmetric induction in [3 + 2] dipolar cycloaddition reactions of nitrile oxides with chiral (α-oxyallyl) silanes
    • Curran, D.P.; Gothe, S.A. Asymmetric induction in [3 + 2] dipolar cycloaddition reactions of nitrile oxides with chiral (α-oxyallyl) silanes. Tetrahedron Lett. 1988, 44, 3945-3952.
    • (1988) Tetrahedron Lett. , vol.44 , pp. 3945-3952
    • Curran, D.P.1    Gothe, S.A.2
  • 26
    • 0003344514 scopus 로고    scopus 로고
    • Reference method for broth dilution antifungal susceptibility testing of yeasts
    • National Committee for Clinical Laboratory Standards, Wayne, Pa.
    • National Committee for Clinical Laboratory Standards. 1997. Reference method for broth dilution antifungal susceptibility testing of yeasts. Approved Standard M27-A. National Committee for Clinical Laboratory Standards, Wayne, Pa. 17(9), pp. 1-29.
    • (1997) Approved Standard M27-A , vol.17 , Issue.9 , pp. 1-29


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.