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Volumn 9, Issue 22, 1998, Pages 3951-3954

A chiron approach to the cyclopropyl lactone oxylipins

Author keywords

[No Author keywords available]

Indexed keywords

CONSTANOLACTONE A; CONSTANOLACTONE B; LACTONE DERIVATIVE; MALIC ACID; UNCLASSIFIED DRUG;

EID: 0032573530     PISSN: 09574166     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0957-4166(98)00413-3     Document Type: Article
Times cited : (20)

References (37)
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    • Nagle, D. G.; Gerwick, W. H. Tetrahedron Lett. 1990, 31, 2995-2998; Nagle, D. G.; Gerwick, W. H. J. Org. Chem. 1994, 59, 7227-7237.
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    • Oxford University Press: Oxford
    • Samuelsson, B. Science 1983, 220, 568-575; Samuelsson, B.; Dahlén, S.-E.; Lindgren, J. A.; Rouzer, C. A.; Serhan, C. N. Science 1987, 237, 1171-1176; Nogrady, T. Medicinal Chemistry, 2nd edn; Oxford University Press: Oxford, 1988; pp. 326-338.
    • (1988) Medicinal Chemistry, 2nd Edn , pp. 326-338
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    • Ph.D. Thesis, University of Reims-Champagne-Ardenne, Reims, February
    • (a) Benkouider, A. Ph.D. Thesis, University of Reims-Champagne-Ardenne, Reims, February 1994.
    • (1994)
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    • Ph.D. Thesis, University L. Pasteur, Strasbourg
    • (b) Barloy-Da Silva, C. Ph.D. Thesis, University L. Pasteur, Strasbourg, 1999.
    • (1999)
    • Barloy-Da Silva, C.1
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    • (b) For another very recent approach toward CL A-B and SL A-B and E-F, see: Varadarajan, S.; Mohapatra, D. K.; Datta, A. Tetrahedron Lett. 1998, 39, 5667-5670 and ibid. 1998, 39, 1075-1078.
    • (1998) Tetrahedron Lett. , vol.39 , pp. 5667-5670
    • Varadarajan, S.1    Mohapatra, D.K.2    Datta, A.3
  • 17
    • 0032568128 scopus 로고    scopus 로고
    • (b) For another very recent approach toward CL A-B and SL A-B and E-F, see: Varadarajan, S.; Mohapatra, D. K.; Datta, A. Tetrahedron Lett. 1998, 39, 5667-5670 and ibid. 1998, 39, 1075-1078.
    • (1998) Tetrahedron Lett. , vol.39 , pp. 1075-1078
  • 26
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    • (b) Direct protection of (S)-1,2,4-butanetriol with para-methoxybenzaldehyde yielded mainly the 6-membered ring ketal, as expected; see: Herradon, B. Tetrahedron: Asymmetry 1991, 2, 191-194; Thiam, M.; Slassi, A.; Chastrette, F.; Amouroux, R. Synth. Commun. 1992, 22, 83-95.
    • (1991) Tetrahedron: Asymmetry , vol.2 , pp. 191-194
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  • 27
    • 0026513181 scopus 로고
    • (b) Direct protection of (S)-1,2,4- butanetriol with para-methoxybenzaldehyde yielded mainly the 6-membered ring ketal, as expected; see: Herradon, B. Tetrahedron: Asymmetry 1991, 2, 191-194; Thiam, M.; Slassi, A.; Chastrette, F.; Amouroux, R. Synth. Commun. 1992, 22, 83-95.
    • (1992) Synth. Commun. , vol.22 , pp. 83-95
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    • The Z isomer was also isolated (1-3%). NMR spectra of the crude mixture showed a selectivity ranging from 96:4 to 85:15 in favor of the E isomer, depending upon the conditions
    • Evans, D. A.; Ng, H. P. Tetrahedron Lett. 1993, 34, 2229-2232. The Z isomer was also isolated (1-3%). NMR spectra of the crude mixture showed a selectivity ranging from 96:4 to 85:15 in favor of the E isomer, depending upon the conditions.
    • (1993) Tetrahedron Lett. , vol.34 , pp. 2229-2232
    • Evans, D.A.1    Ng, H.P.2
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    • note
    • 3).


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.