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Volumn 4, Issue 10, 1996, Pages 1755-1769

Stereoselective syntheses of substituted pterocarpans with anti-HIV activity, and 5-aza-/5-thia-pterocarpan and 2-aryl-2,3-dihydrobenzofuran analogues

Author keywords

2 Aryl 2,3 dihydrobenzofurans; Azapterocarpans; HIV; Pterocarpans; Thiapterocarpans

Indexed keywords

ANTIVIRUS AGENT; DIHYDROBENZOFURAN DERIVATIVE;

EID: 0030272214     PISSN: 09680896     EISSN: None     Source Type: Journal    
DOI: 10.1016/0968-0896(96)00192-7     Document Type: Article
Times cited : (101)

References (38)
  • 1
    • 0020512371 scopus 로고
    • Herz, W.; Grisebach, H.; Kirby, G. W., Eds.; Springer: Wien
    • 1. For reviews, see (a) Ingham, J.L. In Progress in the Chemistry of Organic Natural Products. Vol. 43; Herz, W.; Grisebach, H.; Kirby, G. W., Eds.; Springer: Wien; 1983; pp 1-266.
    • (1983) Progress in the Chemistry of Organic Natural Products , vol.43 , pp. 1-266
    • Ingham, J.L.1
  • 2
    • 0011884284 scopus 로고
    • Harborne, J. B., Ed.; Chapman & Hall: London; Chapter 5, and previous reviews in this series. See also references cited in refs 2, 4, and 5
    • (b) Dewick, P. M. In The Flavonoids; Harborne, J. B., Ed.; Chapman & Hall: London; 1994; Chapter 5, and previous reviews in this series. See also references cited in refs 2, 4, and 5.
    • (1994) The Flavonoids
    • Dewick, P.M.1
  • 7
    • 0011828437 scopus 로고    scopus 로고
    • For references to reports of antiviral activity of related flavonoids, sec ref 1b
    • (d) For references to reports of antiviral activity of related flavonoids, sec ref 1b.
  • 10
    • 0011887667 scopus 로고    scopus 로고
    • The quinones were prepared by Fremy's salt oxidation of the corresponding 2-alkoxyphenols. Representative experimental details for the preparation of 5e can be found in the Supplementary Material to ref 7a
    • 6. The quinones were prepared by Fremy's salt oxidation of the corresponding 2-alkoxyphenols. Representative experimental details for the preparation of 5e can be found in the Supplementary Material to ref 7a.
  • 16
    • 0011839184 scopus 로고    scopus 로고
    • For other examples of deoxygenations of pterocarpans via this method, see ref 5
    • (b) For other examples of deoxygenations of pterocarpans via this method, see ref 5.
  • 20
    • 0029045726 scopus 로고
    • For another approach to 5-azapterocarpans, see ref 4
    • (b) Engler, T. A.; Chai, W.; Lynch, Jr K. O. Tetrahedron Lett. 1995, 36, 7003. For another approach to 5-azapterocarpans, see ref 4.
    • (1995) Tetrahedron Lett. , vol.36 , pp. 7003
    • Engler, T.A.1    Chai, W.2    Lynch K.O., Jr.3
  • 28
    • 0011900418 scopus 로고    scopus 로고
    • For an example of a Ti(IV)-quinone complex acting as a dehydrogenating agent, see ref 7a
    • (e) For an example of a Ti(IV)-quinone complex acting as a dehydrogenating agent, see ref 7a.
  • 34
    • 0011831751 scopus 로고
    • John Wiley: New York
    • (f) For preparation of 29a, see also Whitmore, F. C.; Hanson, E. R. In Org. Synth., Coll. Vol. I; John Wiley: New York, 1941; p 161.
    • (1941) Org. Synth., Coll. , vol.1 , pp. 161
    • Whitmore, F.C.1    Hanson, E.R.2
  • 36
    • 0011882332 scopus 로고    scopus 로고
    • For descriptions of instrumentation and purifications of solvents/reagents, see refs 5, 7a
    • 16. For descriptions of instrumentation and purifications of solvents/reagents, see refs 5, 7a.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.