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Volumn 62, Issue 5, 1997, Pages 1196-1197

Synthetic studies toward the reveromycins: Asymmetric synthesis of the spiroketal segment of reveromycin B

Author keywords

[No Author keywords available]

Indexed keywords

REVEROMYCIN; REVEROMYCIN B; UNCLASSIFIED DRUG;

EID: 0030889521     PISSN: 00223263     EISSN: None     Source Type: Journal    
DOI: 10.1021/jo962316o     Document Type: Article
Times cited : (36)

References (25)
  • 8
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    • (1980) Tetrahedron Lett. , vol.21 , pp. 1389-1392
    • Ireland, R.E.1    Häbich, D.2
  • 9
    • 0019459346 scopus 로고
    • Ireland, R. E.; Häbich, D. Tetrahedron Lett. 1980, 21, 1389-1392. Ireland, R. E.; Häbich, D. Chem. Ber. 1981, 114, 1418-1427.
    • (1981) Chem. Ber. , vol.114 , pp. 1418-1427
    • Ireland, R.E.1    Häbich, D.2
  • 12
    • 0020530590 scopus 로고
    • Ireland, R. E.; Daub, J. P. J. Org. Chem. 1983, 48, 1303-1312. Ireland, R. E.; Häbich, D.; Norbeck, D. W. J. Am. Chem. Soc. 1985, 107, 3271-3278.
    • (1983) J. Org. Chem. , vol.48 , pp. 1303-1312
    • Ireland, R.E.1    Daub, J.P.2
  • 14
    • 0003586122 scopus 로고
    • Taskinen, E. Ann. Acad. Sci. Fenn. Ser. A 1972, 163, 3. A modified procedure for the synthesis of enol ether 3 can be found in the Supporting Information.
    • (1972) Ann. Acad. Sci. Fenn. Ser. A , vol.163 , pp. 3
    • Taskinen, E.1
  • 17
    • 0000184375 scopus 로고
    • Petasis, N. A.; Bzowej, E. I. J. Am. Chem. Soc. 1990, 112, 6392-6394. Petasis, N. A.; Lu, S.-P. Tetrahedron Lett. 1995, 36, 2393-2396.
    • (1990) J. Am. Chem. Soc. , vol.112 , pp. 6392-6394
    • Petasis, N.A.1    Bzowej, E.I.2
  • 18
    • 0028911641 scopus 로고
    • Petasis, N. A.; Bzowej, E. I. J. Am. Chem. Soc. 1990, 112, 6392-6394. Petasis, N. A.; Lu, S.-P. Tetrahedron Lett. 1995, 36, 2393-2396.
    • (1995) Tetrahedron Lett. , vol.36 , pp. 2393-2396
    • Petasis, N.A.1    Lu, S.-P.2
  • 19
    • 8244258682 scopus 로고    scopus 로고
    • note
    • Less than 5% isomerization was detected after purification by this method.
  • 20
    • 8244262320 scopus 로고    scopus 로고
    • note
    • The stereochemistry at the spirocenter in 12 is controlled in the Diels-Alder reaction by the anomeric effect.
  • 21
    • 30144437908 scopus 로고
    • Murray, R. W.; Jeyaraman, R. J. J. Org. Chem. 1985, 50, 2847-2853. Adam, W.; Bialas J.; Hadjiarapoglou, L. Chem. Ber. 1991, 124, 2377.
    • (1985) J. Org. Chem. , vol.50 , pp. 2847-2853
    • Murray, R.W.1    Jeyaraman, R.J.2


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.