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Volumn 125, Issue 2, 2003, Pages 350-351

Total synthesis of (+)-13-deoxytedanolide

Author keywords

[No Author keywords available]

Indexed keywords

13 DEOXYTEDANOLIDE; ALKENE; CARBOXYLIC ACID; EPOXIDE; HYDROXYL GROUP; IODIDE; NATURAL PRODUCT; TEDANOLIDE; UNCLASSIFIED DRUG;

EID: 0037438532     PISSN: 00027863     EISSN: None     Source Type: Journal    
DOI: 10.1021/ja0289649     Document Type: Article
Times cited : (94)

References (28)
  • 11
    • 0012473360 scopus 로고    scopus 로고
    • note
    • 1 indicating that the C(17) hydroxyl is positioned to direct the epoxidation.
  • 17
    • 0025058974 scopus 로고
    • Desilylation of (-)-10 and acetonide formation permitted confirmation of the stereochemistry via Rychnovsky-Evans acetonide analysis. See: (a) Rychnovsky, S. D.; Skalitzky, D. J. Tetrahedron Lett. 1990, 31, 945. (b) Rychnovsky, S. D.; Rogers, B.; Yang, G. J. Org. Chem. 1993, 58, 3511. (c) Evans, D. A.; Rieger, D. L.; Gage, J. R. Tetrahedron Lett. 1990, 31, 7099.
    • (1990) Tetrahedron Lett. , vol.31 , pp. 945
    • Rychnovsky, S.D.1    Skalitzky, D.J.2
  • 18
    • 33751385878 scopus 로고
    • Desilylation of (-)-10 and acetonide formation permitted confirmation of the stereochemistry via Rychnovsky-Evans acetonide analysis. See: (a) Rychnovsky, S. D.; Skalitzky, D. J. Tetrahedron Lett. 1990, 31, 945. (b) Rychnovsky, S. D.; Rogers, B.; Yang, G. J. Org. Chem. 1993, 58, 3511. (c) Evans, D. A.; Rieger, D. L.; Gage, J. R. Tetrahedron Lett. 1990, 31, 7099.
    • (1993) J. Org. Chem. , vol.58 , pp. 3511
    • Rychnovsky, S.D.1    Rogers, B.2    Yang, G.3
  • 19
    • 0025608552 scopus 로고
    • Desilylation of (-)-10 and acetonide formation permitted confirmation of the stereochemistry via Rychnovsky-Evans acetonide analysis. See: (a) Rychnovsky, S. D.; Skalitzky, D. J. Tetrahedron Lett. 1990, 31, 945. (b) Rychnovsky, S. D.; Rogers, B.; Yang, G. J. Org. Chem. 1993, 58, 3511. (c) Evans, D. A.; Rieger, D. L.; Gage, J. R. Tetrahedron Lett. 1990, 31, 7099.
    • (1990) Tetrahedron Lett. , vol.31 , pp. 7099
    • Evans, D.A.1    Rieger, D.L.2    Gage, J.R.3
  • 25
    • 0012386243 scopus 로고    scopus 로고
    • note
    • The delicate nature of this intermediate was demonstrated by the requirement to carry the transformation to only partial conversion [i.e., % based on recovered starting material (BORSM)] followed by recyclization.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.