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Volumn , Issue 8, 1997, Pages 1635-1644

A butyrolactone → 1,3-diol strategy for the obtention of Tolypothrix polyethers - Stereoselective synthesis of a key lactone precursor

Author keywords

1,3 Diols; Lactones; Ozonolysis; Reduction, diastereoselective

Indexed keywords


EID: 33748725444     PISSN: 09473440     EISSN: None     Source Type: Journal    
DOI: 10.1002/jlac.199719970804     Document Type: Article
Times cited : (12)

References (65)
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  • 2
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    • Dissertation, Universität Würzburg
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    • (1993)
    • Priepke, H.1
  • 3
    • 0001525650 scopus 로고
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    • (1984) Macrolide Antibiotics , pp. 351-404
    • Omura, S.1    Tanaka, H.2
  • 21
    • 0000020581 scopus 로고
    • Total synthesis of 1c
    • Total syntheses of 1a-d:[6a] Y. Mori, Y. Kohchi, M. Suzuki, J. Org. Chem. 1991, 56, 631-637. - Total synthesis of 1c:
    • (1991) J. Org. Chem. , vol.56 , pp. 631-637
    • Mori, Y.1    Kohchi, Y.2    Suzuki, M.3
  • 22
    • 0000835693 scopus 로고
    • Total syntheses of 1d
    • [6b] Z. Wang, D. Deschênes, J. Am. Chem. Soc. 1992, 114, 1090-1091. - Total syntheses of 1d:
    • (1992) J. Am. Chem. Soc. , vol.114 , pp. 1090-1091
    • Wang, Z.1    Deschênes, D.2
  • 36
    • 33748738565 scopus 로고    scopus 로고
    • Purchased from ALDRICH®.
    • [15a] Purchased from ALDRICH®.
  • 37
    • 33748720666 scopus 로고    scopus 로고
    • [15bl This material must possess ca. 90% ee as revealed by GLC analysis of the compounds 14 (92% ee) and 15 (89% ee) described by H. Priepke and R. Brückner in Liebigs Ann. 1997, 1645-1655; these compounds were prepared from the same batch of 5-16 which we used here.
    • (1997) Liebigs Ann. , pp. 1645-1655
    • Priepke, H.1    Brückner, R.2
  • 39
    • 0342738155 scopus 로고
    • Reviews on oxazoline chemistry: A. I. Meyers, Tetrahedron 1985, 41, 837-860;
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    • Meyers, A.I.1
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* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.