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Volumn , Issue 11, 1996, Pages 1717-1724

Stereoselective synthesis of alcohols, L. Stereoselective synthesis of a C-15/C-27 segment of the venturicidines

Author keywords

Allylboration; Hydroformylation, indirect; Venturicidines

Indexed keywords


EID: 0004373018     PISSN: 09473440     EISSN: None     Source Type: Journal    
DOI: 10.1002/jlac.199619961104     Document Type: Article
Times cited : (12)

References (41)
  • 22
    • 33748895110 scopus 로고
    • (Eds.: G. Helmchen, R. W. Hoffmann, J. Mulzer, E. Schaumann), Thieme, Stuttgart-New York, E 21
    • P. Eilbracht, Hydroformylation in Stereoselective Synthesis (Eds.: G. Helmchen, R. W. Hoffmann, J. Mulzer, E. Schaumann), Thieme, Stuttgart-New York, E 21, 1995, p. 2503-2558.
    • (1995) Hydroformylation in Stereoselective Synthesis , pp. 2503-2558
    • Eilbracht, P.1
  • 26
    • 33748900096 scopus 로고    scopus 로고
    • note
    • 3 contaminant in the reagent led to desilylation. This then gave the chance for the formation of an ipc-alkoxyborane, which underwent intramolecular hydroboration resulting in the wrong regioselectivity.
  • 29
    • 33748889404 scopus 로고    scopus 로고
    • Dissertation, Univ. Marburg
    • R. Göttlich, Dissertation, Univ. Marburg, 1996.
    • (1996)
    • Göttlich, R.1


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.