메뉴 건너뛰기




Volumn 2, Issue 17, 2000, Pages 2591-2594

1,4-Hydrogen radical transfer as a new and versatile tool for the synthesis of enantiomerically pure 1,2,3-triols

Author keywords

[No Author keywords available]

Indexed keywords


EID: 0000630828     PISSN: 15237060     EISSN: None     Source Type: Journal    
DOI: 10.1021/ol000133p     Document Type: Article
Times cited : (41)

References (53)
  • 3
    • 85065176128 scopus 로고
    • (c) Neale, R. S. Synthesis 1971, 1-15. Hofman-Löffler-Freytag reaction: Wolf, M. E. Chem. Rev. 1963, 63, 55-64. For recent contributions, see:
    • (1971) Synthesis , pp. 1-15
    • Neale, R.S.1
  • 4
    • 0002603882 scopus 로고
    • (c) Neale, R. S. Synthesis 1971, 1-15. Hofman-Löffler-Freytag reaction: Wolf, M. E. Chem. Rev. 1963, 63, 55-64. For recent contributions, see:
    • (1963) Chem. Rev. , vol.63 , pp. 55-64
    • Wolf, M.E.1
  • 32
    • 0026318402 scopus 로고
    • Enders, D.; Gatzweiler, W.; Jegelka, U. Synthesis 1991, 1137-1141. For a review on the use of ketone 1, see: Enders, D.; Bockstiegel, B.; Gatzweiler, W.; Jegelka, U.; Dücker, B. Acros Org. Acta 1998, 4, 5-7.
    • (1991) Synthesis , pp. 1137-1141
    • Enders, D.1    Gatzweiler, W.2    Jegelka, U.3
  • 39
    • 84990135406 scopus 로고
    • For examples of selective axial trapping of closely related radicals, see: (a) Giese, B. Angew. Chem., Int. Ed. Engl. 1989, 28, 8, 969-980.
    • (1989) Angew. Chem., Int. Ed. Engl. , vol.28 , Issue.8 , pp. 969-980
    • Giese, B.1
  • 43
    • 85037496001 scopus 로고    scopus 로고
    • ref 3c
    • (e) ref 3c.
  • 45
    • 85037504506 scopus 로고    scopus 로고
    • note
    • Crystallographic data for 4b have been deposited at the Cambridge Crystallographic Data Centre (File CCDC 145900).
  • 46
    • 85037508848 scopus 로고    scopus 로고
    • note
    • 3 solvent of a NMR tube) and rearranged to acyclic substrate 16. (equation presented)
  • 52
    • 85037503948 scopus 로고    scopus 로고
    • ref 3i
    • (f) ref 3i.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.