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Volumn 39, Issue 13, 2000, Pages 2294-2297

Highly diastereoselective synthesis of monocyclic and bicyclic secondary diorganozinc reagents with defined configuration

Author keywords

C C coupling; Configuration stability; Diastereoselective synthesis; Transmetalations

Indexed keywords

ZINC DERIVATIVE;

EID: 0034600780     PISSN: 14337851     EISSN: None     Source Type: Journal    
DOI: None     Document Type: Article
Times cited : (46)

References (34)
  • 7
    • 0000854142 scopus 로고    scopus 로고
    • D. Hoppe, T. Hense, Angew. Chem. 1997, 109, 2376-2410; Angew. Chem. Int. Ed. Engl. 1997, 36, 2282-2316.
    • (1997) Angew. Chem. , vol.109 , pp. 2376-2410
    • Hoppe, D.1    Hense, T.2
  • 8
    • 0030694010 scopus 로고    scopus 로고
    • D. Hoppe, T. Hense, Angew. Chem. 1997, 109, 2376-2410; Angew. Chem. Int. Ed. Engl. 1997, 36, 2282-2316.
    • (1997) Angew. Chem. Int. Ed. Engl. , vol.36 , pp. 2282-2316
  • 12
    • 0032476136 scopus 로고    scopus 로고
    • c) D. J. Pippel, G. A. Weisenburger, S. R. Wilson, P. Beak, Angew. Chem. 1998, 110, 2600-2602; Angew. Chem. Int. Ed. 1998, 37, 2522-2524.
    • (1998) Angew. Chem. Int. Ed. , vol.37 , pp. 2522-2524
  • 14
    • 0030935084 scopus 로고    scopus 로고
    • L. Micouin, M. Oestreich, P. Knochel, Angew. Chem. 1997, 109, 274- 276; Angew. Chem. Int. Ed. Engl. 1997, 36, 245-246.
    • (1997) Angew. Chem. Int. Ed. Engl. , vol.36 , pp. 245-246
  • 26
    • 85007625376 scopus 로고    scopus 로고
    • note
    • 3B (2 equiv, RT, 4 d); compare with ref. [8].
  • 29
    • 0032913898 scopus 로고    scopus 로고
    • For radical C-C bonding reactions via organoboranes, see: C. Ollivier, P. Renaud, Chem. Eur. J. 1999, 5, 1468-1473.
    • (1999) Chem. Eur. J. , vol.5 , pp. 1468-1473
    • Ollivier, C.1    Renaud, P.2
  • 30
    • 85007625369 scopus 로고    scopus 로고
    • note
    • 2D-COSY and NOESY NMR analysis was used to establish the relative stereochemistry of the hydroboration step for systems 1, 8, and 11-13. The monocyclic protected allylic alcohols 1 and 8 had to be converted initially into the corresponding bicyclic acetals (hydroboration, oxidation, p-toluenesulfonic acid catalyzed acetalization).


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.