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Volumn 9, Issue 12, 2003, Pages 2789-2796

Substrate-controlled highly diastereoselective synthesis of primary and secondary diorganozinc reagents by a hydroboration/boron - Zinc exchange sequence

Author keywords

C C coupling; Diastereoselective synthesis; Hydroboration; Transmetallation; Zinc organometallics

Indexed keywords

BORON; SUBSTRATES; SYNTHESIS (CHEMICAL); ZINC;

EID: 0038452352     PISSN: 09476539     EISSN: None     Source Type: Journal    
DOI: 10.1002/chem.200204662     Document Type: Article
Times cited : (37)

References (43)
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    • a) D. Männig, H. Nöth, Angew. Chem. 1985, 97, 854; Angew. Chem. Int. Ed. Engl. 1985, 24, 878;
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    • a) D. Männig, H. Nöth, Angew. Chem. 1985, 97, 854; Angew. Chem. Int. Ed. Engl. 1985, 24, 878;
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  • 25
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    • Asymmetric hydroborations using a chiral catalyst and subsequent boron-zinc exchange reaction did not lead to the corresponding optically active benzylic diorganozinc reagent; it seems that this benzylic zinc reagent is not configurationally stable under the reaction conditions applied; see also: E. Fernandez, K. Maeda, M. W. Hooper, J. M. Brown, Chem. Eur. J. 2000, 6, 1840.
    • (2000) Chem. Eur. J. , vol.6 , pp. 1840
    • Fernandez, E.1    Maeda, K.2    Hooper, M.W.3    Brown, J.M.4
  • 28
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    • a) The reported conditions for the hydroboration (3 equiv of catecholborane) were used to ensure the reproducibility of selectivities. D. A. Evans, G. C. Fu, A. H. Hoveyda, J. Am. Chem. Soc. 1988, 110, 6917;
    • (1988) J. Am. Chem. Soc. , vol.110 , pp. 6917
    • Evans, D.A.1    Fu, G.C.2    Hoveyda, A.H.3
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    • note
    • 2.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.