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Volumn 3, Issue 8, 2001, Pages 1137-1140

Enantioselective oxidative biaryl coupling reactions catalyzed by 1,5-diazadecalin metal complexes

Author keywords

[No Author keywords available]

Indexed keywords

1,5 DIAZADECALIN; 1,5-DIAZADECALIN; COPPER; CUPROUS IODIDE; DECALIN; FUSED HETEROCYCLIC RINGS; IODIDE; LIGAND; NAPHTHALENE DERIVATIVE; OXYGEN; PIPERIDINE DERIVATIVE; WATER;

EID: 0035912345     PISSN: 15237060     EISSN: None     Source Type: Journal    
DOI: 10.1021/ol015595x     Document Type: Article
Times cited : (236)

References (45)
  • 7
    • 0000718373 scopus 로고    scopus 로고
    • (a) Pu, L. Chem. Rev. 1998, 98, 2405-2494.
    • (1998) Chem. Rev. , vol.98 , pp. 2405-2494
    • Pu, L.1
  • 11
    • 0001073559 scopus 로고
    • For a review of biaryl bond forming methods, see: Sainsbury, M. Tetrahedron 1980, 36, 3327-3359.
    • (1980) Tetrahedron , vol.36 , pp. 3327-3359
    • Sainsbury, M.1
  • 34
    • 0041787943 scopus 로고    scopus 로고
    • note
    • Homogeneous conditions were employed to preclude asymmetric induction via diastereomieric recrystallization as has been reported for some stoichiometric oxidative copper couplings. See refs 8a, 8e, and 9b.
  • 42
    • 0042289019 scopus 로고    scopus 로고
    • note
    • 2) resulted in no further reaction.
  • 43
    • 0042790135 scopus 로고    scopus 로고
    • note
    • The 3-substituent most likely chelates the metal center creating a stereochemically well-defined environment and/or ensuring that the intermediate remains associated with the metal center.
  • 44
    • 0041787944 scopus 로고    scopus 로고
    • note
    • 4, the solvent was removed to provide the crude product (13.4 g) as a reddish brown solid. Treament with MeOH (100 mL) left 8a (8.06 g, 81%, 93% ee) undissolved as a light-brown solid. Additional product (0.21 g. 2%, 98% ee) could be obtained from the MeOH portion after chromatography.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.