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Volumn 64, Issue 18, 2008, Pages 3953-3959

Diastereoselective addition of organozinc and organomagnesium reagents to 2-(2′-pyrimidyl)ferrocenecarbaldehyde

Author keywords

Addition reactions; Asymmetric synthesis; Metallocenes; Organometallic reagents; Stereoselectivity

Indexed keywords

2 (2' PYRIMIDYL)FERROCENECARBALDEHYDE; ALDEHYDE DERIVATIVE; ORGANOMAGNESIUM; ORGANOMETALLIC COMPOUND; ORGANOZINC; REAGENT; UNCLASSIFIED DRUG;

EID: 40849123868     PISSN: 00404020     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.tet.2008.02.056     Document Type: Article
Times cited : (9)

References (55)
  • 8
    • 40849138216 scopus 로고    scopus 로고
    • See, inter alia:
    • See, inter alia:
  • 21
    • 40849150917 scopus 로고    scopus 로고
    • For other additions to aldehyde 5, see:
    • For other additions to aldehyde 5, see:
  • 24
    • 40849141281 scopus 로고    scopus 로고
    • Reviews:
    • Reviews:
  • 31
    • 40849115146 scopus 로고    scopus 로고
    • For related reactions, see:
    • For related reactions, see:
  • 34
    • 0037031630 scopus 로고    scopus 로고
    • Readily obtained from 2-chloropyrimidine as described in:
    • Readily obtained from 2-chloropyrimidine as described in:. Vlád G., and Horváth I.T. J. Org. Chem. 67 (2002) 6550
    • (2002) J. Org. Chem. , vol.67 , pp. 6550
    • Vlád, G.1    Horváth, I.T.2
  • 37
    • 40849089435 scopus 로고    scopus 로고
    • note
    • 2=0.1265. Crystallographic data (excluding structure factors) for this structure have been deposited with the Cambridge Crystallographic Data Centre as supplementary publication no CCDC-663416. Copies of the data can be obtained, free of charge, on application to The Cambridge Crystallographic Data Centre, 12 Union Road, Cambridge CB2 1EZ, UK, (fax: +44 (0)1223 336033 or e-mail: deposit@ccdc.cam.ac.uk).
  • 38
    • 40849120242 scopus 로고    scopus 로고
    • note
    • 13
  • 45
    • 1942532912 scopus 로고    scopus 로고
    • Rapid intramolecular alkyl transfer in a chelated intermediate has been previously proposed for the fast, highly diastereoselective addition of dialkylzinc reagents to atropisomeric 2-formyl arylamides:
    • Rapid intramolecular alkyl transfer in a chelated intermediate has been previously proposed for the fast, highly diastereoselective addition of dialkylzinc reagents to atropisomeric 2-formyl arylamides:. Jimeno C., Rios R., Carroll P.J., and Walsh P.J. Tetrahedron 60 (2004) 4543
    • (2004) Tetrahedron , vol.60 , pp. 4543
    • Jimeno, C.1    Rios, R.2    Carroll, P.J.3    Walsh, P.J.4
  • 46
    • 40849120241 scopus 로고    scopus 로고
    • note
    • -1, respectively).
  • 47
    • 40849139746 scopus 로고    scopus 로고
    • note
    • ® package of programs.
  • 48
    • 40849106910 scopus 로고    scopus 로고
    • note
    • 18 suitable for the intramolecular transfer of an alkyl group.
  • 50
    • 40849088397 scopus 로고    scopus 로고
    • For the application of structurally related (2-substituted) ferrocenylcarbinols as chiral ligands in asymmetric catalysis, see inter alia:
    • For the application of structurally related (2-substituted) ferrocenylcarbinols as chiral ligands in asymmetric catalysis, see inter alia:


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.