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Volumn 688, Issue 1-2, 2003, Pages 273-279

Synthesis of tricarbonyl η6- and η5- [(3-thiophenyl)organo]chromium and -manganese complexes

Author keywords

Chromium; Stille cross coupling; Thiophenyl

Indexed keywords

CHROMIUM DERIVATIVE; MANGANESE DERIVATIVE; ORGANOMETALLIC COMPOUND; PROTON; TRICARBOXYLIC ACID;

EID: 0242607020     PISSN: 0022328X     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.jorganchem.2003.09.030     Document Type: Article
Times cited : (11)

References (28)
  • 18
    • 0242540771 scopus 로고    scopus 로고
    • 6-[(2-thiophenyl)arene]chromium complex was obtained in a low 7% yield. Although the 3-substituted analogue is described, no yield has been indicated by the authors [1a]
    • 6-[(2-thiophenyl)arene]chromium complex was obtained in a low 7% yield. Although the 3-substituted analogue is described, no yield has been indicated by the authors [1a].
  • 19
    • 0038157007 scopus 로고    scopus 로고
    • Complexes 1a, 1b, 4a and 4b have been used as starting material for the synthesis of new chiral heterobimetallic Cr-Ru complexes by regioselective insertion of Ru into the C-S bond
    • Complexes 1a, 1b, 4a and 4b have been used as starting material for the synthesis of new chiral heterobimetallic Cr-Ru complexes by regioselective insertion of Ru into the C-S bond: Giner Planas J. Prim D. Rose-Munch F. Rose E. Thouvenot R. Vaissermann J. Organometallics 21 2002 4385
    • (2002) Organometallics , vol.21 , pp. 4385
    • Giner Planas, J.1    Prim, D.2    Rose-Munch, F.3    Rose, E.4    Thouvenot, R.5    Vaissermann, J.6
  • 21
    • 0028335669 scopus 로고
    • Deshielding effects were observed for the six-membered ring protons in free substituted phenylthiophenes see
    • Deshielding effects were observed for the six-membered ring protons in free substituted phenylthiophenes see: Kirsch G. Prim D. Synth. Commun. 24 1994 1721
    • (1994) Synth. Commun. , vol.24 , pp. 1721
    • Kirsch, G.1    Prim, D.2
  • 22
    • 0242540769 scopus 로고    scopus 로고
    • For a more convenient reading of NMR data, we adopted an atom numbering different from the ortep figures, using H2 for meta-proton with respect to the MeO substituent in all cases, see Scheme 4
    • For a more convenient reading of NMR data, we adopted an atom numbering different from the ortep figures, using H2 for meta-proton with respect to the MeO substituent in all cases, see Scheme 4.
  • 25
    • 0036262798 scopus 로고    scopus 로고
    • 6-arene)tricarbonylchromiuin complexes see, for example
    • 6-arene)tricarbonylchromiuin complexes see, for example, Rose-Munch F. Rose E. Eur. J. Inorg. Chem. 2002 1269
    • (2002) Eur. J. Inorg. Chem. , pp. 1269
    • Rose-Munch, F.1    Rose, E.2
  • 28
    • 0242457171 scopus 로고
    • shelxs-86, Program for Crystal Structure Solution, University of Göttingen, Göttingen, Germany
    • G.M. Sheldrick, shelxs-86, Program for Crystal Structure Solution, University of Göttingen, Göttingen, Germany, 1986.
    • (1986)
    • Sheldrick, G.M.1


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.