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Volumn , Issue 8, 2005, Pages 1350-1358

Acylurea pyrolysis - Thermolysis of N,N′-disubstituted ferrocenoylureas as a new way to N-monosubstituted ferrocenecarboxamides

Author keywords

Acylurea; Amide; DCC; Ferrocene; Peptide bond; Pyrolysis; Urea

Indexed keywords

CARBOXYLIC ACIDS; CRYSTAL STRUCTURE; IRON COMPOUNDS; REACTION KINETICS; SINGLE CRYSTALS; SUBSTITUTION REACTIONS; SYNTHESIS (CHEMICAL); UREA;

EID: 20344399643     PISSN: 00397881     EISSN: None     Source Type: Journal    
DOI: 10.1055/s-2005-865286     Document Type: Article
Times cited : (5)

References (66)
  • 5
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    • (1997) Naturstoffchemie , pp. 157
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  • 19
    • 0000416726 scopus 로고
    • (a) According to the statement of one of the referees ferrocenoyl acid chloride is easily accessible by treatement of ferrocenecarboxylic acid with oxalyl chloride in large yield. This is in agreement with the results of Lorkowski et al.: Lorkowski, H.-J.; Pannier, R.; Wende, A. J. Prakt. Chem. 1967, 35, 149.
    • (1967) J. Prakt. Chem. , vol.35 , pp. 149
    • Lorkowski, H.-J.1    Pannier, R.2    Wende, A.3
  • 30
    • 1842772956 scopus 로고    scopus 로고
    • While this work was in progress Dr. Imrie, Port Elizabeth, informed us by a personal communication that he had synthesized independently from us this species in the same way, by the method described by Wang and Huang: Wang, Q. M.; Huang, R. Q. J. Chem. Res., Synop. 2001, 246.
    • (2001) J. Chem. Res., Synop. , pp. 246
    • Wang, Q.M.1    Huang, R.Q.2
  • 65
    • 0004150157 scopus 로고    scopus 로고
    • Universität Göttingen: Germany
    • Sheldrick, G. M. SHELX-97; Universität Göttingen: Germany, 1997.
    • (1997) SHELX-97
    • Sheldrick, G.M.1
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    • note
    • A scale-up was tried for the synthesis of C1. The reaction was carried out with A1 (2 g) in refluxing dioxane (50 mL). No decrease of the yield was detectable and unconverted A1 could be easily recovered. The yield was 63%.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.