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Volumn 47, Issue 7, 2006, Pages 1055-1058

Reducing properties of 1,2-diaryl-1,2-disodiumethanes

Author keywords

Alkali metals; Dicarbanions; Elimination; Reduction

Indexed keywords

1 PHENYL 2 (2 PYRIDYL) 1,2 DISODIUMETHANE; 1,2 DIPHENYL 2 (2 PYRIDYL) 1,2 DISODIUMETHANE; ALCOHOL; ALKENE; AMIDE; BROMINE DERIVATIVE; CARBOXYLIC ACID; ESTER; METHANE; REDUCING AGENT; UNCLASSIFIED DRUG;

EID: 30544447839     PISSN: 00404039     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.tetlet.2005.12.054     Document Type: Article
Times cited : (7)

References (33)
  • 13
  • 23
    • 30544441796 scopus 로고    scopus 로고
    • note
    • 1H NMR analysis of crude reaction mixtures, to determine the percentage of deuterium incorporation in the arylmethyl positions. See Ref. 4.
  • 25
    • 30544431584 scopus 로고    scopus 로고
    • note
    • 1H NMR to determine the exact amount of trans-stilbazole, this mixture can be successfully recycled to a new reductive dehalogenation reaction.
  • 27
    • 30544450051 scopus 로고
    • Chem. Zentralbl. 106 1935 2358
    • (1935) Chem. Zentralbl. , vol.106 , pp. 2358
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    • (1935) Chem. Abs. , vol.29 , pp. 1062
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    • 30544449328 scopus 로고
    • See also: G. Rankoff Chem. Ber. 63 1930 2139 2142
    • (1930) Chem. Ber. , vol.63 , pp. 2139-2142
    • Rankoff, G.1
  • 30
    • 30544432952 scopus 로고    scopus 로고
    • note
    • Similar results were obtained employing 1a as a reducing agent; however, the employment of 1b allowed an easier purification of reaction products.
  • 31
    • 30544454251 scopus 로고
    • The trans stereochemistry of amide 2f, was assigned by comparison with the stereochemistry of the corresponding N-carboxamide and N-carbonyl chloride, prepared under similar reaction conditions: G. Bellucci, C. Chiappe, F. Marioni, and F. Marchetti J. Chem. Soc., Perkin Trans. 2 1992 637 642 and references cited therein
    • (1992) J. Chem. Soc., Perkin Trans. 2 , pp. 637-642
    • Bellucci, G.1    Chiappe, C.2    Marioni, F.3    Marchetti, F.4
  • 33
    • 30544438446 scopus 로고    scopus 로고
    • note
    • Alternative reductive elimination mechanisms are usually described as 'single electron' or as 'concerted two electrons' reaction pathways. For an in-depth comparison of these mechanisms, see Ref. 5c.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.