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Volumn 5, Issue 24, 2007, Pages 4001-4009

Experimental and computational evidence for α-lactone intermediates in the addition of aqueous bromine to disodium dimethyl-maleate and -fumarate

Author keywords

[No Author keywords available]

Indexed keywords

ADDITION REACTIONS; BROMINE COMPOUNDS; FREE ENERGY; SOLUTIONS; STEREOCHEMISTRY; SYNTHESIS (CHEMICAL); X RAY CRYSTALLOGRAPHY;

EID: 36749044733     PISSN: 14770520     EISSN: None     Source Type: Journal    
DOI: 10.1039/b711538e     Document Type: Article
Times cited : (10)

References (84)
  • 15
    • 0000116076 scopus 로고
    • There has been much recent work on the precise structures involved; see:
    • I. Roberts G. E. Kimball J. Am. Chem. Soc. 1937 59 947 948
    • (1937) J. Am. Chem. Soc. , vol.59 , pp. 947-948
    • Roberts, I.1    Kimball, G.E.2
  • 46
    • 84943008696 scopus 로고    scopus 로고
    • note
    • Although, strictly speaking, this is exo-tet, the geometry of the halonium ion is such that it may be regarded as an endo-trig process; other authors have taken this view (see ref. 19, 29, 37, and 38).
  • 63
    • 84943008697 scopus 로고    scopus 로고
    • note
    • The observation that bromination of diethyl maleate using aqueous bromine and added bromide ions affords the meso dibromide (i.e. syn addition) (see ref. 53) can be accounted for by isomerisation of diethyl maleate into diethyl fumarate under these conditions (see ref. 54).
  • 79
    • 85162619565 scopus 로고
    • E. Ott Ber. 1928 61 2124 2142
    • (1928) Ber. , vol.61 , pp. 2124-2142
    • Ott, E.1
  • 84
    • 84943005926 scopus 로고    scopus 로고
    • Chemical Computing Group, 1010 Sherbrooke Street, Suite 910, Montreal, Quebec, Canada
    • MOE 2004.03 Software, Chemical Computing Group, 1010 Sherbrooke Street, Suite 910, Montreal, Quebec, Canada
    • MOE 2004.03 Software


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.