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Volumn 55, Issue 1, 1999, Pages 201-210

Reaction of mesoionic compounds deriving from cyclic N-acyl-α- aminoacids with N-(phenylmethylene)benzenesulfonamide

Author keywords

[No Author keywords available]

Indexed keywords

AMPHOLYTE; BENZENESULFONAMIDE DERIVATIVE; CYCLOPEPTIDE;

EID: 0032927039     PISSN: 00404020     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0040-4020(98)01026-6     Document Type: Article
Times cited : (43)

References (18)
  • 3
    • 0028153128 scopus 로고
    • Only the N-benzoyl derivative of 1,3-oxazolidine-4-carboxylic acid is known: Any attempt to synthesize the N-acetyl derivative was unsuccessful
    • Only the N-benzoyl derivative of 1,3-oxazolidine-4-carboxylic acid is known: Conti, S.; Cossu, S.; Giacomelli, G.; Falorni, M. Tetrahedron 1994, 50, 13493. Any attempt to synthesize the N-acetyl derivative was unsuccessful.
    • (1994) Tetrahedron , vol.50 , pp. 13493
    • Conti, S.1    Cossu, S.2    Giacomelli, G.3    Falorni, M.4
  • 10
    • 0013514642 scopus 로고    scopus 로고
    • 1 we repeated the reaction of 1a,b with 5 in toluene solution and acetic anhydride as dehydrating agent
    • 1 we repeated the reaction of 1a,b with 5 in toluene solution and acetic anhydride as dehydrating agent.
  • 11
    • 0013514444 scopus 로고    scopus 로고
    • The reversed regioisomer should show only N.O.E. effect between H-5 and the ortho protons of the C-3 phenyl ring. The assignment of the ortho protons of the two phenyl rings is a consequence of the observed N.O.E. effects with the independently assigned H-5 and H-8
    • The reversed regioisomer should show only N.O.E. effect between H-5 and the ortho protons of the C-3 phenyl ring. The assignment of the ortho protons of the two phenyl rings is a consequence of the observed N.O.E. effects with the independently assigned H-5 and H-8.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.