메뉴 건너뛰기




Volumn 51, Issue 10, 2003, Pages 3056-3059

Is the negative charge on RNHSO3-M+ an essential requirement for sulfamate sweetness?

Author keywords

Bitterness; Cyclamates; Esters; Sulfamates; Sweetness

Indexed keywords

CYCLAMATE SODIUM; SULFAMIC ACID DERIVATIVE; SWEETENING AGENT; UNCLASSIFIED DRUG; ANION; SULFAMIC ACID; SULFONIC ACID DERIVATIVE;

EID: 0037732741     PISSN: 00218561     EISSN: None     Source Type: Journal    
DOI: 10.1021/jf025597b     Document Type: Article
Times cited : (6)

References (25)
  • 1
    • 0038048122 scopus 로고    scopus 로고
    • O'Brien Nabors, L., Ed.; Marcel Dekker: New York
    • Bopp, B. A.; Price, P. In Alternative Sweeteners, 3rd ed.; O'Brien Nabors, L., Ed.; Marcel Dekker: New York, 2001; pp 63-85.
    • (2001) Alternative Sweeteners, 3rd Ed. , pp. 63-85
    • Bopp, B.A.1    Price, P.2
  • 2
    • 84872890669 scopus 로고
    • Mathlouthi, M., Kanters, J. A., Birch, G. G., Eds.; Elsevier Applied Science: New York
    • Spillane, W. J. Sweet-Taste Chemoreception; Mathlouthi, M., Kanters, J. A., Birch, G. G., Eds.; Elsevier Applied Science: New York, 1993; pp 283-289.
    • (1993) Sweet-Taste Chemoreception , pp. 283-289
    • Spillane, W.J.1
  • 4
    • 3242715546 scopus 로고
    • Preparation and properties of some N-substituted sulfamic acids
    • Audrieth, L. F.; Sveda, M. Preparation and properties of some N-substituted sulfamic acids. J. Org. Chem. 1944, 39, 89-101.
    • (1944) J. Org. Chem. , vol.39 , pp. 89-101
    • Audrieth, L.F.1    Sveda, M.2
  • 5
    • 0017175603 scopus 로고
    • Structure-activity studies on sulfamate sweeteners
    • Benson, G. A.; Spillane, W. J. Structure-activity studies on sulfamate sweeteners. J. Med. Chem. 1976, 19, 869-872.
    • (1976) J. Med. Chem. , vol.19 , pp. 869-872
    • Benson, G.A.1    Spillane, W.J.2
  • 6
    • 0020009260 scopus 로고
    • Structure-reactivity relationships in the sweetening cyclamate series: Different N-cyclohexyl sulfamic acid derivatives (esters and amides) as a probe for the corformational requirements of the target sweet taste receptor
    • Pautet, F.; Kamoun, N.; Daudon, M. Structure-reactivity relationships in the sweetening cyclamate series: different N-cyclohexyl sulfamic acid derivatives (esters and amides) as a probe for the corformational requirements of the target sweet taste receptor. Pharm. Acta Helv. 1982, 57, 205-208.
    • (1982) Pharm. Acta Helv. , vol.57 , pp. 205-208
    • Pautet, F.1    Kamoun, N.2    Daudon, M.3
  • 7
    • 0022491566 scopus 로고
    • Specific role of the aminosulfonate group in the interaction of sulfamates with sweetening characteristics with their receptor site
    • Pautet, F.; Daudon, M. Specific role of the aminosulfonate group in the interaction of sulfamates with sweetening characteristics with their receptor site. Pharm. Acta Helv. 1986, 61, 215-217.
    • (1986) Pharm. Acta Helv. , vol.61 , pp. 215-217
    • Pautet, F.1    Daudon, M.2
  • 8
    • 0038724719 scopus 로고
    • Synthesis with N,N′-disubstituted sulfamides. V. Nitration and nitrosylation of 1,3-disubstituted sulfuryl diamides-New synthesis of the little known alkyl amidosulfate
    • Sowada, R. Synthesis with N,N′-disubstituted sulfamides. V. Nitration and nitrosylation of 1,3-disubstituted sulfuryl diamides-New synthesis of the little known alkyl amidosulfate. J. Prakt. Chem. 1965, 29, 328-336.
    • (1965) J. Prakt. Chem. , vol.29 , pp. 328-336
    • Sowada, R.1
  • 10
    • 0009272255 scopus 로고
    • Monoalkylsulfamyl chlorides
    • Hansen, N. C. Monoalkylsulfamyl chlorides. Acta Chem. Scand. 1963, 17, 2141-2142.
    • (1963) Acta Chem. Scand. , vol.17 , pp. 2141-2142
    • Hansen, N.C.1
  • 11
    • 0010575926 scopus 로고
    • Production and reactions of monoalkyl-sulfonyl chlorides
    • Weiss, G.; Schulze, G. Production and reactions of monoalkyl-sulfonyl chlorides. Justus Liebigs Ann. Chem. 1969, 729, 40-51.
    • (1969) Justus Liebigs Ann. Chem. , vol.729 , pp. 40-51
    • Weiss, G.1    Schulze, G.2
  • 12
    • 0037710373 scopus 로고    scopus 로고
    • N-Alkylsulfamoyl chlorides. Belgian Patent 667,311, 1966
    • Weiss, G.; Schulze, G. N-Alkylsulfamoyl chlorides. Belgian Patent 667,311, 1966.
    • Weiss, G.1    Schulze, G.2
  • 13
    • 33847797810 scopus 로고
    • An improved synthesis of sulfamoyl chlorides
    • Kloek, J. A.; Leschinsky, K. L. An improved synthesis of sulfamoyl chlorides. J. Org. Chem. 1976, 41, 4028-4029.
    • (1976) J. Org. Chem. , vol.41 , pp. 4028-4029
    • Kloek, J.A.1    Leschinsky, K.L.2
  • 16
    • 33847086479 scopus 로고
    • Sulfamic acid and its N-substituted derivatives
    • Benson, G. A.; Spillane, W. J. Sulfamic acid and its N-substituted derivatives. Chem. Rev. 1980, 80, 151-186.
    • (1980) Chem. Rev. , vol.80 , pp. 151-186
    • Benson, G.A.1    Spillane, W.J.2
  • 21
    • 37049130332 scopus 로고
    • Hydrolysis of aryl N-methylaminosulfonates: Evidence consistent with an E1cB mechanism
    • Williams, A.; Douglas, K. T. Hydrolysis of aryl N-methylaminosulfonates: Evidence consistent with an E1cB mechanism. J. Chem. Soc., Perkin Trans. 2 1974, 1727-1732.
    • (1974) J. Chem. Soc., Perkin Trans. 2 , pp. 1727-1732
    • Williams, A.1    Douglas, K.T.2
  • 22
    • 84985490861 scopus 로고
    • Aminolysis and hydrolysis of sulphamate esters: Substantial N=S bonding in the transition state leading to N=sulfonylamines
    • Spillane, W. J.; Hogan, G.; McGrath, P. Aminolysis and hydrolysis of sulphamate esters: Substantial N=S bonding in the transition state leading to N=sulfonylamines. J. Phys. Org. Chem. 1995, 8, 610-616.
    • (1995) J. Phys. Org. Chem. , vol.8 , pp. 610-616
    • Spillane, W.J.1    Hogan, G.2    McGrath, P.3


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.