메뉴 건너뛰기




Volumn , Issue 11, 2009, Pages 1827-1829

Trifluoromethyl-substituted analogues of 1-aminocyclobutane-1-carboxylic acid

Author keywords

Alkylation; Amino acids; Conformational restriction; Cyclobutane; Fluorine

Indexed keywords

1 AMINO 3,3 BIS(TRIFLUOROMETHYL)CYCLOBUTANAMINIUM CHLORIDE; 1 AMINOCYCLOBUTANECARBOXYLIC ACID; 1 CARBOXY 3 (TRIFLUOROMETHYL)CYCLOBUTANAMINIUM CHLORIDE; 1,3 DIBROMOACETONE DIMETHYL KETAL; ACETAL DERIVATIVE; CYCLOBUTANE; FLUORINE; HYDANTOIN DERIVATIVE; UNCLASSIFIED DRUG;

EID: 67649976811     PISSN: 09365214     EISSN: 14372096     Source Type: Journal    
DOI: 10.1055/s-0029-1217355     Document Type: Article
Times cited : (22)

References (22)
  • 12
    • 67649973369 scopus 로고    scopus 로고
    • WO 2007001940 A2 20070104
    • (c) Goodman, M. M. WO 2007001940 A2 20070104, 2007.
    • (2007)
    • Goodman, M.M.1
  • 19
    • 67649920667 scopus 로고    scopus 로고
    • Bergs, H. DE 566094, 1929; Chem. Abstr. 1933, 27: 1001.
    • (a) Bergs, H. DE 566094, 1929; Chem. Abstr. 1933, 27: 1001.
  • 21
    • 0000184284 scopus 로고    scopus 로고
    • Baasner, B, Hagemann, H, Tatlow, J. C, Eds, Thieme: Stuttgart
    • Dmowski, W. Houben-Weyl Methods of Organic Chemistry, Vol. E10a; Baasner, B.; Hagemann, H.; Tatlow, J. C., Eds.; Thieme: Stuttgart, 1999, 321.
    • (1999) Houben-Weyl Methods of Organic Chemistry , vol.E10a , pp. 321
    • Dmowski, W.1
  • 22
    • 67649995136 scopus 로고    scopus 로고
    • Spectral and Analytical Data for New Compounds Diisopropyl 3-Oxo-1,1-cyclobutanedicarboxylate (10) 1H NMR (400 MHz, CDCl3, δ, 5.10 [m, J, 6.4 Hz, 2 H, CH(CH 3)2, 3.58 (s, 4 H, CH2, 1.26 [d, J, 6.4 Hz, 12 H, CH(CH3)2, 13C NMR (100 MHz, CDCl3, δ, 200.95 (s, CH2CO, 169.64 (s, COO, 69.66 [s, CH(CH3)2, 54.98 (s, CH2CO, 43.54 [s, C(COOi-Pr)2, 21.14 [s, CH(CH3)2, MS: m/z, 243 [M, 1, Diisopropyl 6,8-Dioxo-5,7-diazaspiro[3.4]octane-2,2-dicarboxylate (11) Mp 142-143 °C. 1H NMR (400 MHz, CDCl3, δ, 8.75 (br s, 1 H, NH, 6.69 (s, 1 H, NH, 5.03 [m, 2 H, CH(CH3) 2, 3.14 (d, J, 13.6 Hz, 2 H, CH2, 2.63 d, J, 13.6 Hz, 2
    • 2). MS: m/z = 184 [M -Cl].


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.