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Volumn 13, Issue 16, 2002, Pages 1721-1732

Atropisomerism in monopyrroles

Author keywords

[No Author keywords available]

Indexed keywords

3,5 DIMETHYLPYRROLE; ESTER DERIVATIVE; ETHYL 3,5 DIMETHYL 4 (2',2' DIMETHYL 1' IODOPROPYL) 1H PYRROLE 2 CARBOXYLATE; ETHYL 3,5 DIMETHYL 4 [2',2' DIMETHYL 1' (DIETHOXYCARBONYLMETHYL)PROPYL] 1H PYRROLE 2 CARBOXYLATE; ETHYL 3,5 DIMETHYL 4 [2',2' DIMETHYL 1' (METHOXYCARBONYLMETHYL)PROPYL] 1H PYRROLE 2 CARBOXYLATE; ETHYL 3,5 DIMETHYL 4 [2',2' DIMETHYL 1' (TERT BUTOXYCARBONYLMETHYL)PROPYL] 1H PYRROLE 2 CARBOXYLATE; METHYL 3,4 DIMETHYL 4 (2',2' DIMETHYL 1' METHYLTHIOPROPYL) 1H PYRROLE 2 CARBOXYLATE; METHYL 3,5 DIMETHYL 4 (2',2' DIMETHYL 1' IODOPROPYL) 1H PYRROLE 2 CARBOXYLATE; METHYL 3,5 DIMETHYL 4 (2',2' DIMETHYL 1' METHOXYPROPYL) 1H PYRROLE 2 CARBOXYLATE; METHYL 3,5 DIMETHYL 4 [1' (DIISOPROPOXYCARBONYL)METHYL 2',2' DIMETHYLPROPYL] 1H PYRROLE 2 CARBOXYLATE; METHYL 3,5 DIMETHYL 4 [1' (DIMETHOXYCARBONYL)METHYL 2',2' DIMETHYLPROPYL] 1H PYRROLE 2 CARBOXYLATE; METHYL 3,5 DIMETHYL 4 [2',2' DIMETHYL 1' (1'' METHOXYCARBONYLETHYL)PROPYL] 1H PYRROLE 2 CARBOXYLATE; PYRROLE DERIVATIVE; UNCLASSIFIED DRUG;

EID: 0037183399     PISSN: 09574166     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0957-4166(02)00481-0     Document Type: Article
Times cited : (17)

References (15)
  • 2
    • 0002999412 scopus 로고
    • N.L. Allinger, E.L. Eliel, & S.H. Wilen. J. Wiley and Sons
    • Ōki M. Allinger N.L., Eliel E.L., Wilen S.H., Topics in Stereochemistry. 14:1983;1-81 J. Wiley and Sons.
    • (1983) Topics in Stereochemistry , vol.14 , pp. 1-81
    • Oki, M.1
  • 9
    • 0003909854 scopus 로고
    • New York: J. Wiley & Sons
    • Günther H. NMR Spectroscopy. 1994;335-389 J. Wiley & Sons, New York.
    • (1994) NMR Spectroscopy , pp. 335-389
    • Günther, H.1
  • 11
    • 0005171848 scopus 로고    scopus 로고
    • note
    • An alternative mechanism was suggested in review. Interconversion of diastereomers might also be achieved in 1 by a dissociative mechanism rather than simple C-C bond isomerization. The dissociation mechanism would also require C(4)-C(1′) bond rotation - or recombination with inversion at C(1′).


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.