Efficient atom economic approaches towards macrocyclic crown diamides via ring-closing metathesis

Tetrahedron Letters

Volumn 43, Issue 36, 2002, Pages 6421-6426

  Behbehani, Haider ^a   Ibrahim, Maher R ^a   Ibrahim, Yehia A ^a  

^a KUWAIT UNIVERSITY   (Kuwait)

Author keywords

1, dienes; Bis o allyloxyanilides; Bis o allyloxybenzamides; Dibenzodioxadiazacycloalkenediones; Pentabenzodiazatetraoxacycloalkenediones; Ring closing metathesis; Tetrabenzodiazatetraoxacycloalkenediones; Tribenzodioxadiazacycloalkenediones

Indexed keywords

ALKADIENE; DIAMIDE; MACROCYCLIC COMPOUND;

ARTICLE; ATOM; CARBON NUCLEAR MAGNETIC RESONANCE; CATALYST; CONFORMATION; CYCLIZATION; GAS CHROMATOGRAPHY; ISOMER; MASS SPECTROMETRY; PROTON NUCLEAR MAGNETIC RESONANCE; RING CLOSING METATHESIS; SYNTHESIS;

EID: 0037009702     PISSN: 00404039     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0040-4039(02)01379-5     Document Type: Article

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44. 2), 112.4 (CH), 121.4 (C), 121.9 (CH), 124.3 (CH), 125.4 (CH), 129.4 (CH), 129.6 (C), 133.0 (CH), 133.1 (CH), 155.4 (C), 163.7 (C=O).
45. 2 at δ 5.3 and hence getting the molar ratio which can then be converted into percent based on the original molar amount of the starting materials.