Improving the efficiency of forming 'unfavorable' products: Eight-residue macrocycles from folded aromatic oligoamide precursors

Synlett

Volumn , Issue 9, 2009, Pages 1437-1440

  Zou, Shuliang ^a   He, Youzhou ^a   Yang, Yongan ^a   Zhao, Yi ^a   Yuan, Lihua ^a   Feng, Wen ^a   Yamato, Kazuhiro ^b   Gong, Bing ^b  

^a SICHUAN UNIVERSITY   (China)

^b UNIVERSITY AT BUFFALO   (United States)

Author keywords

Cyclizations; Folding oligoamides; Hydrogen bonds; Macrocycles; Synthesis

Indexed keywords

AMIDE; BENZENE DERIVATIVE; DIAMINE;

ARTICLE; CHEMICAL REACTION; CHEMICAL STRUCTURE; CYCLIZATION; HYDROGEN BOND; MATRIX ASSISTED LASER DESORPTION IONIZATION TIME OF FLIGHT MASS SPECTROMETRY; PROTON NUCLEAR MAGNETIC RESONANCE; SYNTHESIS; TEMPERATURE MEASUREMENT;

EID: 67649321677     PISSN: 09365214     EISSN: 14372096     Source Type: Journal    
DOI: 10.1055/s-0029-1217173     Document Type: Article

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27. 3N in 0.5 h. The mxiture was stirred 6 h. After washing with 10% HCl, the residue was recrystallized several times from acetone to provide 4c in 40% yield.