A convenient [2+2] cycloaddition–cycloreversion reaction for the synthesis of 1,1-dicyanobuta-1,3-diene-scaffolded peptides as new imaging chromophores
作者:Dirk T.S. Rijkers、Fernando de Prada López、Rob M.J. Liskamp、François Diederich
DOI:10.1016/j.tetlet.2011.10.084
日期:2011.12
reactive electron-rich Nα-(4-ethynylphenyl)-Nα-(methyl)-glycyl- and an electron-deficient [4-(2,2-dicyanovinyl)]benzoyl moiety. The resulting donor-substituted 1,1-dicyanobuta-1,3-dienes represent a new class of orange-red colored (λmax = 450–500 nm, with molar extinction coefficients (ε) above 5,000 mol−1 dm3 cm−1) peptide-based imaging chromophores.
我们在具有相互反应的富电子官能无色肽片段之间的化学选择性耦合报告Ñ α(4-乙炔基苯基) - - ñ α - (甲基)-glycyl-和缺电子[4-(2,2-二氰基乙烯基)]苯甲酰基部分。将得到的供体-取代的1,1- dicyanobuta -1,3-二烯代表一类新的桔红色着色(λ最大 = 450-500纳米,具有摩尔消光系数(ε以上5000摩尔)-1 分米3 厘米- 1)基于肽的成像生色团。