Department of Organic Chemistry, Belarusian State University, Leningradskaya 14, 220050 Minsk, Belarus.
Department of Chemistry and Biotechnology, School of Science, Tallinn University of Technology, Akadeemia tee 15, 12618 Tallinn, Estonia.
Molecules. 2020 Dec 30;26(1):140. doi: 10.3390/molecules26010140.
Oxidative fragmentation of tertiary cyclopropanols with phenyliodine(III) dicarboxylates in aprotic solvents (dichloromethane, chloroform, toluene) produces mixed anhydrides. The fragmentation reaction is especially facile with phenyliodine(III) reagents bearing electron-withdrawing carboxylate ligands (trifluoroacetyl, 2,4,6-trichlorobenzoyl, 3-nitrobenzoyl), and affords 95-98% yields of the corresponding mixed anhydride products. The latter can be straightforwardly applied for the acylation of various nitrogen, oxygen and sulfur-centered nucleophiles (primary and secondary amines, hydroxylamines, primary alcohols, phenols, thiols). Intramolecular acylation yielding macrocyclic lactones can also be performed. The developed transformation has bolstered the synthetic utility of cyclopropanols as pluripotent intermediates in diversity-oriented synthesis of bioactive natural products and their synthetic congeners. For example, it was successfully applied for the last-stage modification of a cyclic peptide to produce a precursor of a known histone deacetylase inhibitor.
在非质子溶剂(二氯甲烷、氯仿、甲苯)中,用苯碘酰基二酸酯氧化断裂叔环丙醇生成混合酸酐。带有吸电子羧酸酯配体(三氟乙酰基、2,4,6-三氯苯甲酰基、3-硝基苯甲酰基)的苯碘酰基试剂使断裂反应特别容易进行,得到相应混合酸酐产物的产率为 95-98%。后者可直接用于各种氮、氧和硫中心亲核试剂(伯胺和仲胺、羟胺、伯醇、酚、硫醇)的酰化。也可以进行分子内酰化生成大环内酯。开发的转化增强了环丙醇作为多样性导向合成生物活性天然产物及其合成类似物中多能中间体的合成实用性。例如,它成功地应用于环状肽的最后阶段修饰,生成已知组蛋白去乙酰化酶抑制剂的前体。