Selective amination of the mucohalic acid derivatives
摘要:
An efficient synthesis of 4,5-diamino-3-halofuran-2(5H)-ones has been developed based on a sequential acylation and bisamination of mucohalic acids. The beta- and gamma-amination products have also been prepared with high regioselectivity. This reaction shows some advantages in terms of its simple operation and readily available but highly functionalized starting material. All products gave satisfactory IR, H-1 NMR, C-13 NMR and HRMS. (C) 2013 Xue-Qiang Li. Published by Elsevier B.V. on behalf of Chinese Chemical Society. All rights reserved.
An efficient synthesis of 4,5-diamino-3-halofuran-2(5H)-ones has been developed based on a sequential acylation and bisamination of mucohalic acids. The beta- and gamma-amination products have also been prepared with high regioselectivity. This reaction shows some advantages in terms of its simple operation and readily available but highly functionalized starting material. All products gave satisfactory IR, H-1 NMR, C-13 NMR and HRMS. (C) 2013 Xue-Qiang Li. Published by Elsevier B.V. on behalf of Chinese Chemical Society. All rights reserved.