Hill Matthew D, Movassaghi Mohammad
Department of Chemistry, Massachusetts Institute of Technology, 77 Massachusetts Avenue, Cambridge MA 02139, USA.
Chemistry. 2008;14(23):6836-44. doi: 10.1002/chem.200800014.
Recent advances in pyrimidine synthesis are described. Modification of conventional strategies involving N-C-N fragment condensation with 1,3-dicarbonyl derivatives remains a common theme in current literature. Other methods, including N-C fragment condensation strategies, provide reactive intermediates capable of intramolecular cyclization and formation of pyrimidine derivatives. These recently developed methodologies offer a valuable addendum to azaheterocycle synthesis.
本文描述了嘧啶合成的最新进展。涉及N-C-N片段与1,3-二羰基衍生物缩合的传统策略的改进仍是当前文献中的一个常见主题。其他方法,包括N-C片段缩合策略,可提供能够进行分子内环化并形成嘧啶衍生物的反应中间体。这些最近开发的方法为氮杂环化合物的合成提供了有价值的补充。