Knapp Spencer, Yu Younong
Department of Chemistry & Chemical Biology, Rutgers The State University of New Jersey, Piscataway, NJ 08854, USA.
Org Lett. 2007 Mar 29;9(7):1359-62. doi: 10.1021/ol0702472. Epub 2007 Mar 6.
[structure: see text]. Pactamycin, one of the most complex and densely functionalized aminocyclitol antibiotics known, presents synthetic challenges that include reactivity and sterics, relative and absolute stereochemistry, and functional group compatibility and protection. An approach is reported that features four different types of (cyclopentane) face selective functionalization reactions and results in a polyfunctionalized and appropriately protected intermediate that incorporates all the core carbons and the oxygenated functionality of the target.
[结构:见正文]。 pactamycin是已知最复杂且官能团密集的氨基环醇抗生素之一,它带来了包括反应性和空间位阻、相对和绝对立体化学以及官能团兼容性和保护等合成挑战。本文报道了一种方法,其特点是有四种不同类型的(环戊烷)面选择性官能团化反应,并得到一个多官能团化且得到适当保护的中间体,该中间体包含了目标物的所有核心碳原子和含氧官能团。