Methods for preparation of macrocyclic molecules and macrocyclic molecules prepared thereby
申请人:The President and Fellows of Harvard College
公开号:US20020192773A1
公开(公告)日:2002-12-19
The preparation of macrocyclic molecules from linear, synthetic thioester precursors is disclosed. An excised thioesterase domain isolated from either a PKS or NRPS multidomain system catalyzes the cyclization reaction. Thioester substrates also are described that are efficiently cyclized by the method of the present invention. Additionally, macrocyclic molecules, including macrolactones and macrolactams, that are prepared by the macrocyclization methods of the invention are described.
本研究公开了从线性合成硫酯前体制备大环分子的方法。从 PKS 或 NRPS 多域系统中分离出来的切除硫酯酶结构域可催化环化反应。本发明还描述了可通过本发明方法高效环化的硫酯底物。此外,还介绍了通过本发明的大环化方法制备的大环分子,包括大内酯和大内酰胺。