作者:Young‐Ah Kim、So‐Yeop Han
DOI:10.1081/scc-200026636
日期:2004.1.1
Abstract Chloptosin is an apoptosis‐inducing dimeric cyclohexapeptide. Enantioselective synthesis of L‐6‐chloropyrroloindoline, as the key chiral synthon of the cyclohexapeptide of chloptosin, was successfully achieved starting from 3‐chloroaniline by utilizing Fischer indole/Schöllkopf protocol and oxidative cyclization of resulting L‐6‐chlorotryptophan.
摘要 Chloptosin 是一种诱导细胞凋亡的二聚环六肽。L-6-氯吡咯并二氢吲哚的对映选择性合成是氯酮环六肽的关键手性合成子,从3-氯苯胺开始,利用Fischer吲哚/Schöllkopf方案和所得L-6-氯色氨酸的氧化环化,成功实现了对映选择性合成。