{"title":"Recent Progress in the Diverse Synthetic Approaches to Phytosphingosine","authors":"Hangyu Bai, Shuguang Yang, Zhaoyu Wang, Yisheng Zhao, Ying Xu, Yanxin Zhang","doi":"10.1007/s41061-025-00518-8","DOIUrl":null,"url":null,"abstract":"<div><p>Phytosphingosine, a type of sphingolipids, has gained significant attention due to their diverse biological activities, including anti-inflammatory, anticancer, and immunomodulatory properties. These bioactive lipids, predominantly found in plant sources, play crucial roles in cellular signaling and membrane structure. In recent years, the chemical synthesis of phytosphingosine and other sphingolipids have become a major focus in organic chemistry due to the increasing demand for these molecules in pharmacological research and drug development. The synthesis of sphingosine has been extensively reported and is relatively straightforward to implement. However, the synthesis of phytosphingosine is more complex due to the presence of additional chiral centers, leading to a greater diversity of synthetic methods. This review provides a comprehensive overview of the recent advancements in synthetic methodologies for phytosphingosine and its analogs, including asymmetric synthesis and total synthesis using chiral auxiliaries and catalysts. By summarizing recent chemical synthesis advancements, this review serves as a valuable resource for researchers interested in the biological activities and synthetic aspects of phytosphingosine and other sphingolipids.</p></div>","PeriodicalId":802,"journal":{"name":"Topics in Current Chemistry","volume":"383 3","pages":""},"PeriodicalIF":8.8000,"publicationDate":"2025-08-31","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Topics in Current Chemistry","FirstCategoryId":"92","ListUrlMain":"https://link.springer.com/article/10.1007/s41061-025-00518-8","RegionNum":2,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"Chemistry","Score":null,"Total":0}
引用次数: 0
Abstract
Phytosphingosine, a type of sphingolipids, has gained significant attention due to their diverse biological activities, including anti-inflammatory, anticancer, and immunomodulatory properties. These bioactive lipids, predominantly found in plant sources, play crucial roles in cellular signaling and membrane structure. In recent years, the chemical synthesis of phytosphingosine and other sphingolipids have become a major focus in organic chemistry due to the increasing demand for these molecules in pharmacological research and drug development. The synthesis of sphingosine has been extensively reported and is relatively straightforward to implement. However, the synthesis of phytosphingosine is more complex due to the presence of additional chiral centers, leading to a greater diversity of synthetic methods. This review provides a comprehensive overview of the recent advancements in synthetic methodologies for phytosphingosine and its analogs, including asymmetric synthesis and total synthesis using chiral auxiliaries and catalysts. By summarizing recent chemical synthesis advancements, this review serves as a valuable resource for researchers interested in the biological activities and synthetic aspects of phytosphingosine and other sphingolipids.
期刊介绍:
Topics in Current Chemistry provides in-depth analyses and forward-thinking perspectives on the latest advancements in chemical research. This renowned journal encompasses various domains within chemical science and their intersections with biology, medicine, physics, and materials science.
Each collection within the journal aims to offer a comprehensive understanding, accessible to both academic and industrial readers, of emerging research in an area that captivates a broader scientific community.
In essence, Topics in Current Chemistry illuminates cutting-edge chemical research, fosters interdisciplinary collaboration, and facilitates knowledge-sharing among diverse scientific audiences.