A closer look on various synthetic routes to Callystatin A: a cytotoxic marine sponge polyketide

Q2 Chemistry
Aamer Saeed, Babar Hussain Shah, Rabia Qamar
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引用次数: 0

Abstract

Callystatin A, a polyketide marine natural product, has been known since 1997 after its isolation from the sponge Callyspongia truncata by Kobayashi et al. It belongs to the leptomcyin family of natural products with a highly conjugated and stereodefined skeleton. The challenging structural topographies and remarkable anti-proliferative properties of (−)-Callystatin A stimulated many researchers to pursue the total synthesis of this marine polyketide. This review is exclusively focused on the research undertaken towards the concise, asymmetric total synthesis of Callystatin A over the last two decades. The various target oriented synthetic pathways are discussed in a chronological order to give a comprehensive overview.

Abstract Image

Callystatin A:一种具有细胞毒性的海绵聚酮
Callystatin A是1997年由Kobayashi等人从海绵Callyspongia truncata中分离得到的一种聚酮类海洋天然产物。它属于瘦细胞素家族的天然产物,具有高度共轭和立体定义的骨架。(−)-Callystatin A具有挑战性的结构地形和显著的抗增殖特性,促使许多研究人员追求这种海洋聚酮的全合成。这篇综述是专门针对在过去的二十年中对Callystatin A的简洁,不对称的全合成所进行的研究。各种面向目标的合成途径是讨论在时间顺序给出一个全面的概述。
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来源期刊
Tetrahedron, asymmetry
Tetrahedron, asymmetry 化学-无机化学与核化学
CiteScore
4.70
自引率
0.00%
发文量
0
审稿时长
1 months
期刊介绍: Cessation. Tetrahedron: Asymmetry presents experimental or theoretical research results of outstanding significance and timeliness on asymmetry in organic, inorganic, organometallic and physical chemistry, as well as its application to related disciplines, especially bio-organic chemistry. The journal publishes critical reviews, original research articles and preliminary communications dealing with all aspects of the chemical, physical and theoretical properties of non-racemic organic and inorganic materials and processes. Topics relevant to the journal include: the physico-chemical and biological properties of enantiomers; strategies and methodologies of asymmetric synthesis; resolution; chirality recognition and enhancement; analytical techniques for assessing enantiomeric purity and the unambiguous determination of absolute configuration; and molecular graphics and modelling methods for interpreting and predicting asymmetric phenomena. Papers describing the synthesis or properties of non-racemic molecules will be required to include a separate statement in the form of a Stereochemistry Abstract, for publication in the same issue, of the criteria used for the assignment of configuration and enantiomeric purity.
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