Strategies for the construction of γ-spirocyclic butenolides in natural product synthesis

被引：42

作者：

Mandal, Sudip ^{[1
]}

Thirupathi, Barla ^{[1
]}

机构：

[1] Indian Inst Sci Educ & Res Berhampur, Dept Chem Sci, Transit Campus,Govt ITI Bldg,NH 59,Engn Sch Rd, Berhampur 760010, Odisha, India

来源：

ORGANIC & BIOMOLECULAR CHEMISTRY | 2020年 / 18卷 / 28期

关键词：

VINYLOGOUS MANNICH REACTIONS; ANTI-TUMOR ANTIBIOTICS; CYTOTOXIC STYRYL-LACTONES; RECEPTOR ANTAGONIST; ASYMMETRIC-SYNTHESIS; ABYSSOMICIN-C; ABSOLUTE STEREOCHEMISTRY; ALKALOIDS RUGULOVASINE; STREPTOMYCES SP-NR0489; SELECTIVE SYNTHESIS;

D O I：

10.1039/d0ob00954g

中图分类号：

O62 [有机化学];

学科分类号：

070303 ; 081704 ;

摘要：

Over the last four decades, a number of gamma-spirocyclic butenolide containing natural products, drugs, and medicinally useful synthetic compounds have been reported. In this review, we discuss diverse chemical approaches to synthesize gamma-spiro butenolides and their application towards natural product synthesis. The collective perception of various methods may allow superior approaches capable of delivering efficient synthetic approaches to obtain gamma-spiro butenolide comprising natural products and their hybrid analogues for further drug discovery and development.

引用

收藏

页码：5287 / 5314

页数：28

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