Unusual “Head-to-Torso” Coupling of Terpene Precursors as a New Strategy for the Structural Diversification of Natural Products

Author(s):  
Robin Teufel
ACS Catalysis ◽  
2021 ◽  
pp. 4670-4681
Author(s):  
Robert M. Hohlman ◽  
Sean A. Newmister ◽  
Jacob N. Sanders ◽  
Yogan Khatri ◽  
Shasha Li ◽  
...  

ChemInform ◽  
2014 ◽  
Vol 45 (4) ◽  
pp. no-no
Author(s):  
Jayprakash Narayan Kumar ◽  
Parigi Raghavendra Reddy ◽  
Biswanath Das ◽  
C. Ganesh Kumar ◽  
Pombala Sujitha

2020 ◽  
Vol 22 (11) ◽  
pp. 4311-4315 ◽  
Author(s):  
Tongxuan Bai ◽  
Yudai Matsuda ◽  
Hui Tao ◽  
Takahiro Mori ◽  
Yonghui Zhang ◽  
...  

2020 ◽  
Vol 18 (2) ◽  
pp. 263-271 ◽  
Author(s):  
Xiaoshuang Gao ◽  
Chengyang Li ◽  
Yao Yuan ◽  
Xiaomin Xie ◽  
Zhaoguo Zhang

Polycyclic indole scaffolds are ubiquitous in pharmaceuticals and natural products and in materials science.


2016 ◽  
Vol 310 (9) ◽  
pp. G629-G644 ◽  
Author(s):  
Roxane Khoogar ◽  
Byung-Chang Kim ◽  
Jay Morris ◽  
Michael J. Wargovich

The last decade has witnessed remarkable progress in the utilization of natural products for the prevention and treatment of human cancer. Many agents now in the pipeline for clinical trial testing have evolved from our understanding of how human nutritional patterns account for widespread differences in cancer risk. In this review, we have focused on many of these promising agents arguing that they may provide a new strategy for cancer control: natural products once thought to be only preventive in their mode of action now are being explored for efficacy in tandem with cancer therapeutics. Natural products may reduce off-target toxicity of therapeutics while making cancers more amenable to therapy. On the horizon is the use of certain natural products, in their own right, as mitigants of late-stage cancer, a new frontier for small-molecule natural product drug discovery.


2020 ◽  
Vol 11 (35) ◽  
pp. 9421-9425
Author(s):  
Oussama Yahiaoui ◽  
Adrian Almass ◽  
Thomas Fallon

A new strategy to the endiandric acid natural products is demonstrated by intercepting the 8π/6π/IMDA pericyclic cascade through a tactical anti-vicinal difunctionalisation of cyclooctatetraene.


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