Counting on natural products for drug design
Natural products and their molecular frameworks have a long tradition as valuable starting
points for medicinal chemistry and drug discovery. Recently, there has been a revitalization …
points for medicinal chemistry and drug discovery. Recently, there has been a revitalization …
Strategies to diversify natural products for drug discovery
G Li, HX Lou - Medicinal research reviews, 2018 - Wiley Online Library
Natural product libraries contain specialized metabolites derived from plants, animals, and
microorganisms that play a pivotal role in drug discovery due to their immense structural …
microorganisms that play a pivotal role in drug discovery due to their immense structural …
Prevalence of diarylprolinol silyl ethers as catalysts in total synthesis and patents
GJ Reyes-Rodríguez, NM Rezayee… - Chemical …, 2019 - ACS Publications
Diarylprolinol silyl ethers are among the most utilized stereoselective organocatalysts for the
construction of complex molecules. With their debut in 2005, these catalysts have been …
construction of complex molecules. With their debut in 2005, these catalysts have been …
Synthetic approaches towards alkaloids bearing α-tertiary amines
A Hager, N Vrielink, D Hager, J Lefranc… - Natural product …, 2016 - pubs.rsc.org
Covering: up to August 2015 Alkaloids account for some of the most beautiful and
biologically active natural products. Although they are usually classified along biosynthetic …
biologically active natural products. Although they are usually classified along biosynthetic …
Scaffold diversity synthesis and its application in probe and drug discovery
M Garcia‐Castro, S Zimmermann… - Angewandte Chemie …, 2016 - Wiley Online Library
Scaffold diversity is a crucial feature of compound collections that has a huge impact on their
success in biological screenings. The synthesis of highly complex and diverse scaffolds …
success in biological screenings. The synthesis of highly complex and diverse scaffolds …
Biosynthetically inspired divergent approach to monoterpene indole alkaloids: total synthesis of mersicarpine, leuconodines B and D, leuconoxine, melodinine E …
Inspired by their potential biosynthesis, we have developed divergent total syntheses of
seven monoterpene indole alkaloids including mersicarpine, leuconodines B and D …
seven monoterpene indole alkaloids including mersicarpine, leuconodines B and D …
New strategies in the efficient total syntheses of polycyclic natural products
Conspectus Polycyclic natural products are an inexhaustible source of medicinal agents,
and their complex molecular architecture renders challenging synthetic targets where …
and their complex molecular architecture renders challenging synthetic targets where …
Harnessing the properties of natural products
A Boufridi, RJ Quinn - Annual review of pharmacology and …, 2018 - annualreviews.org
Natural products (NPs) have been used as traditional medicines since antiquity. With more
than 1060 estimated compounds with molecular weights less than 500 Da representing …
than 1060 estimated compounds with molecular weights less than 500 Da representing …
Enantioselective total syntheses of (+)-stemofoline and three congeners based on a biogenetic hypothesis
XZ Huang, LH Gao, PQ Huang - Nature Communications, 2020 - nature.com
The powerful insecticidal and multi-drug-resistance-reversing activities displayed by the
stemofoline group of alkaloids render them promising lead structures for further …
stemofoline group of alkaloids render them promising lead structures for further …
Divergent total syntheses of ITHQ-type bis-β-carboline alkaloids by regio-selective formal aza-[4+ 2] cycloaddition and late-stage C–H functionalization
Q Wang, F Guo, J Wang, X Lei - Chemical Science, 2023 - pubs.rsc.org
We herein report the first total syntheses of several bis-β-carboline alkaloids, picrasidines G,
S, R, and T, and natural product-like derivatives in a divergent manner. Picrasidines G, S …
S, R, and T, and natural product-like derivatives in a divergent manner. Picrasidines G, S …