[HTML][HTML] Discovery and resupply of pharmacologically active plant-derived natural products: A review
AG Atanasov, B Waltenberger… - Biotechnology …, 2015 - Elsevier
Medicinal plants have historically proven their value as a source of molecules with
therapeutic potential, and nowadays still represent an important pool for the identification of …
therapeutic potential, and nowadays still represent an important pool for the identification of …
Divergent strategy in natural product total synthesis
L Li, Z Chen, X Zhang, Y Jia - Chemical reviews, 2018 - ACS Publications
The divergent total syntheses of complex natural products from a common intermediate have
attracted enormous attention in the chemical community in the past few years because it can …
attracted enormous attention in the chemical community in the past few years because it can …
Cross-coupling reactions using samarium (II) iodide
M Szostak, NJ Fazakerley, D Parmar… - Chemical …, 2014 - ACS Publications
Since its introduction to organic synthesis in 1977 by Kagan, 1, 2 samarium (II) iodide (SmI2,
Kagan's reagent) has gained the status of one of the most versatile single-electron transfer …
Kagan's reagent) has gained the status of one of the most versatile single-electron transfer …
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 …
Recent advances in the chemoselective reduction of functional groups mediated by samarium (II) iodide: a single electron transfer approach
M Szostak, M Spain, DJ Procter - Chemical Society Reviews, 2013 - pubs.rsc.org
Recently, samarium (II) iodide reductants have emerged as powerful single electron donors
for the highly chemoselective reduction of common functional groups. Complete control of …
for the highly chemoselective reduction of common functional groups. Complete control of …
Cutting-edge and time-honored strategies for stereoselective construction of C–N bonds in total synthesis
AK Mailyan, JA Eickhoff, AS Minakova, Z Gu… - Chemical …, 2016 - ACS Publications
The main objective of this review is to provide a comprehensive survey of methods used for
stereoselective construction of carbon–nitrogen bonds during the total synthesis of nitrogen …
stereoselective construction of carbon–nitrogen bonds during the total synthesis of nitrogen …
Total synthesis of (−)-daphnezomines A and B
G Xu, J Wu, L Li, Y Lu, C Li - Journal of the American Chemical …, 2020 - ACS Publications
Daphnezomines A and B are structurally unusual Daphniphyllum alkaloids that contain a
unique aza-adamantane core skeleton. Herein, a modular approach to these alkaloids is …
unique aza-adamantane core skeleton. Herein, a modular approach to these alkaloids is …
Asymmetric Construction of the Core of C6, C7-Epoxy Daphnane Diterpenoid Orthoesters
Y Sun, J Feng, S Qin, S Fu, B Liu - Organic Letters, 2023 - ACS Publications
Asymmetric construction of the core of C6, C7-epoxy daphnane diterpenoid orthoesters is
developed through a convergent synthetic strategy. The salient features include a …
developed through a convergent synthetic strategy. The salient features include a …
Samarium (ii) iodide-mediated reactions applied to natural product total synthesis
MM Heravi, A Nazari - RSC advances, 2022 - pubs.rsc.org
Natural product synthesis remains a field in which new synthetic methods and reagents are
continually being evaluated. Due to the demanding structures and complex functionality of …
continually being evaluated. Due to the demanding structures and complex functionality of …
Total Syntheses of Crinipellins Enabled by Cobalt‐Mediated and Palladium‐Catalyzed Intramolecular Pauson–Khand Reactions
Z Huang, J Huang, Y Qu, W Zhang, J Gong… - Angewandte …, 2018 - Wiley Online Library
Efficient total syntheses of the naturally occurring, potent antibiotic compounds (−)‐crinipellin
A and (−)‐crinipellin B are described. The key advanced intermediate, a fully functionalized …
A and (−)‐crinipellin B are described. The key advanced intermediate, a fully functionalized …