Navigating the chiral pool in the total synthesis of complex terpene natural products
ZG Brill, ML Condakes, CP Ting, TJ Maimone - Chemical reviews, 2017 - ACS Publications
The pool of abundant chiral terpene building blocks (ie,“chiral pool terpenes”) has long
served as a starting point for the chemical synthesis of complex natural products, including …
served as a starting point for the chemical synthesis of complex natural products, including …
Total synthesis of complex terpenoids employing radical cascade processes
K Hung, X Hu, TJ Maimone - Natural product reports, 2018 - pubs.rsc.org
Covering: 2011–2017 Radical cyclizations have a rich history in organic chemistry and have
been particularly generous to the field of natural product synthesis. Owing to their ability to …
been particularly generous to the field of natural product synthesis. Owing to their ability to …
Asymmetric total synthesis of illisimonin A
C Etling, G Tedesco, A Di Marco… - Journal of the American …, 2023 - ACS Publications
The discovery of illisimonin A in 2017 extended the structural repertoire of the Illicium
sesquiterpenoids─ a class of natural products known for their high oxidation levels and …
sesquiterpenoids─ a class of natural products known for their high oxidation levels and …
Applications of Knoevenagel condensation reaction in the total synthesis of natural products
The Knoevenagel condensation reaction is a prominent organic reaction commonly being
utilized in the total synthesis of natural and biologically potent products as a vital and …
utilized in the total synthesis of natural and biologically potent products as a vital and …
Trends in applying C–H oxidation to the total synthesis of natural products
Y Qiu, S Gao - Natural product reports, 2016 - pubs.rsc.org
Covering: 2006 to 2015 C–H functionalization remains one of the frontier challenges in
organic chemistry and drives quite an active area of research. It has recently been applied in …
organic chemistry and drives quite an active area of research. It has recently been applied in …
Making natural products from renewable feedstocks: back to the roots?
J Kühlborn, J Groß, T Opatz - Natural Product Reports, 2020 - pubs.rsc.org
Covering: up to mid-2019 This review highlights the utilization of biomass-derived building
blocks in the total synthesis of natural products. An overview over several renewable …
blocks in the total synthesis of natural products. An overview over several renewable …
Development of a Terpene Feedstock-Based Oxidative Synthetic Approach to the Illicium Sesquiterpenes
K Hung, ML Condakes, LFT Novaes… - Journal of the …, 2019 - ACS Publications
The Illicium sesquiterpenes are a family of natural products containing over 100 highly
oxidized and structurally complex members, many of which display interesting biological …
oxidized and structurally complex members, many of which display interesting biological …
Neurotrophic natural products: chemistry and biology
J Xu, MH Lacoske… - Angewandte Chemie …, 2014 - Wiley Online Library
Neurodegenerative diseases and spinal cord injury affect approximately 50 million people
worldwide, bringing the total healthcare cost to over 600 billion dollars per year. Nervous …
worldwide, bringing the total healthcare cost to over 600 billion dollars per year. Nervous …
An eight-step gram-scale synthesis of (−)-jiadifenolide
Abstract Development of a biologically active secondary metabolite into a useful medicine
requires continuous access to meaningful quantities of material. Although any chemical …
requires continuous access to meaningful quantities of material. Although any chemical …
An enantiospecific synthesis of jiadifenolide
DA Siler, JD Mighion… - Angewandte Chemie …, 2014 - Wiley Online Library
A Robinson annulation, van Leusen homologation, and a desymmetrizing C H oxidation
enabled an enantiospecific synthesis of the neurotrophic natural product jiadifenolide. From …
enabled an enantiospecific synthesis of the neurotrophic natural product jiadifenolide. From …