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 …

Structure-activity relationships of sesquiterpene lactones

TJ Schmidt - Studies in natural products chemistry, 2006 - Elsevier
Sesquiterpene lactones (STLs) are one of the largest biogenetically homogenous groups of
natural products known. Currently, the Dictionary of Natural Products holds a total of over …

[HTML][HTML] Toxic activities of sesquiterpene lactones: structural and biochemical aspects

TJ Schmidt - Curr. Org. Chem, 1999 - books.google.com
As one of the largest groups of secondary plant metabolites, sesquiterpene lactones (STL)
possess a broad variety of conspicuous biological activities directed towards all types of …

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 …

[图书][B] The total synthesis of natural products

J ApSimon, DJ Goldsmith - 1973 - Wiley Online Library
Throughout the history of organic chemistry, we find that the study of natural products
frequently has provided the impetus for great advances. This is certainly true in total …

Preparation of α, β‐unsaturated carbonyl compounds and nitriles by selenoxide elimination

HJ Reich, S Wollowitz - Organic reactions, 2004 - Wiley Online Library
Hydrogenation and dehydrogenation reactions play a key role in synthetic organic
chemistry. The discoveries that selenium and sulfur substituents could be easily introduced …

Oxidative Entry into the Illicium Sesquiterpenes: Enantiospecific Synthesis of (+)-Pseudoanisatin

K Hung, ML Condakes, T Morikawa… - Journal of the American …, 2016 - ACS Publications
Illicium sesquiterpenes have been the subject of numerous synthetic efforts due to their
ornate and highly oxidized structures as well as significant biological activities. Herein we …

Total Syntheses of (−)-Majucin and (−)-Jiadifenoxolane A, Complex Majucin-Type Illicium Sesquiterpenes

ML Condakes, K Hung, SJ Harwood… - Journal of the …, 2017 - ACS Publications
We report the first chemical syntheses of both (−)-majucin and (−)-jiadifenoxolane A via 10
net oxidations from the ubiquitous terpene (+)-cedrol. Additionally, this approach allows for …

[HTML][HTML] Enantioselective total synthesis of (−)-jiadifenolide

J Xu, L Trzoss, WK Chang… - … Chemie (International ed …, 2011 - ncbi.nlm.nih.gov
The first total synthesis of jiadifenolide (1), a potent neurotrophic modulator, has been
reported. Highlights of the synthesis include: construction of the B ring via an asymmetric …

Naturally occurring β-lactones: Occurrence, syntheses and properties. A review

C Lowe, JC Vederas - Organic preparations and procedures …, 1995 - Taylor & Francis
A convulsant natural product known as anisatin was isolatedl over forty years ago from the
Japanese star anise Illicium anisatum, yet it was not until 1965 that it was characterized2 as …