Recent advances in the application of Diels–Alder reactions involving o-quinodimethanes, aza-o-quinone methides and o-quinone methides in natural product total …

B Yang, S Gao - Chemical Society Reviews, 2018 - pubs.rsc.org
In recent decades, transient and highly reactive ortho-quinodimethanes (o-QDMs), ortho-
quinone methides (o-QMs) and aza-ortho-quinone methides (aza-o-QMs) have attracted …

Novel natural products from extremophilic fungi

X Zhang, SJ Li, JJ Li, ZZ Liang, CQ Zhao - Marine Drugs, 2018 - mdpi.com
Extremophilic fungi have been found to develop unique defences to survive extremes of
pressure, temperature, salinity, desiccation, and pH, leading to the biosynthesis of novel …

A concise total synthesis of (−)‐Berkelic acid

HG Cheng, Z Yang, R Chen, L Cao… - Angewandte Chemie …, 2021 - Wiley Online Library
Reported here is a concise total synthesis of (−)‐berkelic acid in eight linear steps. This
synthesis features a Catellani reaction/oxa‐Michael cascade for the construction of the …

Benzannulated spiroketal natural products: isolation, biological activity, biosynthesis, and total synthesis

RM Gillard, MA Brimble - Organic & Biomolecular Chemistry, 2019 - pubs.rsc.org
The spiroketal moiety is an important privileged scaffold that occurs extensively in natural
products, drugs, and bioactive molecules. Naturally occurring spiroketals are numerous …

Diversity-Oriented Synthesis and Chemoinformatic Analysis of the Molecular Diversity of sp3-Rich Morpholine Peptidomimetics

E Lenci, R Innocenti, G Menchi, A Trabocchi - Frontiers in chemistry, 2018 - frontiersin.org
Diversity-Oriented Synthesis (DOS) consists of generating structurally diverse compounds
from a complexity-generating reaction followed by cyclization steps and appendage …

Application of palladium-catalyzed aryl C–H alkylation in total synthesis of (−)-berkelic acid

HH Wang, XD Wang, F Cao, WW Gao, SM Ma… - Organic Chemistry …, 2021 - pubs.rsc.org
An unprecedented palladium (II)-catalyzed ortho-alkylation of N-methoxybenzamide with
epoxides has been applied to the total synthesis of the isochroman natural product (–) …

Concise total synthesis of (−)-berkelic acid via regioselective spiroacetal/pyran formation

S Hanada, M Yoshida, H Kigoshi - Chemical Communications, 2024 - pubs.rsc.org
We successfully developed (1) scalable synthesis of the triol segment and (2) regio-and
stereoselective synthesis of the tetracyclic skeleton by tandem spiroacetal/pyran formation …

Gold (I)-mediated cycloisomerization/cycloaddition enables bioinspired syntheses of neonectrolides B–E and analogues

TJ Purgett, MW Dyer, B Bickel, J McNeely… - Journal of the …, 2019 - ACS Publications
Development of a synthetic route to the oxaphenalenone (OP) natural products
neonectrolides B–E is described. The synthesis relies on gold-catalyzed 6-endo-dig …

Eight-Step Asymmetric Synthesis of (–)-Berkelic Acid

Z Yang, HG Cheng, R Chen, L Cao, Q Wei, Q Wang… - …, 2022 - thieme-connect.com
We herein report an eight-step asymmetric synthesis of (–)-berkelic acid. This work features
a sequential Catellani-type reaction/oxa-Michael addition with epoxides as dual …

Horsfielenigans A and B, Two Rearranged Lignans with Anti‐Inflammatory Effects from Horsfieldia kingii

XH Zhang, Z Lu, ZY Li, N Fu, R Zhan - Chemistry & Biodiversity, 2023 - Wiley Online Library
Seven lignans were isolated from 70% aqueous acetone extracts of the twigs and leaves of
Horsfieldia kingii. Among these, new compounds 1–3 were identified by spectroscopic …