[HTML][HTML] Overview of the antimicrobial compounds produced by members of the Bacillus subtilis group

S Caulier, C Nannan, A Gillis, F Licciardi… - Frontiers in …, 2019 - frontiersin.org
Over the last seven decades, applications using members of the Bacillus subtilis group have
emerged in both food processes and crop protection industries. Their ability to form survival …

[HTML][HTML] The value of universally available raw NMR data for transparency, reproducibility, and integrity in natural product research

JB McAlpine, SN Chen, A Kutateladze… - Natural product …, 2019 - pubs.rsc.org
Covering: up to 2018 With contributions from the global natural product (NP) research
community, and continuing the Raw Data Initiative, this review collects a comprehensive …

Complex molecule synthesis by electrocatalytic decarboxylative cross-coupling

B Zhang, J He, Y Gao, L Levy, MS Oderinde… - Nature, 2023 - nature.com
Modern retrosynthetic analysis in organic chemistry is based on the principle of polar
relationships between functional groups to guide the design of synthetic routes. This …

Copper-catalyzed intramolecular alkene carboetherification: synthesis of fused-ring and bridged-ring tetrahydrofurans

Y Miller, L Miao, AS Hosseini… - Journal of the American …, 2012 - ACS Publications
Fused-ring and bridged-ring tetrahydrofuran scaffolds are found in a number of natural
products and biologically active compounds. A new copper-catalyzed intramolecular …

Enantioselective Copper‐Catalyzed Carboetherification of Unactivated Alkenes

MT Bovino, TW Liwosz, NE Kendel, Y Miller… - Angewandte …, 2014 - Wiley Online Library
Chiral saturated oxygen heterocycles are important components of bioactive compounds.
Cyclization of alcohols onto pendant alkenes is a direct route to their synthesis, but few …

[HTML][HTML] A visible light mediated, metal and oxidant free highly efficient cross dehydrogenative coupling (CDC) reaction between quinoxalin-2 (1 H)-ones and ethers

KD Mane, RB Kamble, G Suryavanshi - New Journal of Chemistry, 2019 - pubs.rsc.org
The efficient and metal free, white light mediated 3C alkylation of quinoxalin-2 (1H)-ones via
a cross dehydrogenative coupling reaction with cyclic ethers using eosin Y as a …

[HTML][HTML] Medicinal Chemistry of Annonaceous Acetogenins: Design, Synthesis, and Biological Evaluation of Novel Analogues

N Kojima, T Tanaka - Molecules, 2009 - mdpi.com
Most Annonaceous acetogenins are characterized by between one and three THF ring (s)
with one or two flanking hydroxyl group (s) in the center of a C32/34 fatty acid, and the …

Synthesis and tumor cell growth inhibitory activity of biotinylated annonaceous acetogenins

JF Shi, P Wu, ZH Jiang, XY Wei - European journal of medicinal chemistry, 2014 - Elsevier
Nineteen biotinylated squamocin/bullatacin derivatives have been synthesized for targeted
delivery to biotin receptor overexpressed tumor cells. Most biotinylated squamocin and …

Recent advances in the synthesis of tetrahydrofurans and applications in total synthesis

A de La Torre, C Cuyamendous, V Bultel-Poncé… - Tetrahedron, 2016 - Elsevier
Many natural products incorporate tetrahydrofuran (THF) moieties, including macrolides, 1
polyether ionophores, 2 acetogenins 3 or oxidized lipids, 4 with a wide array of bioactivities …

[HTML][HTML] The applications of catalytic asymmetric halocyclization in natural product synthesis

J Yan, Z Zhou, Q He, G Chen, H Wei… - Organic Chemistry …, 2022 - pubs.rsc.org
Halocyclization of olefinic substrate enables the establishment of cyclic skeletons via
intramolecular halonium-induced nucleophilic addition, which has been well utilized as a …