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[HTML][HTML] The chemistry of isoindole natural products
K Speck, T Magauer - Beilstein journal of organic chemistry, 2013 - beilstein-journals.org
This review highlights the chemical and biological aspects of natural products containing an
oxidized or reduced isoindole skeleton. This motif is found in its intact or modified form in …
oxidized or reduced isoindole skeleton. This motif is found in its intact or modified form in …
1-Isoindolinone scaffold-based natural products with a promising diverse bioactivity
Abstract Isoindolin-1-one or 1-isoindolinone framework is referred to phthalimidines or
benzo fused γ-lactams of the corresponding γ-amino carboxylic acids and has been of prime …
benzo fused γ-lactams of the corresponding γ-amino carboxylic acids and has been of prime …
Natural sesquiterpenoids
BM Fraga - Natural product reports, 2013 - pubs.rsc.org
Covering: 2012. Previous review: Nat. Prod. Rep. 2012, 29, 1334. This review covers the
isolation, structural determination, synthesis and chemical and microbiological …
isolation, structural determination, synthesis and chemical and microbiological …
Facile synthesis and first antifungal exploration of tetracyclic meroterpenoids:(+)-aureol,(−)-pelorol, and its analogs
S Sun, X He, J Yang, X Wang, S Li - Journal of Natural Products, 2024 - ACS Publications
As an important bioactive molecular backbone, drimane meroterpenoids have drawn a great
deal of attention from both pharmacologists and chemists. Inspired by the prevalidated …
deal of attention from both pharmacologists and chemists. Inspired by the prevalidated …
Cytotoxic compounds derived from marine sponges. A review (2010–2012)
This extensive review covers research published between 2010 and 2012 regarding new
compounds derived from marine sponges, including 62 species from 60 genera belonging …
compounds derived from marine sponges, including 62 species from 60 genera belonging …
Total Synthesis of Anti‐Cancer Meroterpenoids Dysideanone B and Dysiherbol A and Structural Reassignment of Dysiherbol A
C Chong, Q Zhang, J Ke, H Zhang, X Yang… - Angewandte …, 2021 - Wiley Online Library
The first total synthesis of marine anti‐cancer meroterpenoids dysideanone B and
dysiherbol A have been accomplished in a divergent way. The synthetic route features: 1) a …
dysiherbol A have been accomplished in a divergent way. The synthetic route features: 1) a …
Decarboxylative oxygenation via photoredox catalysis
The direct conversion of aliphatic carboxylic acids to their dehomologated carbonyl
analogues has been accomplished through photocatalytic decarboxylative oxygenation …
analogues has been accomplished through photocatalytic decarboxylative oxygenation …
[HTML][HTML] Bioactive prenyl-and terpenyl-quinones/hydroquinones of marine origin
The sea is a rich source of biological active compounds, among which terpenyl-quinones/
hydroquinones constitute a family of secondary metabolites with diverse pharmacological …
hydroquinones constitute a family of secondary metabolites with diverse pharmacological …
A modular synthesis of tetracyclic meroterpenoid antibiotics
R Wildermuth, K Speck, FL Haut, P Mayer… - Nature …, 2017 - nature.com
Stachyflin, aureol, smenoqualone, strongylin A, and cyclosmenospongine belong to a family
of tetracyclic meroterpenoids, which, by nature of their unique molecular structures and …
of tetracyclic meroterpenoids, which, by nature of their unique molecular structures and …
Stereoselective Synthesis of Xylodonin A and 22-Hydroxyxylodonin A and Discovery of Analogues with Cytotoxic Activity
YC Wu, GS Xu, HJ Li, YC Wu - Journal of Natural Products, 2024 - ACS Publications
The first and stereoselective synthesis of xylodonin A and 22-hydroxyxylodonin A, two
drimane-type sesquiterpenoid natural products, was developed from the readily available …
drimane-type sesquiterpenoid natural products, was developed from the readily available …