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https://doi.org/10.2139/ssrn.4007110

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inferredcites →https://doi.org/10.1002/chir.20733openalex-extracted
ECD cotton effect approximated by the Gaussian curve and other methods
inferredcites →https://doi.org/10.1002/ejoc.201200725openalex-extracted
Nine 2‐(2‐Phenylethyl)chromone Derivatives from the Resinous Wood of Aquilaria sinensis and Their Inhibition of LPS‐Induced NO Production in RAW 264.7 Cells
inferredcites →https://doi.org/10.1002/hlca.201200069openalex-extracted
Eight New 2‐(2‐Phenylethyl)chromone (=2‐(2‐Phenylethyl)‐4 H ‐1‐benzopyran‐4‐one) Derivatives from Aquilaria malaccensis Agarwood
inferredcites →https://doi.org/10.1002/wcms.1327openalex-extracted
Software update: the ORCA program system, version 4.0
inferredcites →https://doi.org/10.1002/wcms.81openalex-extracted
The ORCA program system
inferredcites →https://doi.org/10.1007/s11418-018-1201-2openalex-extracted
Three new 5,6,7,8-tetrahydroxy-5,6,7,8-tetrahydrochromone derivatives enantiomeric to agarotetrol from agarwood
inferredcites →https://doi.org/10.1016/j.cclet.2008.05.034openalex-extracted
A new cytotoxic 2-(2-phenylethyl)chromone from Chinese eaglewood
inferredcites →https://doi.org/10.1016/j.fitote.2014.07.011openalex-extracted
2-(2-Phenylethyl)chromone derivatives from Chinese agarwood induced by artificial holing
inferredcites →https://doi.org/10.1016/j.fitote.2017.02.009openalex-extracted
Anti-inflammatory 2-(2-phenylethyl)chromone derivatives from Chinese agarwood
inferredcites →https://doi.org/10.1016/j.fitote.2019.04.007openalex-extracted
Four new guaiane sesquiterpenoids from agarwood of Aquilaria filaria
inferredcites →https://doi.org/10.1016/j.jscs.2013.09.002openalex-extracted
Synthesis and molecular modeling studies of novel pyrrole analogs as antimycobacterial agents
inferredcites →https://doi.org/10.1016/j.phytochem.2011.11.017openalex-extracted
2-(2-Phenylethyl)chromones from Chinese eaglewood
inferredcites →https://doi.org/10.1016/j.phytochem.2021.112920openalex-extracted
Eudesmane-type and agarospirane-type sesquiterpenes from agarwood of Aquilaria agallocha
inferredcites →https://doi.org/10.1016/j.phytol.2021.01.010openalex-extracted
Two new 2-(2-phenethyl)chromone derivatives from agarwood of Aquilaria walla and their cytotoxicity
inferredcites →https://doi.org/10.1017/s0020782900032319openalex-extracted
Convention on International Trade in Endangered Species of Wild Fauna and Flora (Cites) Compliance Procedures
inferredcites →https://doi.org/10.1039/d0np00042fopenalex-extracted
Natural products in agarwood and Aquilaria plants: chemistry, biological activities and biosynthesis
inferredcites →https://doi.org/10.1055/a-0645-1437openalex-extracted
Four New 2-(2-Phenylethyl)-4H-chromen-4-one Derivatives from the Resinous Wood of Aquilaria sinensis and Their Inhibitory Activities on Neutrophil Pro-Inflammatory Responses
inferredcites →https://doi.org/10.1080/10412905.1993.9698221openalex-extracted
Components of the Volatile Concentrate of Agarwood
inferredcites →https://doi.org/10.1248/cpb.37.1428openalex-extracted
The structure of AH16, new tetrahydroxy-2-(2-phenylethyl)chromone from agalwood.
inferredcites →https://doi.org/10.1248/cpb.50.419openalex-extracted
Six New 2-(2-Phenylethyl)chromones from Agarwood.
inferredcites →https://doi.org/10.1248/cpb.51.560openalex-extracted
Four New 2-(2-Phenylethyl)chromone Derivatives from Withered Wood of Aquilaria sinensis
inferredcites →https://doi.org/10.3389/fpls.2018.00712openalex-extracted
Genome Size, Molecular Phylogeny, and Evolutionary History of the Tribe Aquilarieae (Thymelaeaceae), the Natural Source of Agarwood
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