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Racemic trinorsesquiterpenoids from the Beihai sponge Spongia officinalis : structure and biomimetic total synthesis

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What this work says

Outgoing claims: the papers this work cites, builds on, or argues with.

inferredcites →https://doi.org/10.1002/1099-0690(200105)2001:10<1873::aid-ejoc1873>3.0.co;2-oopenalex-snapshot

Total Synthesis of Korormicin

inferredcites →https://doi.org/10.1002/ejoc.201300084openalex-snapshot

Deuterium and Tritium Labelling of N‐Acyl‐ L ‐homoserine Lactones (AHLs) by Catalytic Reduction of a Double Bond in the Layer‐by‐Layer Method

inferredcites →https://doi.org/10.1002/hlca.201600077openalex-snapshot

New Highly Oxidized Formamidobisabolene‐Derived Sesquiterpenes from a Hainan Sponge Axinyssa variabilis

inferredcites →https://doi.org/10.1002/ptr.2650050202openalex-snapshot

Pharmacological studies on terpenoids from marine sponges: Analgesic and muscle relaxant effects

inferredcites →https://doi.org/10.1016/0040-4020(57)88037-5openalex-snapshot

The structure of dendrolasin

inferredcites →https://doi.org/10.1016/0040-4020(72)88131-6openalex-snapshot

Further linear furanoterpenes from marine sponges

inferredcites →https://doi.org/10.1016/0040-4020(84)85092-9openalex-snapshot

New antimicrobial diterpenes from the sponge spongia officinalis

inferredcites →https://doi.org/10.1016/j.apsb.2014.11.001openalex-snapshot

Chromopeptide A, a highly cytotoxic depsipeptide from the marine sediment-derived bacterium Chromobacterium sp. HS-13-94

inferredcites →https://doi.org/10.1016/j.bmcl.2010.10.138openalex-snapshot

Antiproliferative and apoptotic sesquiterpene lactones from Carpesium faberi

inferredcites →https://doi.org/10.1016/j.tet.2017.04.026openalex-snapshot

A facile method to enable a model phospholipid cell-permeable and photoactivatable

inferredcites →https://doi.org/10.1016/j.tet.2017.07.027openalex-snapshot

Axiriabilines A-D, uncommon nitrogenous eudesmane-type sesquiterpenes from the Hainan sponge Axinyssa variabilis

inferredcites →https://doi.org/10.1016/s0040-4020(01)00975-9openalex-snapshot

Stereoselective syntheses of syn 5-[1-hydroxy-2-(2-bromo-phenyl)-ethyl]-5-methyl-5H-furan-2-one and syn 5-[1-hydroxy-2-(2-methoxy-phenyl)-ethyl]-5-methyl-5H-furan-2-one

inferredcites →https://doi.org/10.1016/s0040-4020(01)97059-0openalex-snapshot

Isoagatholactone, a diterpene of a new structural type from the sponge Spongia officinalis

inferredcites →https://doi.org/10.1016/s0040-4020(01)98174-8openalex-snapshot

Furospongin-1, a new C-21 furanoterpene from the sponges Spongia officinalis and Hippospongia communis

inferredcites →https://doi.org/10.1016/s0040-4039(00)88369-0openalex-snapshot

New deterpenes from Spongia officinalis

inferredcites →https://doi.org/10.1016/s0040-4039(00)95630-2openalex-snapshot

Studies in polyether synthesis using polyepoxide cyclisations.

inferredcites →https://doi.org/10.1016/s0957-4166(02)00476-7openalex-snapshot

Lactones. Part 15: Synthesis of chiral spirolactones with a carane system—insect feeding deterrents

inferredcites →https://doi.org/10.1021/acs.jafc.6b05238openalex-snapshot

Structural and Stereochemical Studies of Laurokamurols A–C, Uncommon Bis-sesquiterpenoids from the Chinese Red Alga Laurencia okamurai Yamada

inferredcites →https://doi.org/10.1021/acs.orglett.7b01716openalex-snapshot

Xishacorenes A–C, Diterpenes with Bicyclo[3.3.1]nonane Nucleus from the Xisha Soft Coral Sinularia polydactyla

inferredcites →https://doi.org/10.1021/ja00011a006openalex-snapshot

High-field FT NMR application of Mosher's method. The absolute configurations of marine terpenoids

inferredcites →https://doi.org/10.1021/ja00481a044openalex-snapshot

Acetylenic bond participation in biomimetic polyene cyclizations. Model studies directed toward the synthesis of 20-keto steroids. Synthesis of dl-progesterone and dl-.DELTA.4-androstene-3,17-dione

inferredcites →https://doi.org/10.1021/jo050336xopenalex-snapshot

Microwave-Mediated Claisen Rearrangement Followed by Phenol Oxidation: A Simple Route to Naturally Occurring 1,4-Benzoquinones. The First Syntheses of Verapliquinones A and B and Panicein A

inferredcites →https://doi.org/10.1021/np0400961openalex-snapshot

Isocyanide Terpene Metabolites of Phyllidiella pustulosa, a Nudibranch from the South China Sea

inferredcites →https://doi.org/10.1021/np200226uopenalex-snapshot

Bioactive Terpenes from Spongia officinalis

inferredcites →https://doi.org/10.1021/np50066a010openalex-snapshot

Terpenoids from the North Adriatic Sponge Spongia officinalis

inferredcites →https://doi.org/10.1021/np970160xopenalex-snapshot

New Furanoterpenoids from the Sponge Spongia officinalis

inferredcites →https://doi.org/10.1039/b604586copenalex-snapshot

Heterocyclic terpenes: linear furano- and pyrroloterpenoids

inferredcites →https://doi.org/10.1099/mic.0.26280-0openalex-snapshot

Mutation of lasA and lasB reduces Pseudomonas aeruginosa invasion of epithelial cells

inferredcites →https://doi.org/10.1111/j.1365-2958.1991.tb00822.xopenalex-snapshot

Pseudomonas aeruginosa LasA: a second elastase under the transcriptional control of lasR

inferredcites →https://doi.org/10.4155/fmc.15.169openalex-snapshot

Bioactive Isoquinolinequinone Alkaloids from the South China Sea Nudibranch Jorunna Funebris and Its Sponge-Prey Xestospongia Sp.

What points at this work

Incoming claims: where this work appears in other papers’ reference lists and arguments.

inferred← citeshttps://doi.org/10.1016/j.phytochem.2021.113006zenodo-depositor-declared

Jellynolide A, pokepola esters, and sponalisolides from the aquaculture sponge Spongia officinalis L

inferred← citeshttps://doi.org/10.1002/cbdv.202400519openalex-snapshot

Anti‐inflammatory Steroids from the South China Sea Sponge Spongia officinalis

inferred← citeshttps://doi.org/10.1002/cmdc.202500904openalex-snapshot

Synthesis of Benzopyrans and Quinolines with Nitrogenated Chain and Their Cytotoxicity Against Human Cancer Cell Lines

inferred← citeshttps://doi.org/10.1016/b978-0-443-31482-7.00122-3openalex-snapshot

One or More =CH, =CC, and/or C=C Bond(s) Formed by Rearrangement

inferred← citeshttps://doi.org/10.1016/j.bioorg.2021.104887openalex-snapshot

Diversity-oriented synthesis of cembranoid derivatives as potential anti-inflammatory agents

inferred← citeshttps://doi.org/10.1016/j.bmc.2021.116532openalex-snapshot

Synthesis and biological studies of “Polycerasoidol” and “trans-δ-Tocotrienolic acid” derivatives as PPARα and/or PPARγ agonists

inferred← citeshttps://doi.org/10.1016/j.tet.2021.132204openalex-snapshot

Polyoxygenated cembranoids from the Hainan soft coral Lobophytum crassum

inferred← citeshttps://doi.org/10.1016/j.tet.2023.133388openalex-snapshot

Scalarane sesterterpenes from the South China Sea sponge Hyrtios erecta and their PTP1B inhibitory activity

inferred← citeshttps://doi.org/10.1021/acs.jnatprod.9b00270openalex-snapshot

Spongian Diterpenes Including One with a Rearranged Skeleton from the Marine Sponge Spongia officinalis

inferred← citeshttps://doi.org/10.1021/acs.joc.4c02689openalex-snapshot

Uncommon Diterpenoids with Diverse Frameworks from the South China Sea Sponge Spongia officinalis and Their Anti-inflammatory Activities

inferred← citeshttps://doi.org/10.1021/acs.joc.9b00030openalex-snapshot

Rare Cembranoids from Chinese Soft Coral Sarcophyton ehrenbergi: Structural and Stereochemical Studies

inferred← citeshttps://doi.org/10.1021/jacs.2c13289openalex-snapshot

Catalytic Cross-Metathesis Reactions That Afford E- and Z-Trisubstituted Alkenyl Bromides: Scope, Applications, and Mechanistic Insights

inferred← citeshttps://doi.org/10.1021/jacs.5c15956openalex-snapshot

Enantioselective Trifunctionalization of Terminal Alkynes

inferred← citeshttps://doi.org/10.1021/jacs.6c09135openalex-snapshot

Piecewise Stereoselective Assembly of Multisubstituted Alkenes

inferred← citeshttps://doi.org/10.1038/s41401-022-00980-wopenalex-snapshot

Chemistry and bioactivity of secondary metabolites from South China Sea marine fauna and flora: recent research advances and perspective

inferred← citeshttps://doi.org/10.1080/14786419.2018.1561683openalex-snapshot

A new 5α,8α-epidioxysterol with immunosuppressive activity from the South China Sea soft coral Sinularia sp.

inferred← citeshttps://doi.org/10.1080/14786419.2021.1961137openalex-snapshot

Two new spongian diterpene derivatives from the aquaculture sponge Spongia officinalis Linnaeus, 1759

inferred← citeshttps://doi.org/10.3390/md19010038openalex-snapshot

An Anti-Inflammatory 2,4-Cyclized-3,4-Secospongian Diterpenoid and Furanoterpene-Related Metabolites of a Marine Sponge Spongia sp. from the Red Sea

inferred← citeshttps://doi.org/10.3390/md22050213openalex-snapshot

Spongia Sponges: Unabated Sources of Novel Secondary Metabolites

inferred← citeshttps://doi.org/10.3390/md23030096openalex-snapshot

Bioactive Terpenes from Marine Sponges and Their Associated Organisms

inferred← citeshttps://doi.org/10.3390/molecules27041279openalex-snapshot

Natural Enantiomers: Occurrence, Biogenesis and Biological Properties

inferred← citeshttps://doi.org/10.3390/molecules30163370openalex-snapshot

Trisubstituted Alkenes as Valuable Building Blocks

inferred← citeshttps://doi.org/10.3390/plants11060769openalex-snapshot

Structures, Occurrences and Biosynthesis of 11,12,13-Tri-nor-Sesquiterpenes, an Intriguing Class of Bioactive Metabolites

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