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Hispidanins A–D: Four New Asymmetric Dimeric Diterpenoids from the Rhizomes of Isodon hispida

https://doi.org/10.1021/ol501417k
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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/hlca.200490072openalex-snapshot
New ent‐Abietanoids from Isodon rubescens
inferredcites →https://doi.org/10.1002/hlca.200890249openalex-snapshot
Dimeric Diterpenes from the Roots of the Mangrove Plant Ceriops tagal
inferredcites →https://doi.org/10.1016/0031-9422(91)85030-4openalex-snapshot
Diterpenic adducts from Xylopia species
inferredcites →https://doi.org/10.1016/0031-9422(95)00417-3openalex-snapshot
Diterpenoids from leaves of Cryptomeria japonica
inferredcites →https://doi.org/10.1016/j.bse.2006.07.001openalex-snapshot
Diterpene adducts from branches of Xylopia emarginata
inferredcites →https://doi.org/10.1016/j.phytochem.2006.11.007openalex-snapshot
ent-Abietane diterpenoids from Isodon rubescens var. rubescens
inferredcites →https://doi.org/10.1016/j.tet.2007.09.039openalex-snapshot
Semisynthesis of labdane diterpene metabolites from the nudibranch Pleurobranchaea meckelii
inferredcites →https://doi.org/10.1016/s0968-0896(00)00096-1openalex-snapshot
The synthesis and antibacterial activity of totarol derivatives. part 3: modification of ring-B
inferredcites →https://doi.org/10.1039/b604174dopenalex-snapshot
Diterpenoids from Isodon species and their biological activities

What points at this work

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

inferred← citeshttps://doi.org/10.2139/ssrn.4135623openalex-extracted
Callicarpnoids A-C, Structurally Intriguing Ent -Clerodane Diterpenoid Dimers with Cytotoxicity Against MCF-7 And HCT-116 Cell Lines From Callicarpa Arborea
inferred← citeshttps://doi.org/10.1002/ange.201700838openalex-snapshot
Bioinspired Asymmetric Synthesis of Hispidanin A
inferred← citeshttps://doi.org/10.1002/ange.201700958openalex-snapshot
Asymmetric Total Synthesis of Hispidanin A
inferred← citeshttps://doi.org/10.1002/anie.201700838openalex-snapshot
Bioinspired Asymmetric Synthesis of Hispidanin A
inferred← citeshttps://doi.org/10.1002/anie.201700958openalex-snapshot
Asymmetric Total Synthesis of Hispidanin A
inferred← citeshttps://doi.org/10.1002/chem.201801156openalex-snapshot
Asymmetric Synthesis of Hispidanin A and Related Diterpenoids
inferred← citeshttps://doi.org/10.1002/ejoc.202400983openalex-snapshot
Recent Advances in Sustainable Total Synthesis and Chiral Pool Strategies with Emphasis on (−)‐Sclareol in Natural Products Synthesis
inferred← citeshttps://doi.org/10.1007/978-981-99-7329-3_14openalex-snapshot
Biological Activities
inferred← citeshttps://doi.org/10.1007/978-981-99-7329-3_3openalex-snapshot
Classification of Diverse Novel Diterpenoids
inferred← citeshttps://doi.org/10.1007/s11030-021-10195-6openalex-snapshot
Cross-coupling reactions towards the synthesis of natural products
inferred← citeshttps://doi.org/10.1016/j.bioorg.2022.106111openalex-snapshot
Callicarpnoids A–C, structurally intriguing ent-Clerodane diterpenoid dimers with cytotoxicity against MCF-7 and HCT-116 cell lines from Callicarpa arborea Roxb
inferred← citeshttps://doi.org/10.1016/j.jorganchem.2018.05.018openalex-snapshot
Recent applications of Stille reaction in total synthesis of natural products: An update
inferred← citeshttps://doi.org/10.1016/j.phytol.2021.10.017openalex-snapshot
Two new benzophenones from Dobinea delavayi
inferred← citeshttps://doi.org/10.1016/j.tet.2025.135074openalex-snapshot
Recent synthetic innovations in Stille coupling reaction: A review
inferred← citeshttps://doi.org/10.1021/acs.joc.1c00305openalex-snapshot
Fischdiabietane A, an Antitumoral Diterpenoid Dimer Featuring an Unprecedented Carbon Skeleton from Euphorbia fischeriana
inferred← citeshttps://doi.org/10.1021/acs.orglett.1c01724openalex-snapshot
Spiro ent-Clerodane Dimers: Discovery and Green Approaches for a Scalable Biomimetic Synthesis
inferred← citeshttps://doi.org/10.1039/c7np00027hopenalex-snapshot
Diterpenoids from Isodon species: an update
inferred← citeshttps://doi.org/10.1039/c7np00065kopenalex-snapshot
Total synthesis of complex terpenoids employing radical cascade processes
inferred← citeshttps://doi.org/10.1039/c8ob02082eopenalex-snapshot
Dimericursones A and B: two unprecedented hexacyclic dimeric diterpenoids from the root barks of Jatropha curcas
inferred← citeshttps://doi.org/10.1039/c9np00037bopenalex-snapshot
Naturally occurring [4 + 2] type terpenoid dimers: sources, bioactivities and total syntheses
inferred← citeshttps://doi.org/10.1039/c9np00062copenalex-snapshot
Natural disesquiterpenoids: an update
inferred← citeshttps://doi.org/10.1039/d1qo00999kopenalex-snapshot
Cunlanceloic acids A–D: unprecedented labdane diterpenoid dimers with AChE inhibitory and cytotoxic activities from Cunninghamia lanceolata
inferred← citeshttps://doi.org/10.1039/d2np00039copenalex-snapshot
Biogenetic and biomimetic synthesis of natural bisditerpenoids: hypothesis and practices
inferred← citeshttps://doi.org/10.1039/d3qo01679jopenalex-snapshot
Isoxerophilins A and B, two diterpene heterodimers from Isodon xerophilus : structural elucidation and semisynthesis of isoxerophilin analogues
inferred← citeshttps://doi.org/10.1039/d5cs00760gopenalex-snapshot
Radical retrosynthesis: a powerful strategy for modern assembly of terpenoid natural products
inferred← citeshttps://doi.org/10.1055/a-1532-4763openalex-snapshot
Recent Applications of the Diels–Alder Reaction in the Synthesis of Natural Products (2017–2020)
inferred← citeshttps://doi.org/10.1055/s-0036-1591935openalex-snapshot
Total Synthesis of Natural Terpenoids: Inspired but Not Limited by Biohypothesis
inferred← citeshttps://doi.org/10.1080/10286020.2018.1518321openalex-snapshot
New abietane diterpenoid glucosides from underground parts of Isodon taliensis
inferred← citeshttps://doi.org/10.1080/14786419.2020.1777410openalex-snapshot
Bioactive hydroxypropionylated glucose derivatives from Astragalus bhotanensis
inferred← citeshttps://doi.org/10.1080/14786419.2021.1994966openalex-snapshot
Four new phenolic glycosides from Dobinea delavayi
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