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Boneratamides A−C, New Sesquiterpenoids Isolated from the Marine Sponge Axinyssa a plysinoides
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What this work says
Outgoing claims: the papers this work cites, builds on, or argues with.
inferredcites →https://doi.org/10.1021/ja00493a054openalex-snapshot
Total synthesis of (-)-axisonitrile-3. An application of the reductive ring opening of vinylcyclopropanes
inferredcites →https://doi.org/10.1021/ja00493a055openalex-snapshot
Stereospecific total synthesis of gibberellic acid. A key tricyclic intermediate
inferredcites →https://doi.org/10.1021/ol035721sopenalex-snapshot
Ceratamines A and B, Antimitotic Heterocyclic Alkaloids Isolated from the Marine Sponge Pseudoceratina sp. Collected in Papua New Guinea
What points at this work
Incoming claims: where this work appears in other papers’ reference lists and arguments.
inferred← citeshttps://doi.org/10.11646/zootaxa.5298.1.1zenodo-depositor-declared
Two centuries of sponges (phylum Porifera) taxonomic studies in Indonesia (1820–2021): checklist and bibliography
inferred← citeshttps://doi.org/10.1002/9783527335855.marprod192openalex-snapshot
Porifera (Sponges)–2
inferred← citeshttps://doi.org/10.1002/9783527335855.marprod195openalex-snapshot
Porifera (Sponges)–5
inferred← citeshttps://doi.org/10.1002/cbdv.71504openalex-snapshot
Marine Natural Products From Indonesia and Their Biosynthetic Origins: Part 1: Terpenoids and Meroterpenoids
inferred← citeshttps://doi.org/10.1002/ejoc.201301206openalex-snapshot
A Biomimetic Approach to the Synthesis of the Core Structure of the Marine Sponge Terpene Halichonadin G
inferred← citeshttps://doi.org/10.1007/978-3-032-01098-8_2openalex-snapshot
Chemical Evolution of Indonesian Marine Natural Products
inferred← citeshttps://doi.org/10.1016/j.gresc.2024.08.004openalex-snapshot
Advances of Ugi reaction in natural product synthesis
inferred← citeshttps://doi.org/10.1016/j.tet.2006.08.070openalex-snapshot
Stereochemical challenges in characterizing nitrogenous spiro-axane sesquiterpenes from the Indo-Pacific sponges Amorphinopsis and Axinyssa
inferred← citeshttps://doi.org/10.1016/j.tet.2013.06.006openalex-snapshot
Total synthesis of penmacric acids via an intermolecular radical addition reaction
inferred← citeshttps://doi.org/10.1021/np800465nopenalex-snapshot
Sesquiterpenes from the Sponge Axinyssa isabela
inferred← citeshttps://doi.org/10.1039/c9ob02249jopenalex-snapshot
Total synthesis of exigurin: the Ugi reaction in a hypothetical biosynthesis of natural products
inferred← citeshttps://doi.org/10.1039/d0ra07501aopenalex-snapshot
Two decades of recent advances of Ugi reactions: synthetic and pharmaceutical applications
inferred← citeshttps://doi.org/10.1039/d2ob00486kopenalex-snapshot
Bioinspired total synthesis of boneratamides A–C
inferred← citeshttps://doi.org/10.1039/d3ob01837gopenalex-snapshot
Recent developments in the total synthesis of natural products using the Ugi multicomponent reactions as the key strategy
inferred← citeshttps://doi.org/10.3390/md17060364openalex-snapshot
Marine Natural Products from Indonesian Waters
inferred← citeshttps://doi.org/10.3987/com-16-13442openalex-snapshot
A Biomimetic Approach to the Synthesis of Terpene-Amino Acid Conjugates. The Ugi Reaction in the Hypothetical Biosynthesis of Marine Natural Products
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