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The first total synthesis of 4-deoxyannomontacin

https://doi.org/10.1039/a900696f
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What this work says

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

inferredcites →https://doi.org/10.1016/s0304-3835(97)04716-2openalex-snapshot
The Annonaceous acetogenin bullatacin is cytotoxic against multidrug-resistant human mammary adenocarcinoma cells
inferredcites →https://doi.org/10.1021/ja00024a053openalex-snapshot
Synthesis of (+)-(15,16,19,20,23,24)-hexepi-uvaricin: a bis(tetrahydrofuranyl) annonaceous acetogenin analog
inferredcites →https://doi.org/10.1021/ja00253a032openalex-snapshot
Catalytic asymmetric epoxidation and kinetic resolution: modified procedures including in situ derivatization
inferredcites →https://doi.org/10.1021/ja01494a049openalex-snapshot
Some Oxidation and Reduction Products of 2,4-O-Ethylidene-D-erythrose1
inferredcites →https://doi.org/10.1021/jm9700169openalex-snapshot
Structure−Activity Relationships of Diverse Annonaceous Acetogenins against Multidrug Resistant Human Mammary Adenocarcinoma (MCF-7/Adr) Cells
inferredcites →https://doi.org/10.1021/jo00110a019openalex-snapshot
Synthetic Studies toward Mono-THF Annonaceous Acetogenins: A Diastereoselective and Convergent Approach to Corossolone and (10RS)-Corossoline
inferredcites →https://doi.org/10.1021/jo970423sopenalex-snapshot
Total Synthesis of the Annonaceous Acetogenin (+)-Asimicin. Development of a New Bidirectional Strategy
inferredcites →https://doi.org/10.1021/np50068a001openalex-snapshot
Annonaceous Acetogenins: A Review
inferredcites →https://doi.org/10.1039/np9961300275openalex-snapshot
Recent advances in annonaceous acetogenins
inferredcites →https://doi.org/10.3987/com-96-7562openalex-snapshot
Total Synthesis of (8'R)- and (8'S)-Corossoline

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.4176346openalex-extracted
Synthesis of Carbohydrate Analogues of the THF-Acetogenin 4-Deoxyannomontacin and Their Cytotoxicity Against Human Prostate Cancer Cell Lines
inferred← citeshttps://doi.org/10.1002/(sici)1520-636x(2000)12:3<127::aid-chir4>3.0.co;2-eopenalex-snapshot
Base-catalyzed epimerization of the butenolide in annonaceous acetogenins
inferred← citeshttps://doi.org/10.1002/1521-3765(20020402)8:7<1621::aid-chem1621>3.0.co;2-8openalex-snapshot
The Total Synthesis of the Annonaceous Acetogenin, Muricatetrocin C
inferred← citeshttps://doi.org/10.1002/ange.200462264openalex-snapshot
The Total Synthesis of the Annonaceous Acetogenin 10‐Hydroxyasimicin
inferred← citeshttps://doi.org/10.1002/anie.200462264openalex-snapshot
The Total Synthesis of the Annonaceous Acetogenin 10‐Hydroxyasimicin
inferred← citeshttps://doi.org/10.1002/chem.200390021openalex-snapshot
Studies on Mimicry of Naturally Occurring Annonaceous Acetogenins: Non‐THF Analogues Leading to Remarkable Selective Cytotoxicity against Human Tumor Cells
inferred← citeshttps://doi.org/10.1002/chin.199939202openalex-snapshot
ChemInform Abstract: The First Total Synthesis of 4‐Deoxyannomontacin.
inferred← citeshttps://doi.org/10.1002/ejoc.200500850openalex-snapshot
First Total Synthesis of Longimicin D
inferred← citeshttps://doi.org/10.1007/978-3-319-22692-7_2openalex-snapshot
Acetogenins from Annonaceae
inferred← citeshttps://doi.org/10.1016/j.carres.2022.108671openalex-snapshot
Synthesis of carbohydrate analogues of the THF-acetogenin 4-deoxyannomontacin and their cytotoxicity against human prostate cancer cell lines
inferred← citeshttps://doi.org/10.1016/j.tet.2007.05.047openalex-snapshot
Enantioselective syntheses of (−)-pinellic acid, α- and β-dimorphecolic acid
inferred← citeshttps://doi.org/10.1016/j.tet.2010.08.028openalex-snapshot
Synthesis of solamin type mono-THF acetogenins using cross-metathesis
inferred← citeshttps://doi.org/10.1016/j.tet.2011.04.072openalex-snapshot
Stereoselective total synthesis of (+)-sapinofuranone B
inferred← citeshttps://doi.org/10.1016/j.tetlet.2005.05.145openalex-snapshot
An iterative acetylene–epoxide coupling strategy for the total synthesis of longimicin C
inferred← citeshttps://doi.org/10.1016/j.tetlet.2007.01.163openalex-snapshot
Enantioselective synthesis of (−)-pinellic acid
inferred← citeshttps://doi.org/10.1021/jo048087kopenalex-snapshot
Efficient Total Synthesis of Sapinofuranone B
inferred← citeshttps://doi.org/10.1021/jo049084aopenalex-snapshot
Synthetic Studies Aimed at (−)-Cochleamycin A. Evaluation of Late-Stage Macrocyclization Alternatives
inferred← citeshttps://doi.org/10.1021/ol005504gopenalex-snapshot
The First Total Synthesis of Annonacin, the Most Typical Monotetrahydrofuran Annonaceous Acetogenins
inferred← citeshttps://doi.org/10.1021/ol0102592openalex-snapshot
Studies Aimed at the Total Synthesis of the Antitumor Antibiotic Cochleamycin A. An Enantioselective Biosynthesis-Based Pathway to the AB Bicyclic Core
inferred← citeshttps://doi.org/10.1021/ol302820copenalex-snapshot
Transannular O-Heterocyclization: A Useful Tool for the Total Synthesis of Murisolin and 16,19-cis-Murisolin
inferred← citeshttps://doi.org/10.1021/ol990062yopenalex-snapshot
The First Synthesis of Tonkinecin, an Annonaceous Acetogenin with a C-5 Carbinol Center
inferred← citeshttps://doi.org/10.1039/b609469bopenalex-snapshot
Recent progress on the total synthesis of natural products in China
inferred← citeshttps://doi.org/10.1039/c9nj05626bopenalex-snapshot
Synthesis of chiral propargyl alcohols following the base-induced elimination protocol: application in the total synthesis of natural products
inferred← citeshttps://doi.org/10.3418/jjam.23.26openalex-snapshot
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