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Synthesis and antifertility activity of zoapatanol analogs
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Incoming claims: where this work appears in other papers’ reference lists and arguments.
inferred← citeshttps://doi.org/10.1002/adsc.201901115openalex-snapshot
Electrochemical Difunctionalization of Olefines: Access to Selenomethyl‐Substituted Cyclic Ethers or Lactones
inferred← citeshttps://doi.org/10.1002/ange.19941062122openalex-snapshot
Totalsynthese von ( + )−2′S,3′R‐Zoapatanol
inferred← citeshttps://doi.org/10.1002/anie.199421821openalex-snapshot
A Total Synthesis of ( + )‐2′S, 3′R‐Zoapatanol
inferred← citeshttps://doi.org/10.1002/aoc.6555openalex-snapshot
Exciting progress in the transition metal‐catalyzed synthesis of oxepines, benzoxepines, dibenzoxepines, and other derivatives
inferred← citeshttps://doi.org/10.1002/chem.201003666openalex-snapshot
Total Synthesis of (+)‐(2′S,3′R)‐Zoapatanol Exploiting the B‐Alkyl Suzuki Reaction and the Nucleophilic Potential of the Sulfinyl Group
inferred← citeshttps://doi.org/10.1002/chin.198544217openalex-snapshot
ChemInform Abstract: SYNTHESIS AND ANTIFERTILITY ACTIVITY OF ZOAPATANOL ANALOGS
inferred← citeshttps://doi.org/10.1002/ejoc.201300267openalex-snapshot
Stereoselective Synthesis of Benzoxepines through Tandem Alkylation/Michael Addition to Vinylogous Carbonates
inferred← citeshttps://doi.org/10.1002/ejoc.202000850openalex-snapshot
Synthesis of Seven Membered Oxacycles: Recent Developments and New Approaches
inferred← citeshttps://doi.org/10.1002/ejoc.202500862openalex-snapshot
Cesium Carbonate‐Mediated Cascade Cyclization for the Efficient Synthesis of Fused Benzo[ b ]naphthooxepinone Derivatives
inferred← citeshttps://doi.org/10.1002/hlca.201200364openalex-snapshot
Synthesis of the Major Oxepane Segment of Zoapatanol
inferred← citeshttps://doi.org/10.1007/7081_2008_112openalex-snapshot
Heterocycles via Oxime Cycloadditions
inferred← citeshttps://doi.org/10.1007/s11030-022-10502-9openalex-snapshot
New oxacycles on the block: benzodioxepinones via a Passerini reaction
inferred← citeshttps://doi.org/10.1016/0022-4731(88)90004-0openalex-snapshot
A chemical classification of nonsteroidal antagonists of sex-steroid hormone action
inferred← citeshttps://doi.org/10.1016/0040-4039(88)85233-xopenalex-snapshot
A synthesis of zoapatanol
inferred← citeshttps://doi.org/10.1016/0957-4166(96)00149-8openalex-snapshot
Synthetic studies on zoapatanol: Construction of oxepanes via an intramolecular 1,3-dipolar cycloaddition strategy
inferred← citeshttps://doi.org/10.1016/j.bmc.2014.05.039openalex-snapshot
Polymer supported synthesis of a natural product-inspired oxepane library
inferred← citeshttps://doi.org/10.1016/j.gresc.2024.01.002openalex-snapshot
Controlled generation of ortho-quinone methides and (4+3) cyclization with 2-indolylalcohols by dual photoredox/Brønsted acid relay catalysis
inferred← citeshttps://doi.org/10.1016/j.tet.2011.10.023openalex-snapshot
Ring-closing metathesis and palladium-catalyzed formate reduction to 3-methyleneoxepanes. Formal synthesis of (−)-zoapatanol
inferred← citeshttps://doi.org/10.1016/j.tetasy.2003.10.006openalex-snapshot
Highly stereoselective synthesis of furano-oxepanes: intramolecular nitrone cycloaddition (INC) reactions on sugar derived 2-substituted allylic ethers
inferred← citeshttps://doi.org/10.1016/j.tetlet.2007.12.088openalex-snapshot
Synthetic studies toward zoapatanol
inferred← citeshttps://doi.org/10.1016/s0040-4020(01)89243-7openalex-snapshot
A Total Synthesis of (±)-Zoapatanol and Demethyl-ORF13811
inferred← citeshttps://doi.org/10.1016/s0040-4020(98)00596-1openalex-snapshot
Synthesis of seven-membered oxacycles
inferred← citeshttps://doi.org/10.1016/s0040-4039(00)88914-5openalex-snapshot
Intramolecular 1,3-dipolar additions in 4-O-allyl pyranoside 6-nitrones: An approach to chiral pyrano-pyrans and pyrano-oxepans
inferred← citeshttps://doi.org/10.1016/s0040-4039(01)00932-7openalex-snapshot
A convenient approach towards 2′-analogs of zoapatanol from d-glucose
inferred← citeshttps://doi.org/10.1016/s0065-7743(08)61127-6openalex-snapshot
Chapter 17. Chemical Control of Fertility
inferred← citeshttps://doi.org/10.1016/s1874-6004(08)80007-xopenalex-snapshot
Chapter 3 Total syntheses of zoapatanol
inferred← citeshttps://doi.org/10.1021/acs.joc.6c00465openalex-snapshot
Electrochemical Synthesis of 7-Membered Cyclic Ethers via Selenocyclization of Propargylic Benzyl Ethers
inferred← citeshttps://doi.org/10.1021/jo048115zopenalex-snapshot
Synthetic Approaches and Total Synthesis of Natural Zoapatanol
inferred← citeshttps://doi.org/10.1021/ol049008uopenalex-snapshot
Concise Asymmetric Synthesis of (5R)-6-Hydroxy-3,8-dioxabicyclo[3.2.1]octane Derivatives
inferred← citeshttps://doi.org/10.1021/ol049433nopenalex-snapshot
Total Synthesis of Natural (+)-(2‘S,3‘R)-Zoapatanol
inferred← citeshttps://doi.org/10.1039/c5ob02676hopenalex-snapshot
Gold( iii )-catalyzed synthesis of aroylbenzo[b]oxepin-3-ones from ortho-O-propargyl-1-one substituted arylaldehydes
inferred← citeshttps://doi.org/10.1055/s-0037-1611838openalex-snapshot
Concise Seven-Membered Oxepene/Oxepane Synthesis – Structural Motifs in Natural and Synthetic Products
inferred← citeshttps://doi.org/10.1073/pnas.1015269108openalex-snapshot
Biology-oriented synthesis of a natural-product inspired oxepane collection yields a small-molecule activator of the Wnt-pathway
inferred← citeshttps://doi.org/10.1080/00397918908052678openalex-snapshot
Regiospecific Synthesis of Dioxabicyclooctanes Containing a Terminal Prenyl Sidechain
inferred← citeshttps://doi.org/10.3987/com-13-12819openalex-snapshot
Synthesis of Dihydrooxepins by the Cycloaddition of 2-Amino-4,5-dihydro-3-furancarbonitriles with Dimethyl Acetylenedicarboxylate
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