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Highly Selective Synthesis of Z -Unsaturated Esters by Using New Horner−Emmons Reagents, Ethyl (Diarylphosphono)acetates

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What this work says

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

inferredcites →https://doi.org/10.1016/0040-4039(95)00726-sopenalex-snapshot
Practical synthesis of Z-unsaturated esters by using a new Horner-Emmons reagent, ethyl diphenylphosphonoacetate
inferredcites →https://doi.org/10.1016/s0040-4020(01)93261-2openalex-snapshot
Further synthetic studies on rifamycin s
inferredcites →https://doi.org/10.1016/s0040-4039(00)79655-9openalex-snapshot
1,3-dimethyl 2-oxo 1,3,2-diazaphospholidine precursor of (Z) α,β-unsaturated esters.
inferredcites →https://doi.org/10.1016/s0040-4039(00)85909-2openalex-snapshot
Direct synthesis of Z-unsaturated esters. A useful modification of the horner-emmons olefination.
inferredcites →https://doi.org/10.1021/cr00094a007openalex-snapshot
The Wittig olefination reaction and modifications involving phosphoryl-stabilized carbanions. Stereochemistry, mechanism, and selected synthetic aspects
inferredcites →https://doi.org/10.1021/ja00046a009openalex-snapshot
A novel 1,8-photoaddition of dimethyl 1,4-naphthalenedicarboxylate to alkenes
inferredcites →https://doi.org/10.1021/ja00202a067openalex-snapshot
A triply convergent enantioselective total synthesis of (+)-ikarugamycin
inferredcites →https://doi.org/10.1021/jo00297a077openalex-snapshot
Palladium(0)-catalyzed reaction of (Z)-2-butene-1,4-diyl bis(methyl carbonate) and (Z)-2-butene-1,4-diyl diacetate with bifunctional nitrogen nucleophiles
inferredcites →https://doi.org/10.1021/jo01014a005openalex-snapshot
The Stereochemistry of the Phosphonate Modification of the Wittig Reaction
inferredcites →https://doi.org/10.1080/00397919008052333openalex-snapshot
Modified Wittig Reactions Using Triethylamine and Lithium Halides: Synthesis of α,β-Unsaturated Esters from Ketones and Ethyl Bis(Trifluoroethyl)Phosphonoacetate

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.2020.112287zenodo-depositor-declared
Essential structural features of (2Z,4E)-5-phenylpenta-2,4-dienoic acid for inhibition of root gravitropism
inferred← citeshttps://doi.org/10.2139/ssrn.4161448openalex-extracted
inferred← citeshttps://doi.org/10.1002/047084289x.rn01590openalex-snapshot
Ethyl 2-(diphenoxyphosphinyl) acetate
inferred← citeshttps://doi.org/10.1002/0471264180.or072.02openalex-snapshot
Desulfonylation Reactions
inferred← citeshttps://doi.org/10.1002/0471264229.os088.14openalex-snapshot
Preparation of Horner‐Wadsworth‐Emmons Reagent: Methyl 2‐Benzyloxycarbonylamino‐2‐(Dimethoxy‐ Phosphinyl)Acetate
inferred← citeshttps://doi.org/10.1002/1521-3757(20000804)112:15<2866::aid-ange2866>3.0.co;2-6openalex-snapshot
Vollständige Stereoselektivität bei der durch Samarium(II)-iodid vermittelten Synthese von (E)-α,β-ungesättigten Estern und Amiden
inferred← citeshttps://doi.org/10.1002/9780470638859.conrr332openalex-snapshot
Horner‐Wadsworth‐Emmons Olefination
inferred← citeshttps://doi.org/10.1002/9780471264194.fos05075openalex-snapshot
Ethyl (diarylphosphono)acetate
inferred← citeshttps://doi.org/10.1002/9781118354520.ch15openalex-snapshot
Catalytic Variants of Phosphine Oxide‐Mediated Organic Transformations
inferred← citeshttps://doi.org/10.1002/9781118662083.cot02-004openalex-snapshot
Formation of Alkenes by Wittig and Related Reactions
inferred← citeshttps://doi.org/10.1002/9781118754085.ch3openalex-snapshot
Fatty Acids and their Derivatives
inferred← citeshttps://doi.org/10.1002/9783527628087.ch1openalex-snapshot
Stilbenes Preparation and Analysis
inferred← citeshttps://doi.org/10.1002/9783527809080.cataz00883openalex-snapshot
Ando ester condensation
inferred← citeshttps://doi.org/10.1002/adsc.200404338openalex-snapshot
Efficient and Scalable Protocol for the Z‐Selective Synthesis of Unsaturated Esters by HornerWadsworthEmmons Olefination
inferred← citeshttps://doi.org/10.1002/ange.200460434openalex-snapshot
Stereoselective Total Synthesis of the Ionophore Antibiotic Zincophorin
inferred← citeshttps://doi.org/10.1002/ange.201201369openalex-snapshot
Enantioselective Total Synthesis of Marine Diterpenoid Clavulactone
inferred← citeshttps://doi.org/10.1002/ange.201506366openalex-snapshot
Totalsynthese von (+)‐Rubriflordilacton A
inferred← citeshttps://doi.org/10.1002/ange.201600055openalex-snapshot
The Total Synthesis of (±)‐Naupliolide: A Tetracyclic Sesquiterpene Lactone
inferred← citeshttps://doi.org/10.1002/ange.201610636openalex-snapshot
An Expedient Total Synthesis of Chivosazole F: an Actin‐Binding Antimitotic Macrolide from the Myxobacterium Sorangium Cellulosum
inferred← citeshttps://doi.org/10.1002/ange.201811403openalex-snapshot
Asymmetric Total Synthesis of Brasilicardins
inferred← citeshttps://doi.org/10.1002/ange.202316259openalex-snapshot
Bent π‐Conjugation within a Macrocycle: Asymmetric Total Syntheses of Spirohexenolides A and B
inferred← citeshttps://doi.org/10.1002/anie.200460434openalex-snapshot
Stereoselective Total Synthesis of the Ionophore Antibiotic Zincophorin
inferred← citeshttps://doi.org/10.1002/anie.201201369openalex-snapshot
Enantioselective Total Synthesis of Marine Diterpenoid Clavulactone
inferred← citeshttps://doi.org/10.1002/anie.201506366openalex-snapshot
Total Synthesis of (+)‐Rubriflordilactone A
inferred← citeshttps://doi.org/10.1002/anie.201600055openalex-snapshot
The Total Synthesis of (±)‐Naupliolide: A Tetracyclic Sesquiterpene Lactone
inferred← citeshttps://doi.org/10.1002/anie.201610636openalex-snapshot
An Expedient Total Synthesis of Chivosazole F: an Actin‐Binding Antimitotic Macrolide from the Myxobacterium Sorangium Cellulosum
inferred← citeshttps://doi.org/10.1002/anie.201811403openalex-snapshot
Asymmetric Total Synthesis of Brasilicardins
inferred← citeshttps://doi.org/10.1002/anie.202316259openalex-snapshot
Bent π‐Conjugation within a Macrocycle: Asymmetric Total Syntheses of Spirohexenolides A and B
inferred← citeshttps://doi.org/10.1002/asia.202200650openalex-snapshot
Reductive SN2’ Reaction of Epoxydienoate with Borane and its Application to the Synthesis and Structural Revision of an Antitumor Active Torrubiellutin Analogue
inferred← citeshttps://doi.org/10.1002/cbdv.201400391openalex-snapshot
Detection of a New Piperideine Alkaloid in the Pygidial Glands of Some Stenus Beetles
inferred← citeshttps://doi.org/10.1002/cctc.202001139openalex-snapshot
A Ring Closing Metathesis Approach to the Formal Synthesis of (+)‐Callyspongiolide
inferred← citeshttps://doi.org/10.1002/chem.200305709openalex-snapshot
Strategy for Enantio‐ and Diastereoselective Syntheses of All Possible Stereoisomers of 1,3‐Polyol Arrays Based on a Highly Catalyst‐Controlled Epoxidation of α,β‐Unsaturated Morpholinyl Amides: Application to Natural Product Synthesis
inferred← citeshttps://doi.org/10.1002/chem.200903500openalex-snapshot
Total Synthesis and Configurational Assignment of Chondramide A
inferred← citeshttps://doi.org/10.1002/chem.201000104openalex-snapshot
Good Timing in Total Synthesis: The Case of Phoslactomycin A
inferred← citeshttps://doi.org/10.1002/chem.201201585openalex-snapshot
The Plakotenins: Biomimetic Diels–Alder Reactions, Total Synthesis, Structural Investigations, and Chemical Biology
inferred← citeshttps://doi.org/10.1002/chem.201605287openalex-snapshot
Total Synthesis of Mycobacterium tuberculosis Dideoxymycobactin‐838 and Stereoisomers: Diverse CD1a‐Restricted T Cells Display a Common Hierarchy of Lipopeptide Recognition
inferred← citeshttps://doi.org/10.1002/chem.201703229openalex-snapshot
Total Synthesis of the Schisandraceae Nortriterpenoid Rubriflordilactone A
inferred← citeshttps://doi.org/10.1002/chem.202303626openalex-snapshot
Photo‐Catalyzed Acyl Azolium Promoted Selective α‐C(sp3)−H Acylation of Acetone via HAT: Access to Thermodynamically Less Favoured (Z)‐α,β‐Unsaturated Ketones
inferred← citeshttps://doi.org/10.1002/chin.199733080openalex-snapshot
ChemInform Abstract: Highly Selective Synthesis of Z‐Unsaturated Esters by Using New Horner‐ Emmons Reagents, Ethyl (Diarylphosphono)acetates.
inferred← citeshttps://doi.org/10.1002/chin.200815249openalex-snapshot
ChemInform Abstract: Total Synthesis of Marine Macrolides
inferred← citeshttps://doi.org/10.1002/cjoc.200890197openalex-snapshot
Asymmetric Total Synthesis of (−)‐Cladospolide B
inferred← citeshttps://doi.org/10.1002/cjoc.201190015openalex-snapshot
Synthesis of Stereoisomers of Cryptofolione 6′‐Mono‐ and 4′,6′‐Di‐O‐benzyl Ethers
inferred← citeshttps://doi.org/10.1002/cmdc.200700101openalex-snapshot
Cis‐Configured Aziridines Are New Pseudo‐Irreversible Dual‐Mode Inhibitors of Candida albicans Secreted Aspartic Protease 2
inferred← citeshttps://doi.org/10.1002/cmdc.201700084openalex-snapshot
Synthesis and Cytotoxicity Evaluation of C4‐ and C5‐Modified Analogues of the α,β‐Unsaturated Lactone of Pironetin
inferred← citeshttps://doi.org/10.1002/ejoc.200400005openalex-snapshot
9‐Demethyl‐9‐haloretinals by Wadsworth−Emmons Coupling − Easy Preparation of Pure (all‐E), (9Z) and (11Z) Isomers
inferred← citeshttps://doi.org/10.1002/ejoc.200400769openalex-snapshot
Phosphonate Modification for a Highly (Z)‐Selective Synthesis of Unsaturated Esters by Horner–Wadsworth–Emmons Olefination
inferred← citeshttps://doi.org/10.1002/ejoc.200500963openalex-snapshot
Asymmetric Dihydroxylation of β,γ‐Unsaturated Carboxylic Esterswith Trisubstituted C=C Bonds – Enantioselective Syntheses of Trisubstituted γ‐Butyrolactones
inferred← citeshttps://doi.org/10.1002/ejoc.200801234openalex-snapshot
Synthesis of the C11–C23 Fragment of the Potent Antitumor Agent Dictyostatin
inferred← citeshttps://doi.org/10.1002/ejoc.200900176openalex-snapshot
Stereoselective Synthesis of (2E,4Z)‐Dienamides Employing (Triphenylphosphoranylidene)ketene
inferred← citeshttps://doi.org/10.1002/ejoc.201000781openalex-snapshot
Isolation and Synthesis of Chivotriene, a Chivosazole Shunt Product from Sorangium cellulosum
inferred← citeshttps://doi.org/10.1002/ejoc.201001097openalex-snapshot
Synthesis of the Macrolactone of Migrastatin and Analogues with Potent Cell‐Migration Inhibitory Activity
inferred← citeshttps://doi.org/10.1002/ejoc.201100510openalex-snapshot
Stereoselective Total Synthesis of Umuravumbolide
inferred← citeshttps://doi.org/10.1002/ejoc.201100886openalex-snapshot
Stereoselective Synthesis of Aza Analogues of Isoaltholactone and Goniothalesdiol – New Applications of the Heck–Matsuda Reaction
inferred← citeshttps://doi.org/10.1002/ejoc.201100888openalex-snapshot
Stereoselective Total Synthesis of Polyrhacitides A and B
inferred← citeshttps://doi.org/10.1002/ejoc.201300112openalex-snapshot
Stereoselective Synthesis of (E)‐α,β‐Dehydroamino Acid Esters
inferred← citeshttps://doi.org/10.1002/ejoc.201300182openalex-snapshot
Stereocontrolled Synthesis of a Cn–Cn+6Building Block for the Unnatural Enantiomers of Important Polyol,Polyene Antibiotics from an Epoxy Alcohol by a Reduction/Conjugate Addition/Hydroxylation Sequence
inferred← citeshttps://doi.org/10.1002/ejoc.201300302openalex-snapshot
Total Synthesis of Umuravumbolide and Hyptolide Through Silicon‐Tethered Ring‐Closing Metathesis
inferred← citeshttps://doi.org/10.1002/ejoc.201402675openalex-snapshot
An Efficient Partial Reduction of α,β‐Unsaturated Esters Using DIBAL‐H in Flow
inferred← citeshttps://doi.org/10.1002/ejoc.201402720openalex-snapshot
Flexible Synthesis of Planar Chiral Azoninones and Optically Active Indolizidinones
inferred← citeshttps://doi.org/10.1002/ejoc.201500629openalex-snapshot
Synthesis of the C‐8–C‐24 Fragment of Maltepolide C by Using a Tandem Dihydroxylation/SN2 Cyclization Sequence
inferred← citeshttps://doi.org/10.1002/ejoc.201501370openalex-snapshot
Spiroketal Formation by Cascade Oxidative Dearomatization: An Approach to the Phorbaketal Skeleton
inferred← citeshttps://doi.org/10.1002/ejoc.202200222openalex-snapshot
Total Synthesis of 12,13‐Dibenzyl‐banistenoside B and Analogs
inferred← citeshttps://doi.org/10.1002/ejoc.202200365openalex-snapshot
Z‐Selective Alkene Formation from Reductive Aldehyde Homo‐Couplings
inferred← citeshttps://doi.org/10.1002/hc.10004openalex-snapshot
“One‐pot” synthesis of (Z)‐2‐aryl‐1‐(2‐cyanoethyl)ethenylphosphonates via hexamethylphosphoramide‐promoted sequential transformation
inferred← citeshttps://doi.org/10.1002/hc.10142openalex-snapshot
A convenient synthesis of substituted 3‐alkoxycarbonyl‐β,γ‐unsaturated esters with predominant Z‐selectivity
inferred← citeshttps://doi.org/10.1002/hc.20054openalex-snapshot
Synthesis of β‐monosubstituted α,β‐unsaturated amides with Z‐selectivity using diphenylphosphonoacetamides
inferred← citeshttps://doi.org/10.1002/jccs.200400193openalex-snapshot
Enantioselective Synthesis of Several Natural Virologins
inferred← citeshttps://doi.org/10.1002/jccs.201200466openalex-snapshot
Ti(Oi‐Pr)4 Mediated Olefination between Julia Reagent and Aldehydes under Mild Conditions: Facile Synthesis of Vinyl Sulfones
inferred← citeshttps://doi.org/10.1002/tcr.202200159openalex-snapshot
Diarylprolinol as an Effective Organocatalyst in Asymmetric Cross‐Aldol Reactions of Two Different Aldehydes
inferred← citeshttps://doi.org/10.1007/128_2012_314openalex-snapshot
Olefination Reactions of Phosphorus-Stabilized Carbon Nucleophiles
inferred← citeshttps://doi.org/10.1007/3-540-30031-7_135openalex-snapshot
Horner-Wadsworth-Emmons reaction
inferred← citeshttps://doi.org/10.1007/3-540-46100-0_6openalex-snapshot
Phosphonate Chemistry and Reagents in the Synthesis of Biologically Active and Natural Products
inferred← citeshttps://doi.org/10.1007/7081_016openalex-snapshot
Total Synthesis of Marine Macrolides
inferred← citeshttps://doi.org/10.1007/978-3-319-03979-4_138openalex-snapshot
Horner–Wadsworth–Emmons reaction
inferred← citeshttps://doi.org/10.1007/978-3-662-04835-1_138openalex-snapshot
Horner—Wadsworth—Emmons reaction
inferred← citeshttps://doi.org/10.1007/978-3-662-05336-2_148openalex-snapshot
Horner-Wadsworth-Emmons reaction
inferred← citeshttps://doi.org/10.1007/978-3-662-65244-2_3openalex-snapshot
Aufbau und Derivatisierung von CC-Mehrfachbindungen
inferred← citeshttps://doi.org/10.1007/978-3-662-70963-4_3openalex-snapshot
Synthesis and Derivatization of Alkenes and Alkynes
inferred← citeshttps://doi.org/10.1007/978-981-97-1619-7_1openalex-snapshot
A Journey to the Total Synthesis of Brasilicardins
inferred← citeshttps://doi.org/10.1007/bf02969265openalex-snapshot
A convenient synthesis of an anti-helicobacter pylori agent, dehydrodiconiferyl alcohol
inferred← citeshttps://doi.org/10.1007/s11172-006-0017-5openalex-snapshot
Phosphorylated methano[60]fullerenes containing nitroxyl radicals: synthesis, structures, and electrochemical behavior
inferred← citeshttps://doi.org/10.1007/s41207-024-00596-yopenalex-snapshot
New polysaccharide-based bio-super-absorbents for water stress control in agriculture: preparation and properties
inferred← citeshttps://doi.org/10.1016/b0-08-044655-8/00016-7openalex-snapshot
One or More CC Bond(s) Formed by Condensation: Condensation of P, As, Sb, Bi, Si, Ge, B, or Metal Functions
inferred← citeshttps://doi.org/10.1016/b978-0-08-097742-3.00120-8openalex-snapshot
1.15 Olefination of Carbonyl Compounds by Main-Group Element Mediators
inferred← citeshttps://doi.org/10.1016/b978-0-323-96025-0.00082-xopenalex-snapshot
Wittig and Horner-Wadsworth-Emmons Reactions
inferred← citeshttps://doi.org/10.1016/b978-0-443-31482-7.00059-xopenalex-snapshot
One or More C=C Bond(s) Formed by Condensation: Condensation of P, As, Sb, Bi, Si, B, Ge, Te or Metal Functions
inferred← citeshttps://doi.org/10.1016/b978-012526451-8/50005-9openalex-snapshot
Total Synthesis of Macrolides
inferred← citeshttps://doi.org/10.1016/j.arabjc.2016.01.008openalex-snapshot
Modular total syntheses of thymifodioic/incanic acids
inferred← citeshttps://doi.org/10.1016/j.aspen.2017.09.003openalex-snapshot
Attractiveness of male azuki bean beetle to the synthetic blends of 2E- and 2Z-homofarnesals
inferred← citeshttps://doi.org/10.1016/j.bioorg.2022.105915openalex-snapshot
Cytotoxicity of phenylpironetin analogs and the metabolic fate of pironetin and phenylpironetin
inferred← citeshttps://doi.org/10.1016/j.bmc.2014.05.011openalex-snapshot
Synthesis and evaluation of (E)-2-(acrylamido)cyclohex-1-enecarboxylic acid derivatives as HCA1, HCA2, and HCA3 receptor agonists
inferred← citeshttps://doi.org/10.1016/j.bmc.2022.116963openalex-snapshot
Design and Synthesis of Novel Pipernonaline Derivatives as Anti-Austerity Agents Against Human Pancreatic Cancer PANC-1 Cells
inferred← citeshttps://doi.org/10.1016/j.bmcl.2009.01.029openalex-snapshot
Pseurotin A and its analogues as inhibitors of immunoglobuline E production
inferred← citeshttps://doi.org/10.1016/j.bmcl.2019.05.042openalex-snapshot
Revisiting microtubule targeting agents: α-Tubulin and the pironetin binding site as unexplored targets for cancer therapeutics
inferred← citeshttps://doi.org/10.1016/j.ejmech.2010.03.003openalex-snapshot
Efficient synthesis and identification of novel propane-1,3-diamino bridged CCR5 antagonists with variation on the basic center carrier
inferred← citeshttps://doi.org/10.1016/j.molcata.2005.02.019openalex-snapshot
Wadsworth–Emmons reactions catalyzed by nanocrystalline MgO
inferred← citeshttps://doi.org/10.1016/j.phytochem.2012.08.001openalex-snapshot
Key structural features of cis-cinnamic acid as an allelochemical
inferred← citeshttps://doi.org/10.1016/j.phytochem.2013.08.013openalex-snapshot
Substituent effects of cis-cinnamic acid analogues as plant growh inhibitors
inferred← citeshttps://doi.org/10.1016/j.tet.2003.09.021openalex-snapshot
A convergent total synthesis of epolactaene: an application of the bridgehead oxiranyl anion strategy
inferred← citeshttps://doi.org/10.1016/j.tet.2005.06.080openalex-snapshot
Oxidative addition of N-halosuccinimides to palladium(0): the discovery of neutral palladium(II) imidate complexes, which enhance Stille coupling of allylic and benzylic halides
inferred← citeshttps://doi.org/10.1016/j.tet.2005.07.106openalex-snapshot
A convergent and stereoselective synthesis of a seco-precursor of macrolactin A
inferred← citeshttps://doi.org/10.1016/j.tet.2006.01.052openalex-snapshot
An efficient synthesis of (E)-α,β-unsaturated ketones and esters with total stereoselectivity by using chromium dichloride
inferred← citeshttps://doi.org/10.1016/j.tet.2008.01.139openalex-snapshot
Asymmetric total synthesis of the myxobacteria metabolites crocacins A–D
inferred← citeshttps://doi.org/10.1016/j.tet.2010.03.080openalex-snapshot
A new bis(pyrenyl)azadiene-based probe for the colorimetric and fluorescent sensing of Cu(II) and Hg(II)
inferred← citeshttps://doi.org/10.1016/j.tet.2010.06.074openalex-snapshot
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inferred← citeshttps://doi.org/10.1016/j.tet.2010.10.034openalex-snapshot
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inferred← citeshttps://doi.org/10.1016/j.tet.2010.11.017openalex-snapshot
Synthetic studies on goniodomin A: convergent assembly of the C15–C36 segment via palladium-catalyzed organostannane–thioester coupling
inferred← citeshttps://doi.org/10.1016/j.tet.2012.11.077openalex-snapshot
Asymmetric total syntheses of xanthatin and 11,13-dihydroxanthatin using a stereocontrolled conjugate allylation to γ-butenolide
inferred← citeshttps://doi.org/10.1016/j.tet.2014.02.072openalex-snapshot
Asymmetric synthesis of naturally occurring nonenolide xyolide through cross metathesis and macrolactonization reaction
inferred← citeshttps://doi.org/10.1016/j.tet.2014.04.037openalex-snapshot
Synthesis of the stabilized active metabolite of clopidogrel
inferred← citeshttps://doi.org/10.1016/j.tet.2016.08.060openalex-snapshot
Synthesis of fluorescent molecular probes based on cis-cinnamic acid and molecular imaging of lettuce roots
inferred← citeshttps://doi.org/10.1016/j.tetasy.2007.03.019openalex-snapshot
Synthetic studies aimed at the elucidation of the stereostructure of the aggregation pheromone, 2-methyl-6-(4′-methylenebicyclo[3.1.0]hexyl)hept-2-en-1-ol, produced by the male stink bug Erysarcoris lewisi
inferred← citeshttps://doi.org/10.1016/j.tetasy.2007.04.008openalex-snapshot
Enantioselective synthesis of tarchonanthuslactone using proline-catalyzed asymmetric α-aminooxylation
inferred← citeshttps://doi.org/10.1016/j.tetasy.2007.09.033openalex-snapshot
A convenient method for the preparation of chiral phosphonoacetamides and their Horner–Wadsworth–Emmons reaction
inferred← citeshttps://doi.org/10.1016/j.tetasy.2010.07.026openalex-snapshot
First asymmetric synthesis of achaetolide
inferred← citeshttps://doi.org/10.1016/j.tetasy.2012.06.015openalex-snapshot
A chemoenzymatic asymmetric synthesis of (+)-strictifolione
inferred← citeshttps://doi.org/10.1016/j.tetasy.2015.03.001openalex-snapshot
A concise enantioselective synthesis of marine macrolide-stagonolide E via organocatalysis
inferred← citeshttps://doi.org/10.1016/j.tetasy.2016.06.002openalex-snapshot
Olefin cross-metathesis based approach for the first total synthesis of phomopsolidone B and total synthesis of phomopsolidone A
inferred← citeshttps://doi.org/10.1016/j.tetlet.2003.08.095openalex-snapshot
A comparison of the Still–Gennari and Ando HWE-methodologies with α,β-unsaturated aldehydes; unexpected results with stannyl substituted systems
inferred← citeshttps://doi.org/10.1016/j.tetlet.2004.02.011openalex-snapshot
Synthesis of (E)-α,β-unsaturated esters with total diastereoselectivity by using chromium dichloride
inferred← citeshttps://doi.org/10.1016/j.tetlet.2004.02.138openalex-snapshot
New solid-supported phosphonate reagents for the synthesis of Z-α,β-unsaturated esters
inferred← citeshttps://doi.org/10.1016/j.tetlet.2004.05.026openalex-snapshot
New and efficient conditions for the Z -selective synthesis of unsaturated esters by the Horner-Wadsworth-Emmons olefination
inferred← citeshttps://doi.org/10.1016/j.tetlet.2004.12.064openalex-snapshot
Diastereoselective addition of silyl metals to γ-alkoxy substituted α,β-unsaturated esters
inferred← citeshttps://doi.org/10.1016/j.tetlet.2005.04.031openalex-snapshot
A carbohydrate-based approach for the total synthesis of strictifolione
inferred← citeshttps://doi.org/10.1016/j.tetlet.2005.07.029openalex-snapshot
A practical synthesis of (−)-kazusamycin A (revised)
inferred← citeshttps://doi.org/10.1016/j.tetlet.2005.09.106openalex-snapshot
General synthetic approach to bicyclo[9.3.0]tetradecenone: a versatile intermediate to clavulactone and clavirolides
inferred← citeshttps://doi.org/10.1016/j.tetlet.2006.05.135openalex-snapshot
A stereoselective synthesis of the C11–C19 fragment of (+)-peloruside A
inferred← citeshttps://doi.org/10.1016/j.tetlet.2006.11.135openalex-snapshot
An enantiospecific synthesis of (+)-isoparvifolinone and (−)-parvifoline
inferred← citeshttps://doi.org/10.1016/j.tetlet.2007.07.172openalex-snapshot
A convergent approach for the total synthesis of (−)-synrotolide diacetate
inferred← citeshttps://doi.org/10.1016/j.tetlet.2007.10.141openalex-snapshot
A practical and enantiospecific conversion of d-galactose to a substituted α,β-unsaturated δ-lactone synthon
inferred← citeshttps://doi.org/10.1016/j.tetlet.2007.11.107openalex-snapshot
Stereoconvergent synthesis of the C1–C11 and C12–C24 fragments of (−)-macrolactin-A
inferred← citeshttps://doi.org/10.1016/j.tetlet.2008.07.027openalex-snapshot
First stereoselective total synthesis of (+)-dodoneine
inferred← citeshttps://doi.org/10.1016/j.tetlet.2009.03.026openalex-snapshot
A facile synthesis of 5,6-dihydro-5-hydroxy-2(1H)-pyridone
inferred← citeshttps://doi.org/10.1016/j.tetlet.2009.07.130openalex-snapshot
Bis(2-t-butylphenyl)phosphonoacetamides for the highly cis-selective synthesis of α,β-unsaturated amides
inferred← citeshttps://doi.org/10.1016/j.tetlet.2010.02.070openalex-snapshot
Stereoselective total synthesis of (+)-polyrhacitide A
inferred← citeshttps://doi.org/10.1016/j.tetlet.2010.02.113openalex-snapshot
New polymer-supported phosphonate reagents for the synthesis of Z-α,β-unsaturated esters
inferred← citeshttps://doi.org/10.1016/j.tetlet.2010.04.072openalex-snapshot
Solvent-free Horner–Wadsworth–Emmons reaction using DBU
inferred← citeshttps://doi.org/10.1016/j.tetlet.2010.09.072openalex-snapshot
Stereoselective total synthesis of stagonolide E
inferred← citeshttps://doi.org/10.1016/j.tetlet.2011.01.043openalex-snapshot
Z-Selective intramolecular Horner–Wadsworth–Emmons reaction for the synthesis of macrocyclic alkenes
inferred← citeshttps://doi.org/10.1016/j.tetlet.2011.12.119openalex-snapshot
Total synthesis of stagonolide B
inferred← citeshttps://doi.org/10.1016/j.tetlet.2012.06.028openalex-snapshot
Synthesis of 1-aminopyrrolizidine alkaloid (−)-absouline by stereoselective aminoconjugate addition
inferred← citeshttps://doi.org/10.1016/j.tetlet.2012.08.019openalex-snapshot
An efficient chiral-pool synthesis of botryolide-E
inferred← citeshttps://doi.org/10.1016/j.tetlet.2012.09.114openalex-snapshot
Synthesis of dialkyl and diaryl benzylphosphonates through a ZnI2-mediated reaction
inferred← citeshttps://doi.org/10.1016/j.tetlet.2013.02.020openalex-snapshot
Highly Z-selective synthesis of α,β-unsaturated nitriles using the Horner–Wadsworth–Emmons reaction
inferred← citeshttps://doi.org/10.1016/j.tetlet.2013.12.110openalex-snapshot
Highly stereoselective Michael reduction/intramolecular Michael reaction cascade to synthesize trans-stereodiad comprising an all-carbon quaternary stereogenic center
inferred← citeshttps://doi.org/10.1016/j.tetlet.2014.05.109openalex-snapshot
Synthesis of four diastereomers and structural revision of tetradenolide
inferred← citeshttps://doi.org/10.1016/j.tetlet.2014.09.124openalex-snapshot
Stereoselective synthesis of C17–C34 fragment of antascomicin A
inferred← citeshttps://doi.org/10.1016/j.tetlet.2015.10.046openalex-snapshot
Synthetic study of arenicolide C: stereoselective synthesis of the C19–C36 segment
inferred← citeshttps://doi.org/10.1016/j.tetlet.2016.03.094openalex-snapshot
Synthesis and absolute configuration of formosusin A, a specific inhibitor of mammalian DNA polymerase β
inferred← citeshttps://doi.org/10.1016/j.tetlet.2018.02.076openalex-snapshot
The formal synthesis of lucentamycin A: Construction of cis -2,3-disubstituted pyrrolidine core by application of SmI 2 -DMPU system
inferred← citeshttps://doi.org/10.1016/j.tetlet.2019.06.058openalex-snapshot
Total synthesis of the tricyclic humulanolide wilfolide B
inferred← citeshttps://doi.org/10.1016/j.tetlet.2025.155708openalex-snapshot
Synthesis of C22-C28 substituted Tetrahydropyran fragment of Eribulin
inferred← citeshttps://doi.org/10.1016/s0021-9517(03)00080-0openalex-snapshot
Wadsworth–Emmons reaction: the unique catalytic reaction by a solid base
inferred← citeshttps://doi.org/10.1016/s0022-1139(01)00452-3openalex-snapshot
Stereoselective synthesis of 3-trifluoromethyl-2E, 4E-dienyl carboxylates
inferred← citeshttps://doi.org/10.1016/s0022-1139(98)00108-0openalex-snapshot
Highly stereoselective synthesis of tetrasubstituted perfluoroalkylated (Z)-α,β-unsaturated esters
inferred← citeshttps://doi.org/10.1016/s0022-328x(02)01370-0openalex-snapshot
Iridium complex-catalyzed carbonylation of allylic phosphates
inferred← citeshttps://doi.org/10.1016/s0040-4020(01)00007-2openalex-snapshot
The Horner–Wadsworth–Emmons reaction of mixed phosphonoacetates and aromatic aldehydes: geometrical selectivity and computational investigation
inferred← citeshttps://doi.org/10.1016/s0040-4020(01)00606-8openalex-snapshot
Stereoselective aldol reaction of α-seleno carbonyl compounds: preparation of (Z)-α,β-unsaturated carbonyl compounds
inferred← citeshttps://doi.org/10.1016/s0040-4020(01)00782-7openalex-snapshot
P(RNCH2CH2)3N: an efficient promoter for the direct synthesis of E-α,β-unsaturated esters
inferred← citeshttps://doi.org/10.1016/s0040-4020(02)01407-2openalex-snapshot
Stereospecific stilbene formation from β-hydroxy-α,β-diphenylethylphosphoranes. Mechanistic proposals based upon stereochemistry
inferred← citeshttps://doi.org/10.1016/s0040-4020(03)00348-xopenalex-snapshot
Synthesis of eleven-membered carbocycles via a homo-Cope type of five-carbon ring expansion reaction utilized β-(hydroxymethyl)allylsilane
inferred← citeshttps://doi.org/10.1016/s0040-4020(97)10305-2openalex-snapshot
Synthesis of nonracemic phosphonates
inferred← citeshttps://doi.org/10.1016/s0040-4020(97)10433-1openalex-snapshot
A new approach to the synthesis of functionalized 1-alkenyl-1H-1,2,3-triazoles
inferred← citeshttps://doi.org/10.1016/s0040-4039(02)02200-1openalex-snapshot
Synthesis of C1C11 fragment of callystatin A
inferred← citeshttps://doi.org/10.1016/s0040-4039(03)00935-3openalex-snapshot
Excess sodium ions improve Z selectivity in Horner–Wadsworth–Emmons olefinations with the Ando phosphonate
inferred← citeshttps://doi.org/10.1016/s0040-4039(97)10428-2openalex-snapshot
Versatile stereocontrol in kinetic resolution of a diphenylphosphinyl-protected α-amino aldehyde by reaction with chiral phosphonates
inferred← citeshttps://doi.org/10.1016/s0040-4039(98)01329-xopenalex-snapshot
A new bisphosphonate reagent for the synthesis of (Z)-olefins and bis(trifluoroethyl) phosphonates
inferred← citeshttps://doi.org/10.1016/s0040-4039(99)02126-7openalex-snapshot
Total synthesis of 6-epi-sarsolilide A
inferred← citeshttps://doi.org/10.1016/s0040-4039(99)02169-3openalex-snapshot
An efficient and stereoselective construction of the C(9)–C(17) dihydropyran segment of swinholides A–C via a novel reductive cleavage of an epoxy aldehyde
inferred← citeshttps://doi.org/10.1016/s0957-4166(99)00316-xopenalex-snapshot
A stereocontrolled synthesis of (−)-detoxinine from l-ascorbic acid
inferred← citeshttps://doi.org/10.1016/s1572-5995(05)80029-8openalex-snapshot
Synthetic Routes to Discodermolide and Pironetin: Two Immunosuppressive and Antitumoral Agents
inferred← citeshttps://doi.org/10.1021/acs.chemrev.6b00488openalex-snapshot
Synthetic Strategies Employed for the Construction of Fostriecin and Related Natural Products
inferred← citeshttps://doi.org/10.1021/acs.iecr.3c00407openalex-snapshot
Wadsworth–Emmons Reaction by Using the Fluorapatite Catalyst: Kinetic Studies
inferred← citeshttps://doi.org/10.1021/acs.inorgchem.2c04221openalex-snapshot
Highly Tunable 4-Phosphoryl Pyrazolone Receptors for Selective Rare-Earth Separation
inferred← citeshttps://doi.org/10.1021/acs.jmedchem.5c02090openalex-snapshot
Amide-to-Chloroalkene Substitution for Peptide Backbone Modification to Enhance Membrane Permeability
inferred← citeshttps://doi.org/10.1021/acs.jnatprod.2c00469openalex-snapshot
Synthesis and Configuration Confirmation of the ATHOD Fatty Amino Acid Residue in the Burkholdines
inferred← citeshttps://doi.org/10.1021/acs.jnatprod.3c00988openalex-snapshot
Total Synthesis, Revised Structure, and Biological Evaluation of Elgonene B and Analogues
inferred← citeshttps://doi.org/10.1021/acs.joc.1c02600openalex-snapshot
Biomimetic Construction of a syn-2,7-Dimethyloxepane Ring via 7-Endo Cyclization
inferred← citeshttps://doi.org/10.1021/acs.joc.2c00763openalex-snapshot
One-Pot O2-Oxidation and the Horner–Wadsworth–Emmons Reaction of Primary Alcohols for the Synthesis of (Z)-α,β-Unsaturated Esters
inferred← citeshttps://doi.org/10.1021/acs.joc.4c02861openalex-snapshot
Synthesis of Phoslactomycin I-i
inferred← citeshttps://doi.org/10.1021/acs.joc.5b02556openalex-snapshot
Aminooxylation Horner–Wadsworth–Emmons Sequence for the Synthesis of Enantioenriched γ-Functionalized Vinyl Sulfones
inferred← citeshttps://doi.org/10.1021/acs.joc.5c00470openalex-snapshot
Z-Selective Synthesis of Trisubstituted Alkenes by the HWE Reaction Using Modified Still–Gennari Type Reagents
inferred← citeshttps://doi.org/10.1021/acs.joc.6b02586openalex-snapshot
Syntheses of Combretastatins D-1, D-2, and D-4 via Ring Contraction by Flash Vacuum Pyrolysis
inferred← citeshttps://doi.org/10.1021/acs.joc.6c00930openalex-snapshot
One-Pot Electrodeprotection and Horner–Wadsworth–Emmons Olefination of Acetals Using LiClO 4 –1,3,5-Trioxane Complex
inferred← citeshttps://doi.org/10.1021/acs.orglett.0c01649openalex-snapshot
Asymmetric Total Syntheses of (+)-Penostatins A and C
inferred← citeshttps://doi.org/10.1021/acs.orglett.4c02239openalex-snapshot
From Acyclic Intramolecular-[4 + 2]- to Transannular Bis-[4 + 2]-Cycloaddition of the Macrodiolide for the Stereoselective Synthesis of the Octahydronaphthalene Core of Polyenic Macrolactam Sagamilactam
inferred← citeshttps://doi.org/10.1021/acs.orglett.5b02681openalex-snapshot
Radical Solution to the Alkylation of the Highly Base-Sensitive 1,1-Dichloroacetone. Application to the Synthesis of Z-Alkenoates and E,E-Dienoates
inferred← citeshttps://doi.org/10.1021/acs.orglett.5b02901openalex-snapshot
Lewis Base Activation of Silyl Acetals: Iridium-Catalyzed Reductive Horner–Wadsworth–Emmons Olefination
inferred← citeshttps://doi.org/10.1021/acs.orglett.5c02194openalex-snapshot
Stereoselective Synthesis of (E)-α-Bromo- and (E)-α-Iodoacrylates from Readily Available tert-Butyl Diphenylphosphonoacetate
inferred← citeshttps://doi.org/10.1021/acs.orglett.5c04440openalex-snapshot
Divergent Total Synthesis of Diterpenoid Natural Products from Salvia miltiorrhiza
inferred← citeshttps://doi.org/10.1021/acs.orglett.6b01524openalex-snapshot
Enantioselective Total Synthesis of RQN-18690A (18-Deoxyherboxidiene)
inferred← citeshttps://doi.org/10.1021/acscentsci.0c00599openalex-snapshot
Unconventional Macrocyclizations in Natural Product Synthesis
inferred← citeshttps://doi.org/10.1021/acssuschemeng.5c06607openalex-snapshot
Deep Investigation of the Effect of DAC Modified by Horner-Wadsworth-Emmons Olefination on the Water Swelling Properties and Strength of Its Hydrogel Composites
inferred← citeshttps://doi.org/10.1021/ar500433topenalex-snapshot
α,β-Unsaturated Diazoketones as Useful Platforms in the Synthesis of Nitrogen Heterocycles
inferred← citeshttps://doi.org/10.1021/cr400126uopenalex-snapshot
Functions, Therapeutic Applications, and Synthesis of Retinoids and Carotenoids
inferred← citeshttps://doi.org/10.1021/ja0005845openalex-snapshot
Novel Pd(II)- and Pt(II)-Catalyzed Regio- and Stereoselective trans -Hydroarylation of Alkynes by Simple Arenes
inferred← citeshttps://doi.org/10.1021/ja0340679openalex-snapshot
Total Synthesis of Leustroducsin B
inferred← citeshttps://doi.org/10.1021/jacs.6c06951openalex-snapshot
Reprogramming ThDP Enzymes for Z -Alkenes: Overriding Thermodynamic Preference via Noncovalent Controls
inferred← citeshttps://doi.org/10.1021/jm100649dopenalex-snapshot
Potent Antagonist for the Vitamin D Receptor: Vitamin D Analogues with Simple Side Chain Structure
inferred← citeshttps://doi.org/10.1021/jm2016914openalex-snapshot
Structure–Activity Relationship Study of a CXC Chemokine Receptor Type 4 Antagonist, FC131, Using a Series of Alkene Dipeptide Isosteres
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