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Total Synthesis of Natural 8- and 9-Membered Lactones: Recent Advancements in Medium-Sized Ring Formation
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inferredcites →https://doi.org/10.1002/anie.200461428openalex-snapshot
Synthesis of the C‐1027 Chromophore Framework through Atropselective Macrolactonization
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Enantioselective Total Synthesis of Octalactin A Using Asymmetric Aldol Reactions and a Rapid Lactonization To Form a Medium‐Sized Ring
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Solandelactones A-I, lactonized cyclopropyl oxylipins isolated from the hydroid Solanderia secunda
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inferredcites →https://doi.org/10.1016/0040-4039(94)85009-7openalex-snapshot
Further studies on oxazoline and thiazoline oxidations. A reliable route to chiral oxazoles and thiazoles
inferredcites →https://doi.org/10.1016/0040-4039(95)00498-2openalex-snapshot
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inferredcites →https://doi.org/10.1016/0040-4039(95)00588-4openalex-snapshot
The total asymmetric synthesis of Halicholactone and Neohalicholactone
inferredcites →https://doi.org/10.1016/0040-4039(96)00512-6openalex-snapshot
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inferredcites →https://doi.org/10.1016/0040-4039(96)01014-3openalex-snapshot
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inferredcites →https://doi.org/10.1016/j.tet.2003.12.013openalex-snapshot
An effective method for the synthesis of carboxylic esters and lactones using substituted benzoic anhydrides with Lewis acid catalysts
inferredcites →https://doi.org/10.1016/j.tet.2006.04.077openalex-snapshot
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inferredcites →https://doi.org/10.1016/j.tetasy.2005.08.042openalex-snapshot
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inferredcites →https://doi.org/10.1016/j.tetlet.2003.10.213openalex-snapshot
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inferredcites →https://doi.org/10.1016/j.tetlet.2005.12.031openalex-snapshot
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inferredcites →https://doi.org/10.1016/j.tetlet.2006.01.140openalex-snapshot
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inferredcites →https://doi.org/10.1016/s0040-4020(01)80533-0openalex-snapshot
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inferredcites →https://doi.org/10.1016/s0040-4020(01)85585-xopenalex-snapshot
Stereoselective synthesis of erythronolide a by extremely efficient lactonization based on conformational adjustment and high activation of seco-acid1
inferredcites →https://doi.org/10.1016/s0040-4020(01)85653-2openalex-snapshot
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inferredcites →https://doi.org/10.1016/s0040-4020(01)86136-6openalex-snapshot
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inferredcites →https://doi.org/10.1016/s0040-4020(01)86869-1openalex-snapshot
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inferredcites →https://doi.org/10.1016/s0040-4020(01)91380-8openalex-snapshot
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inferredcites →https://doi.org/10.1016/s0040-4020(97)10427-6openalex-snapshot
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inferredcites →https://doi.org/10.1016/s0040-4039(00)00434-2openalex-snapshot
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inferredcites →https://doi.org/10.1016/s0040-4039(00)01808-6openalex-snapshot
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inferredcites →https://doi.org/10.1016/s0040-4039(00)61908-1openalex-snapshot
Preparation of chiral cyclohexanol derivative with high optical purity by yeast reduction
inferredcites →https://doi.org/10.1016/s0040-4039(00)74344-9openalex-snapshot
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inferredcites →https://doi.org/10.1016/s0040-4039(00)79490-1openalex-snapshot
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inferredcites →https://doi.org/10.1016/s0040-4039(00)82884-1openalex-snapshot
Stereoselective reduction of β-alkoxy ketones: a synthesis of syn-1,3-diols
inferredcites →https://doi.org/10.1016/s0040-4039(00)83907-6openalex-snapshot
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inferredcites →https://doi.org/10.1016/s0040-4039(00)85417-9openalex-snapshot
Studies on the synthesis of gloeosporone - synthesis of the proposed 2,8-disubstituted oxocane structure
inferredcites →https://doi.org/10.1016/s0040-4039(00)93056-9openalex-snapshot
Mechanistic studies on the double activation method for the synthesis of macrocyclic lactones
inferredcites →https://doi.org/10.1016/s0040-4039(00)93057-0openalex-snapshot
New reagents for the conversion of hydroxy acids to macrolactones by the double activation method
inferredcites →https://doi.org/10.1016/s0040-4039(00)94040-1openalex-snapshot
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inferredcites →https://doi.org/10.1016/s0040-4039(00)94489-7openalex-snapshot
Convenient synthesis of chiral epoxyisoprenoids by yeast reduction
inferredcites →https://doi.org/10.1016/s0040-4039(00)96375-5openalex-snapshot
A synthesis of pseudo-gloeosporone
inferredcites →https://doi.org/10.1016/s0040-4039(00)99112-3openalex-snapshot
Ascidiatrienolids A-C, novel lactonized eicosanoids from the colonial marine ascidian Didemnum candidum
inferredcites →https://doi.org/10.1016/s0040-4039(01)01238-2openalex-snapshot
Enantioselective synthesis of β-hydroxy-α-methyl-α-methylthio esters as precursors of anti-vic-hydroxymethyl units
inferredcites →https://doi.org/10.1016/s0040-4039(01)02078-0openalex-snapshot
Total synthesis of octalactin A via ring-closing metathesis reaction
inferredcites →https://doi.org/10.1016/s0040-4039(01)80205-7openalex-snapshot
Horner-wadsworth-emmons reaction: Use of lithium chloride and an amine for base-sensitive compounds
inferredcites →https://doi.org/10.1016/s0040-4039(01)80740-1openalex-snapshot
Halicholactone and neohalicholactone, two novel fatty acid metabolites from the marine sponge kadota
inferredcites →https://doi.org/10.1016/s0040-4039(01)81188-6openalex-snapshot
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inferredcites →https://doi.org/10.1016/s0040-4039(01)94789-6openalex-snapshot
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inferredcites →https://doi.org/10.1016/s0040-4039(01)95937-4openalex-snapshot
Structure of vermiculine, a new nine-membered lactone from penicillium vermiculatum
inferredcites →https://doi.org/10.1016/s0040-4039(02)01557-5openalex-snapshot
Synthesis of polypropionate motifs containing the anti–anti unit
inferredcites →https://doi.org/10.1016/s0040-4039(02)01819-1openalex-snapshot
A novel and efficient macrolactonization of ω-hydroxycarboxylic acids using 2-methyl-6-nitrobenzoic anhydride (MNBA)
inferredcites →https://doi.org/10.1016/s0040-4039(97)10127-7openalex-snapshot
Studies towards the synthesis of the marine metabolite, octalactin A
inferredcites →https://doi.org/10.1016/s0040-4039(97)10731-6openalex-snapshot
Studies towards the total syntheses of solandelactones: Stereoselective synthesis of the cyclopropane - lactone segment
inferredcites →https://doi.org/10.1016/s0040-4039(98)01420-8openalex-snapshot
Stereoselective reduction of α′-branched α,β-ynones. Application to the synthesis of the Octalactin A ring
inferredcites →https://doi.org/10.1016/s0040-4039(99)01070-9openalex-snapshot
Catalytic asymmetric vinylogous Mukaiyama (CAVM) reactions: aldehyde activation versus enolate activation
inferredcites →https://doi.org/10.1016/s0040-4039(99)01988-7openalex-snapshot
Medium ring stereocontrol in the functionalisation of eight-membered lactones
inferredcites →https://doi.org/10.1016/s0957-4166(00)86005-xopenalex-snapshot
Enantioselective reduction of acetophenone with 1,3,2-oxazaborolidines derived from ephedrine, pseudoephedrine, and phenylglycine
inferredcites →https://doi.org/10.1016/s0957-4166(00)86116-9openalex-snapshot
Catalytic asymmetric aldol reaction of the silyl enol ether of acetic acid thioester with aldehydes using chiral tin(II) Lewis acid
inferredcites →https://doi.org/10.1016/s0957-4166(00)86163-7openalex-snapshot
Enantioselective reduction of ketones catalysed by 1,3,2-oxazaborolidines prepared from phenylglycine
inferredcites →https://doi.org/10.1016/s0957-4166(98)00413-3openalex-snapshot
A chiron approach to the cyclopropyl lactone oxylipins
inferredcites →https://doi.org/10.1021/ar00064a001openalex-snapshot
Ring closure reactions of bifunctional chain molecules
inferredcites →https://doi.org/10.1021/cen-v030n007.p612openalex-snapshot
121st National Meeting American Chemical Society
inferredcites →https://doi.org/10.1021/cr00013a003openalex-snapshot
Chiral titanium complexes for enantioselective addition of nucleophiles to carbonyl groups
inferredcites →https://doi.org/10.1021/cr00038a012openalex-snapshot
Total Synthesis of Bioactive Marine Macrolides
inferredcites →https://doi.org/10.1021/cr0301402openalex-snapshot
Macrolactonizations in the Total Synthesis of Natural Products
inferredcites →https://doi.org/10.1021/ja00011a030openalex-snapshot
Asymmetric aldol reaction between achiral silyl enol ethers and achiral aldehydes by use of a chiral promoter system
inferredcites →https://doi.org/10.1021/ja00012a048openalex-snapshot
Octalactins A and B: cytotoxic eight-membered-ring lactones from a marine bacterium, Streptomyces sp
inferredcites →https://doi.org/10.1021/ja00033a005openalex-snapshot
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inferredcites →https://doi.org/10.1021/ja00046a062openalex-snapshot
Internal redox catalyzed by triphenylphosphine
inferredcites →https://doi.org/10.1021/ja00066a056openalex-snapshot
Ascidiatrienolide A is a 10-membered lactone
inferredcites →https://doi.org/10.1021/ja00091a082openalex-snapshot
Total Synthesis of Octalactin A and B
inferredcites →https://doi.org/10.1021/ja00097a060openalex-snapshot
Total Synthesis of (+)-Octalactins A and B: Unusual Metabolites from a Marine Microbe
inferredcites →https://doi.org/10.1021/ja001179gopenalex-snapshot
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inferredcites →https://doi.org/10.1021/ja00173a013openalex-snapshot
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inferredcites →https://doi.org/10.1021/ja00173a071openalex-snapshot
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inferredcites →https://doi.org/10.1021/ja00175a043openalex-snapshot
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inferredcites →https://doi.org/10.1021/ja00190a034openalex-snapshot
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inferredcites →https://doi.org/10.1021/ja00219a035openalex-snapshot
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inferredcites →https://doi.org/10.1021/ja00226a041openalex-snapshot
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inferredcites →https://doi.org/10.1021/ja00257a034openalex-snapshot
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inferredcites →https://doi.org/10.1021/ja00262a017openalex-snapshot
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inferredcites →https://doi.org/10.1021/ja00263a020openalex-snapshot
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inferredcites →https://doi.org/10.1021/ja00396a051openalex-snapshot
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inferredcites →https://doi.org/10.1021/ja00417a033openalex-snapshot
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inferredcites →https://doi.org/10.1021/ja00423a046openalex-snapshot
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inferredcites →https://doi.org/10.1021/ja00462a049openalex-snapshot
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inferredcites →https://doi.org/10.1021/ja00538a077openalex-snapshot
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inferredcites →https://doi.org/10.1021/ja00795a055openalex-snapshot
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inferredcites →https://doi.org/10.1021/ja00824a073openalex-snapshot
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inferredcites →https://doi.org/10.1021/ja00825a054openalex-snapshot
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inferredcites →https://doi.org/10.1021/ja00845a037openalex-snapshot
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inferredcites →https://doi.org/10.1021/ja00845a038openalex-snapshot
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inferredcites →https://doi.org/10.1021/ja00845a039openalex-snapshot
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inferredcites →https://doi.org/10.1021/ja010805mopenalex-snapshot
Synthesis of Propionate Motifs: Diastereoselective Tandem Reactions Involving Anionic and Free Radical Based Processes
inferredcites →https://doi.org/10.1021/ja01101a027openalex-snapshot
The Chemistry of Antimycin A. II. Degradation Studies1
inferredcites →https://doi.org/10.1021/ja01175a057openalex-snapshot
The Isolation and Properties of Antimycin A
inferredcites →https://doi.org/10.1021/ja01468a023openalex-snapshot
The Chemistry of Antimycin A. X. Structure of the Antimycins1
inferredcites →https://doi.org/10.1021/ja038353wopenalex-snapshot
A Concise Synthesis of the Octalactins
inferredcites →https://doi.org/10.1021/ja046389yopenalex-snapshot
Synthesis of Postulated Molecular Probes: Stereoselective Free-Radical-Mediated C-Glycosylation in Tandem with Hydrogen Transfer
inferredcites →https://doi.org/10.1021/ja954312ropenalex-snapshot
Total Synthesis of Streptogramin Antibiotics. (−)-Madumycin II
inferredcites →https://doi.org/10.1021/ja962345gopenalex-snapshot
An Efficient Asymmetric Epoxidation Method for trans-Olefins Mediated by a Fructose-Derived Ketone
inferredcites →https://doi.org/10.1021/ja9709132openalex-snapshot
Synthesis of Medium Ring Ethers. 5. The Synthesis of (+)-Laurencin
inferredcites →https://doi.org/10.1021/ja972064oopenalex-snapshot
The Exo-Cyclic Effect: Strategy Employing in Situ Derivatization or Lewis Acid Complexation to Enhance Stereoselectivity in Hydrogen Transfer Reactions
inferredcites →https://doi.org/10.1021/ja972272gopenalex-snapshot
An Efficient Catalytic Asymmetric Epoxidation Method
inferredcites →https://doi.org/10.1021/jm9706574openalex-snapshot
Enantiospecific Semisynthesis of (+)-Almuheptolide-A, a Novel Natural Heptolide Inhibitor of the Mammalian Mitochondrial Respiratory Chain
inferredcites →https://doi.org/10.1021/jo00020a007openalex-snapshot
Enantioselective Michael reactions. Diastereoselective reactions of chlorotitanium enolates of chiral N-acyloxazolidinones with representative electrophilic olefins
inferredcites →https://doi.org/10.1021/jo00023a001openalex-snapshot
Stereospecific methylation of .gamma.,.delta.-epoxy acrylates by trimethylaluminum: a method for the iterative construction of polypropionate chains
inferredcites →https://doi.org/10.1021/jo00077a009openalex-snapshot
Aqueous reactions with a Lewis acid and an organometallic reagent. The scandium trifluoromethanesulfonate-catalyzed allylation reaction of carbonyl compounds with tetraallyltin
inferredcites →https://doi.org/10.1021/jo001036copenalex-snapshot
Asymmetric Total Synthesis of Halicholactone
inferredcites →https://doi.org/10.1021/jo00109a049openalex-snapshot
Improved Procedure for the Synthesis of Enantiomerically Enriched Cyclopropylmethanol Derivatives
inferredcites →https://doi.org/10.1021/jo00213a044openalex-snapshot
Proton-transfer steps in Steglich esterification: a very practical new method for macrolactonization
inferredcites →https://doi.org/10.1021/jo00265a033openalex-snapshot
Total synthesis of (+)-colletodiol: new methodology for the synthesis of macrolactones
inferredcites →https://doi.org/10.1021/jo00288a004openalex-snapshot
Chiral synthesis of polyketide-derived natural products. 27. Stereoselective synthesis of erythronolide A via an extremely efficient macrolactonization by the modified Yamaguchi method
inferredcites →https://doi.org/10.1021/jo00376a052openalex-snapshot
Electrophilic sulfur transfer reactions in organic synthesis. Preparation of a diastereomer of the key macrocyclic component of griseoviridin
inferredcites →https://doi.org/10.1021/jo00809a014openalex-snapshot
Reactions of dimethylphosphono-substituted diazoalkanes. (MeO)2P(O)CR transfer to olefins and 1,3-dipolar additions of (MeO)2P(O)C(N2)R
inferredcites →https://doi.org/10.1021/jo00879a039openalex-snapshot
Stereoselective synthesis of vinylsilanes from alkynylsilanes by reductive alkylation via hydroboration and carbodemetalation
inferredcites →https://doi.org/10.1021/jo015567sopenalex-snapshot
Catalytic Asymmetric Vinylogous Mukaiyama-Aldol (CAVM) Reactions: The Enolate Activation
inferredcites →https://doi.org/10.1021/jo030367xopenalex-snapshot
An Effective Use of Benzoic Anhydride and Its Derivatives for the Synthesis of Carboxylic Esters and Lactones: A Powerful and Convenient Mixed Anhydride Method Promoted by Basic Catalysts
inferredcites →https://doi.org/10.1021/jo034195fopenalex-snapshot
Approaches toward the Total Synthesis of the Nine-Membered Thio-Lactone Core of Griseoviridin
inferredcites →https://doi.org/10.1021/jo034901copenalex-snapshot
Regulated-Stereoselective Construction of Thirteen Stereogenic Centers Necessary for the Frame of (+)-Discodermolide, Based on Iterative Lewis Acid-Promoted Aldol Reactions
inferredcites →https://doi.org/10.1021/jo051993sopenalex-snapshot
Biosynthetic Studies on the Botcinolide Skeleton: New Hydroxylated Lactones from Botrytis cinerea
inferredcites →https://doi.org/10.1021/jo0604890openalex-snapshot
An Expeditious Enantioselective Synthesis of Antimycin A3b
inferredcites →https://doi.org/10.1021/jo952237xopenalex-snapshot
Scandium Trifluoromethanesulfonate as an Extremely Active Lewis Acid Catalyst in Acylation of Alcohols with Acid Anhydrides and Mixed Anhydrides
inferredcites →https://doi.org/10.1021/jo962312jopenalex-snapshot
Total Synthesis of Halicholactone and Neohalicholactone1
inferredcites →https://doi.org/10.1021/jo971564xopenalex-snapshot
Stereoselective Synthesis of a Key Precursor of Halicholactone and Neohalicholactone
inferredcites →https://doi.org/10.1021/jo9721195openalex-snapshot
Highly Regio- and Enantioselective Monoepoxidation of Conjugated Dienes
inferredcites →https://doi.org/10.1021/np020471uopenalex-snapshot
New Sesterterpene Metabolites from the Mediterranean Sponge Cacospongia scalaris
inferredcites →https://doi.org/10.1021/np0503855openalex-snapshot
Botcinins A, B, C, and D, Metabolites Produced by Botrytis c inerea , and Their Antifungal Activity against Magnaporthe g risea , a Pathogen of Rice Blast Disease
inferredcites →https://doi.org/10.1021/np060071xopenalex-snapshot
Botcinins E and F and Botcinolide from Botrytis c inerea and Structural Revision of Botcinolides
inferredcites →https://doi.org/10.1021/np50114a016openalex-snapshot
Absolute Stereochemistry of Neohalicholactone from the Brown Alga Laminaria sinclairii
inferredcites →https://doi.org/10.1021/ol015758hopenalex-snapshot
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inferredcites →https://doi.org/10.1021/ol025605+openalex-snapshot
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inferredcites →https://doi.org/10.1021/ol034944fopenalex-snapshot
Efficient Two-Step Conversion of α,β-Unsaturated Aldehydes to Optically Active γ-Oxy-α,β-unsaturated Nitriles and Its Application to the Total Synthesis of (+)-Patulolide C
inferredcites →https://doi.org/10.1021/ol062011oopenalex-snapshot
The First Total Synthesis of (−) and (+)-2-Hydroxy-24-oxooctacosanolide Using an Effective Lactonization
inferredcites →https://doi.org/10.1021/ol062058+openalex-snapshot
Stereoselective Total Synthesis of the Proposed Structure of 2-Epibotcinolide
inferredcites →https://doi.org/10.1039/b517385jopenalex-snapshot
Total synthesis of floresolide B and Δ6,7-Z-floresolide B
inferredcites →https://doi.org/10.1039/c39950000139openalex-snapshot
Synthesis and X-ray crystallographic structure of the right-hand hemisphere of halicholactone and neohalicholactone
inferredcites →https://doi.org/10.1039/p19760001996openalex-snapshot
Revised constitution, absolute configuration, and conformation of griseoviridin, a modified cyclic peptide antibiotic
inferredcites →https://doi.org/10.1039/p19850000843openalex-snapshot
Structures of the cephalosporolides B–F, a group of C 10 lactones from Cephalosporium aphidicola
inferredcites →https://doi.org/10.1055/s-1981-29317openalex-snapshot
The Use of Diethyl Azodicarboxylate and Triphenylphosphine in Synthesis and Transformation of Natural Products
inferredcites →https://doi.org/10.1055/s-1998-1618openalex-snapshot
Hydrogen and Allylation Transfer Reactions in Acyclic Free Radicals
inferredcites →https://doi.org/10.1055/s-1998-1778openalex-snapshot
A New Stereoselective Route to (-)-Octalactin A Based on Intramolecular SmI2 Promoted Reformatsky Reaction
inferredcites →https://doi.org/10.1055/s-2000-6491openalex-snapshot
Towards the Total Synthesis of Octalactin A
inferredcites →https://doi.org/10.1055/s-2002-34233openalex-snapshot
Chiral Titanium Complexes. Synthesis of Optically Active Unsaturated Alcohols, Diols, Polypropionates and their Use in the Synthesis of Biologically Active Compounds
inferredcites →https://doi.org/10.1081/scc-100104408openalex-snapshot
FACILE SYNTHESIS OF SATURATED EIGHT-MEMBERED RING LACTONES
inferredcites →https://doi.org/10.1111/j.1439-0434.2004.00896.xopenalex-snapshot
Virulence–Toxin Production Relationship in Isolates of the Plant Pathogenic Fungus Botrytis cinerea
inferredcites →https://doi.org/10.1246/bcsj.43.2632openalex-snapshot
A Convenient Method for the Preparation of Thiolesters
inferredcites →https://doi.org/10.1246/bcsj.49.779openalex-snapshot
The Michael Reaction of Silyl Enol Ethers with α,β-Unsaturated Eetones and Acetals in the Presence of Titanium Tetraalkoxide and Titanium Tetrachloride
inferredcites →https://doi.org/10.1246/bcsj.50.1863openalex-snapshot
New Method for the Preparation of Carboxylic Esters
inferredcites →https://doi.org/10.1246/bcsj.52.1989openalex-snapshot
A Rapid Esterification by Means of Mixed Anhydride and Its Application to Large-ring Lactonization
inferredcites →https://doi.org/10.1246/bcsj.54.274openalex-snapshot
Aldol Reaction of Aluminium Enolate Resulting from 1,4-Addition of R2AlX to α,β-Unsaturated Carbonyl Compound. A 1-Acylethenyl Anion Equivalent
inferredcites →https://doi.org/10.1246/bcsj.66.1516openalex-snapshot
A New and Efficient Esterification Reaction via Mixed Anhydrides by the Promotion of a Catalytic Amount of Lewis Acid
inferredcites →https://doi.org/10.1246/bcsj.67.1708openalex-snapshot
Diastereo- and Enantioselective Synthesis of syn- and anti-1,2-Diol Units by Asymmetric Aldol Reactions
inferredcites →https://doi.org/10.1246/bcsj.67.210openalex-snapshot
An Effective Method for Acylation of Weakly Nucleophilic Anilines with Silyl Carboxylates via Mixed Anhydrides
inferredcites →https://doi.org/10.1246/bcsj.79.501openalex-snapshot
Exploring the Chemistry and Biology of Antitumor Enediyne Chromoprotein C-1027
inferredcites →https://doi.org/10.1246/cl.1975.1045openalex-snapshot
A CONVENIENT METHOD FOR THE SYNTHESIS OF CARBOXYLIC ESTERS
inferredcites →https://doi.org/10.1246/cl.1990.129openalex-snapshot
Catalytic Asymmetric Aldol Reaction of Silyl Enol Ethers with Aldehydes by the Use of Chiral Diamine Coordinated Tin(II) Triflate
inferredcites →https://doi.org/10.1246/cl.1991.1901openalex-snapshot
Highly Enantioselective Synthesis of syn-α,β-Dihydroxy Thioesters by the Asymmetric Aldol Reaction Using a Chiral Tin(II) Lewis Acid
inferredcites →https://doi.org/10.1246/cl.1992.1747openalex-snapshot
A New and Efficient Method for the Preparation of S-Phenyl Carbothioates via Mixed Anhydrides Using Active Titanium(IV) Salts
inferredcites →https://doi.org/10.1246/cl.1992.373openalex-snapshot
An Efficient Method for the Preparation of Chiral Synthons Starting from Racemic Compounds by Way of Asymmetric Synthesis
inferredcites →https://doi.org/10.1246/cl.1993.1053openalex-snapshot
A Convenient Synthesis of Carboxanilides from Silyl Carboxylates and Weakly Nucleophilic Anilines Using p-Trifluoromethylbenzoic Anhydride and a Catalytic Amount of Active Titanium(IV) Salt
inferredcites →https://doi.org/10.1246/cl.1993.907openalex-snapshot
Facile Synthesis of Lactones from Silyl ω-Siloxycarboxylates Using p-Trifluoromethylbenzoic Anhydride and a Catalytic Amount of Active Lewis Acid
inferredcites →https://doi.org/10.1246/cl.1994.515openalex-snapshot
A Useful Method for the Preparation of Carboxylic Esters from Free Carboxylic Acids and Alcohols
inferredcites →https://doi.org/10.1246/cl.1994.677openalex-snapshot
A Novel Method for the Preparation of Macrolides from ω-Hydroxycarboxylic Acids
inferredcites →https://doi.org/10.1246/cl.1996.1039openalex-snapshot
A Simple Method for the Conversion of Primary Alcohols into Terminal Olefins
inferredcites →https://doi.org/10.1246/cl.1997.117openalex-snapshot
Enantioselective Synthesis of Octalactin A
inferredcites →https://doi.org/10.1246/cl.1998.831openalex-snapshot
Determination of Relative and Absolute Stereochemistry of Cephalosporolide D and Its Enantioselective Total Synthesis
inferredcites →https://doi.org/10.1246/cl.2002.286openalex-snapshot
A New Condensation Reaction for the Synthesis of Carboxylic Esters from Nearly Equimolar Amounts of Carboxylic Acids and Alcohols Using 2-Methyl-6-nitrobenzoic Anhydride
inferredcites →https://doi.org/10.1248/cpb.47.131openalex-snapshot
Revised Structure of Gonioheptolide A.
inferredcites →https://doi.org/10.1271/bbb.57.1980openalex-snapshot
Botcinolide: A Biologically Active Natural Product fromBotrytis cinerea
inferredcites →https://doi.org/10.1271/bbb.60.656openalex-snapshot
Homobotcinolide: A Biologically Active Natural Homolog of Botcinolide fromBotrytis cinerea
inferredcites →https://doi.org/10.1351/pac198254122537openalex-snapshot
Studies on the total synthesis of streptogramin antibiotics: griseoviridin and madumycin (A-2315A)
inferredcites →https://doi.org/10.3987/com-02-s(m)31openalex-snapshot
Solid-Phase Synthesis of 2-(4-Carbamoylpyrazolyl)-4-alkylamino-6-aminopyrimidine Derivatives
inferredcites →https://doi.org/10.3987/com-02-s(m)41openalex-snapshot
Total Synthesis of (-)-Halicholactone
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Incoming claims: where this work appears in other papers’ reference lists and arguments.
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Intramolecular Aerobic Ring Expansion of Cyclic Ketone: A Mild Method for the Synthesis of Medium‐Sized Lactones and Macrolactones
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Direct Access to 9/6‐Fused Cycles via Sequential Hydride Shift Mediated Double C(sp3)−H Bond Functionalization
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Au(I)‐Catalyzed Regiodivergent Hydroarylation of Allenes for the Synthesis of Tetrahydrodiazepines or Tetrahydrodiazonines
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An Enantiodivergent Synthesis of (+)‐ and (−)‐Centrolobines by Asymmetric Esterification Catalyzed by ( R )‐(+)‐ N ‐Methylbenzoguanidine (( R )‐NMBG)
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Fast and Efficient Synthesis of Z‐Enol‐γ‐Lactones through a Cycloisomerization Reaction of β‐Hydroxy‐γ‐Alkynoic Acids Catalyzed by Copper(I) under Microwave Heating in Water
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Lewis Acid‐Catalyzed Stereoselective [7+7] Intermolecular Cyclization of Aniline‐Tethered Alkylidenecyclopropanes: A One‐Step Synthetic Protocol of 14‐Membered Macrocyclic Dimers
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An Efficient Synthesis of 1,3‐Disubstituted Pyrazoles from 2‐Acylaziridines
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Recent Advances in the Synthesis of Fused‐Cyclic Quinolines
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Ring Expansion from 16‐Membered Macrocyclic Lactones Using Yamaguchi and Photoinduced Decarboxylative Radical Macrolactonization
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Recent Advances in Transformation of 1,4‐Diyn‐3‐ones and 1,4‐Diyn‐3‐ols
inferred← citeshttps://doi.org/10.1002/ange.200800554openalex-snapshot
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inferred← citeshttps://doi.org/10.1002/ange.200804576openalex-snapshot
Intermolecular Double Prins‐Type Cyclization: A Facile and Efficient Synthesis of 1,6‐Dioxecanes
inferred← citeshttps://doi.org/10.1002/ange.201200425openalex-snapshot
Tandem Cross‐Dimerisation/Oxonia‐Cope Reaction of Carbonyl Compounds to Homoallylic Esters and Lactones
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Lewis Acid Catalyzed Intramolecular [4+2] and [3+2] Cross‐Cycloaddition of Alkynylcyclopropane Ketones with Carbonyl Compounds and Imines
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Highly Enantioselective Rhodium(I)‐Catalyzed Carbonyl Carboacylations Initiated by CC Bond Activation
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Radical‐Mediated 1,2‐Formyl/Carbonyl Functionalization of Alkenes and Application to the Construction of Medium‐Sized Rings
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A Migratory Ether Formation Route to Medium‐Sized Sugar Mimetics
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Yttrium‐Catalyzed Intramolecular Hydroalkoxylation/Claisen Rearrangement Sequence: Efficient Synthesis of Medium‐Sized Lactams
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Gold‐Catalyzed Double Cycloisomerization of 1‐Ene‐4,10‐diynyl Esters to Bicyclo[6.3.0]undeca‐2,4,9‐trienyl Esters
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Enantioselective Organocatalytic Four‐Atom Ring Expansion of Cyclobutanones: Synthesis of Benzazocinones
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Photocatalytic Aerobic Oxidative Ring Expansion of Cyclic Ketones to Macrolactones by Cerium and Cyanoanthracene Catalysis
inferred← citeshttps://doi.org/10.1002/ange.202105882openalex-snapshot
Macrolactonization Reactions Driven by a Pentafluorobenzoyl Group**
inferred← citeshttps://doi.org/10.1002/ange.202206501openalex-snapshot
Atroposelective Construction of Nine‐Membered Carbonate‐Bridged Biaryls
inferred← citeshttps://doi.org/10.1002/ange.202213676openalex-snapshot
Palladium‐Catalyzed [6+2] Double Allene Annulation for Benzazocines Synthesis
inferred← citeshttps://doi.org/10.1002/ange.202300773openalex-snapshot
Tricrilactones A–H, Potent Antiosteoporosis Macrolides with Distinctive Ring Skeletons from Trichocladium crispatum, an Alpine Moss‐Associated Fungus
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Chromium‐ and Metal‐Reductant‐Free Asymmetric Nozaki–Hiyama–Kishi (NHK) Reaction Enabled by Metallaphotoredox Catalysis
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Catalytic Asymmetric Synthesis of Inherently Chiral Eight‐Membered O‐Heterocycles through Cross‐[4+4] Cycloaddition of Quinone Methides
inferred← citeshttps://doi.org/10.1002/ange.202525903openalex-snapshot
Homologative Radical 1,3‐Dicarbofunctionalization of Unactivated Alkenes Enabled by Sequential Functional Group Migrations
inferred← citeshttps://doi.org/10.1002/ange.8290035openalex-snapshot
Synthesis of Large‐ and Medium‐Sized Heterobiaryl Atropisomeric Rings and Atropopeptides by Catalytic Intramolecular S N Ar
inferred← citeshttps://doi.org/10.1002/anie.200800554openalex-snapshot
Synthesis of (−)‐Octalactin A by a Strategic Vanadium‐Catalyzed Oxidative Kinetic Resolution
inferred← citeshttps://doi.org/10.1002/anie.200804576openalex-snapshot
Intermolecular Double Prins‐Type Cyclization: A Facile and Efficient Synthesis of 1,6‐Dioxecanes
inferred← citeshttps://doi.org/10.1002/anie.201200425openalex-snapshot
Tandem Cross‐Dimerisation/Oxonia‐Cope Reaction of Carbonyl Compounds to Homoallylic Esters and Lactones
inferred← citeshttps://doi.org/10.1002/anie.201200450openalex-snapshot
Lewis Acid Catalyzed Intramolecular [4+2] and [3+2] Cross‐Cycloaddition of Alkynylcyclopropane Ketones with Carbonyl Compounds and Imines
inferred← citeshttps://doi.org/10.1002/anie.201200513openalex-snapshot
Synthesis of Eight‐Membered Lactones: Intermolecular [6+2] Cyclization of Amphoteric Molecules with Siloxy Alkynes
inferred← citeshttps://doi.org/10.1002/anie.201405834openalex-snapshot
Highly Enantioselective Rhodium(I)‐Catalyzed Carbonyl Carboacylations Initiated by CC Bond Activation
inferred← citeshttps://doi.org/10.1002/anie.201608198openalex-snapshot
Radical‐Mediated 1,2‐Formyl/Carbonyl Functionalization of Alkenes and Application to the Construction of Medium‐Sized Rings
inferred← citeshttps://doi.org/10.1002/anie.201608974openalex-snapshot
A Migratory Ether Formation Route to Medium‐Sized Sugar Mimetics
inferred← citeshttps://doi.org/10.1002/anie.201700113openalex-snapshot
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inferred← citeshttps://doi.org/10.1002/anie.201700596openalex-snapshot
Yttrium‐Catalyzed Intramolecular Hydroalkoxylation/Claisen Rearrangement Sequence: Efficient Synthesis of Medium‐Sized Lactams
inferred← citeshttps://doi.org/10.1002/anie.201809376openalex-snapshot
Gold‐Catalyzed Double Cycloisomerization of 1‐Ene‐4,10‐diynyl Esters to Bicyclo[6.3.0]undeca‐2,4,9‐trienyl Esters
inferred← citeshttps://doi.org/10.1002/anie.201810184openalex-snapshot
Enantioselective Organocatalytic Four‐Atom Ring Expansion of Cyclobutanones: Synthesis of Benzazocinones
inferred← citeshttps://doi.org/10.1002/anie.202012720openalex-snapshot
Photocatalytic Aerobic Oxidative Ring Expansion of Cyclic Ketones to Macrolactones by Cerium and Cyanoanthracene Catalysis
inferred← citeshttps://doi.org/10.1002/anie.202105882openalex-snapshot
Macrolactonization Reactions Driven by a Pentafluorobenzoyl Group**
inferred← citeshttps://doi.org/10.1002/anie.202206501openalex-snapshot
Atroposelective Construction of Nine‐Membered Carbonate‐Bridged Biaryls
inferred← citeshttps://doi.org/10.1002/anie.202213676openalex-snapshot
Palladium‐Catalyzed [6+2] Double Allene Annulation for Benzazocines Synthesis
inferred← citeshttps://doi.org/10.1002/anie.202300773openalex-snapshot
Tricrilactones A–H, Potent Antiosteoporosis Macrolides with Distinctive Ring Skeletons from Trichocladium crispatum, an Alpine Moss‐Associated Fungus
inferred← citeshttps://doi.org/10.1002/anie.202408195openalex-snapshot
Chromium‐ and Metal‐Reductant‐Free Asymmetric Nozaki–Hiyama–Kishi (NHK) Reaction Enabled by Metallaphotoredox Catalysis
inferred← citeshttps://doi.org/10.1002/anie.202416873openalex-snapshot
Catalytic Asymmetric Synthesis of Inherently Chiral Eight‐Membered O‐Heterocycles through Cross‐[4+4] Cycloaddition of Quinone Methides
inferred← citeshttps://doi.org/10.1002/anie.202525903openalex-snapshot
Homologative Radical 1,3‐Dicarbofunctionalization of Unactivated Alkenes Enabled by Sequential Functional Group Migrations
inferred← citeshttps://doi.org/10.1002/anie.8290035openalex-snapshot
Synthesis of Large‐ and Medium‐Sized Heterobiaryl Atropisomeric Rings and Atropopeptides by Catalytic Intramolecular S N Ar
inferred← citeshttps://doi.org/10.1002/asia.200700304openalex-snapshot
Total Synthesis of 2‐Hydroxytetracosanolide and 2‐Hydroxy‐24‐oxooctacosanolide By Using an Effective Lactonization
inferred← citeshttps://doi.org/10.1002/asia.200700305openalex-snapshot
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inferred← citeshttps://doi.org/10.1002/asia.70680openalex-snapshot
Ligand‐Controlled Divergent Synthesis of cis/trans ‐Trisubstituted Cycloalkenes via Pd‐Catalyzed [6+4] Cyclization
inferred← citeshttps://doi.org/10.1002/cbdv.201400058openalex-snapshot
A Novel Oxy‐Oxonia(Azonia)‐ Cope Reaction: Serendipitous Discovery and Its Application to the Synthesis of Macrocyclic Musks
inferred← citeshttps://doi.org/10.1002/cctc.201402967openalex-snapshot
Iron(II) Pincer‐Catalyzed Synthesis of Lactones and Lactams through a Versatile Dehydrogenative Domino Sequence
inferred← citeshttps://doi.org/10.1002/chem.200801548openalex-snapshot
A Highly Efficient Macrolactonization Method via Ethoxyvinyl Ester
inferred← citeshttps://doi.org/10.1002/chem.200900972openalex-snapshot
Highly Regio‐ and Stereoselective Synthesis of Nine‐ to Twelve‐Membered Cyclic Compounds by a Pd0‐Catalyzed Cyclization Reaction between Allenes with a Nucleophilic Functionality and Organic Halides
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Total Synthesis of the Bicyclic Depsipeptide HDAC Inhibitors Spiruchostatins A and B, 5′′‐epi‐Spiruchostatin B, FK228 (FR901228) and Preliminary Evaluation of Their Biological Activity
inferred← citeshttps://doi.org/10.1002/chem.200901735openalex-snapshot
Concise Enantioselective Synthesis of the Ten‐Membered Lactone Cephalosporolide G and Its C‐3 Epimer
inferred← citeshttps://doi.org/10.1002/chem.201103060openalex-snapshot
Asymmetric Synthesis of Densely Functionalized Medium‐Ring Carbocycles and Lactones through Modular Assembly and Ring‐Closing Metathesis of Sulfoximine‐Substituted Trienes and Dienynes
inferred← citeshttps://doi.org/10.1002/chem.201203667openalex-snapshot
Total Synthesis and Biological Evaluation of Grassypeptolide A
inferred← citeshttps://doi.org/10.1002/chem.201301785openalex-snapshot
Copper‐Catalyzed Direct Synthesis of Iodoenamides from Ketoximes
inferred← citeshttps://doi.org/10.1002/chem.201304297openalex-snapshot
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Domino Ring Expansion: Regioselective Access to 9‐Membered Lactones with a Fused Indole Unit from 2‐Nitrophenyl‐1,3‐cyclohexanediones
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inferred← citeshttps://doi.org/10.1002/chin.200722239openalex-snapshot
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inferred← citeshttps://doi.org/10.1002/cjoc.70120openalex-snapshot
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inferred← citeshttps://doi.org/10.1002/ejic.202200283openalex-snapshot
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inferred← citeshttps://doi.org/10.1002/ejoc.200800942openalex-snapshot
Kinetic Resolution of Racemic Carboxylic Acids Using Achiral Alcohols by the Promotion of Benzoic Anhydrides and Tetramisole Derivatives: Production of Chiral Nonsteroidal Anti‐Inflammatory Drugs and Their Esters
inferred← citeshttps://doi.org/10.1002/ejoc.201100368openalex-snapshot
Enzymatic Total Synthesis of Banana Volatile (S)‐2‐Pentyl (R)‐3‐Hydroxyhexanoate
inferred← citeshttps://doi.org/10.1002/ejoc.201300037openalex-snapshot
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inferred← citeshttps://doi.org/10.1002/ejoc.201301365openalex-snapshot
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inferred← citeshttps://doi.org/10.1002/ejoc.201500527openalex-snapshot
A Non‐Aldol Preparation of Enantiopure Propionate‐Derived Motifs with the Assistance of Chiral Sulfoxides: Application to a Convergent Synthesis of the Lactone Core of Octalactins
inferred← citeshttps://doi.org/10.1002/ejoc.201500654openalex-snapshot
Removable Silyl Group as a “Masked Proton” in Oxy‐2‐oxonia(azonia)‐Cope Rearrangement: Applications in Stereoselective Total Synthesis of Natural Macrolides
inferred← citeshttps://doi.org/10.1002/ejoc.201500894openalex-snapshot
Enantioselective Synthesis of Medium‐Sized‐Ring Lactones by Organocatalytic Michael Addition Followed by Reductively Initiated Fragmentation
inferred← citeshttps://doi.org/10.1002/ejoc.202100541openalex-snapshot
Iodine‐Catalyzed Construction of Dihydrooxepines via 3‐Methyl‐5‐Pyrazolones C−H Oxidation/Functionalization of Quinolines Cascade
inferred← citeshttps://doi.org/10.1002/ejoc.202200818openalex-snapshot
Steric Push towards the [n+3] Hydrated Imidazoline Ring Expansion (HIRE) of Dibenzo[1.4]oxazepines and Thiazepines
inferred← citeshttps://doi.org/10.1002/ejoc.202500331openalex-snapshot
Formal Higher‐Order [8 + 3] Cycloaddition of Azaheptafulvenes with Donor–Acceptor Cyclopropanes
inferred← citeshttps://doi.org/10.1002/ejoc.202500534openalex-snapshot
Selective Synthesis of Furan‐3(2H)‐one Fused Seven‐, Eight‐, or Nine‐Membered Ring from the Reaction of Diynone and Cyclic β‐Keto Ester
inferred← citeshttps://doi.org/10.1002/hlca.201000416openalex-snapshot
Asymmetric Total Synthesis of Stagonolide G
inferred← citeshttps://doi.org/10.1002/hlca.201100190openalex-snapshot
Stereoselective Total Synthesis of Stagonolide C
inferred← citeshttps://doi.org/10.1002/hlca.201200164openalex-snapshot
Stereoselective Total Synthesis of Multiplolide A and of a Diastereoisomer
inferred← citeshttps://doi.org/10.1002/hlca.201200434openalex-snapshot
Kinetic Resolution of Racemic Secondary Benzylic Alcohols by the Enantioselective Esterification Using Pyridine‐3‐carboxylic Anhydride (3‐PCA) with Chiral Acyl‐Transfer Catalysts
inferred← citeshttps://doi.org/10.1002/slct.201600350openalex-snapshot
RuCl 3 Promoted Efficient Synthesis of Z ‐Selective Macrocyclic Thiotetralactones via Ring‐Closing Metathesis
inferred← citeshttps://doi.org/10.1002/slct.201700921openalex-snapshot
Synthesis of (+)‐Patulolide C Using R ‐(+)‐γ‐Valerolactone as a Chiral Synthon.
inferred← citeshttps://doi.org/10.1002/slct.201900192openalex-snapshot
Total Synthesis of (+)‐Sacrolide A
inferred← citeshttps://doi.org/10.1002/slct.202100206openalex-snapshot
Applications of Yamaguchi Method to Esterification and Macrolactonization in Total Synthesis of Bioactive Natural Products
inferred← citeshttps://doi.org/10.1002/slct.202304288openalex-snapshot
Potassium tert ‐Butoxide‐Catalyzed Selective Synthesis of 1,4‐Benzodioxepines via 7‐exo/7‐endo‐dig Cyclization of Alkynol: Experimental and DFT Study
inferred← citeshttps://doi.org/10.1002/slct.202305002openalex-snapshot
Recent Progress in Transformations of Azepine/Oxazepine/Thiazepine Derivatives
inferred← citeshttps://doi.org/10.1002/tcr.200900017openalex-snapshot
Evaluation of the Efficiency of the Macrolactonization Using MNBA in the Synthesis of Erythromycin A Aglycon
inferred← citeshttps://doi.org/10.1002/tcr.201300022openalex-snapshot
Asymmetric M ukaiyama Aldol Reactions Using Chiral Diamine–Coordinated Sn (II) Triflate: Development and Application to Natural Product Synthesis
inferred← citeshttps://doi.org/10.1007/7081_2015_143openalex-snapshot
Metathetic Synthesis of Common and Medium-Sized Lactones: The State of the Art
inferred← citeshttps://doi.org/10.1007/978-3-642-41470-1_2openalex-snapshot
Synthesis of Eight- to Ten-Membered Ring Ethers
inferred← citeshttps://doi.org/10.1007/s11172-020-2965-6openalex-snapshot
New syntheses of haloketo acid methyl esters and their transformation to halolactones by reductive cyclization
inferred← citeshttps://doi.org/10.1007/s11426-021-1135-8openalex-snapshot
Steric-switched defluorofunctionalization selectivity: controlled synthesis of monofluoroalkene-masked medium-sized heterocyclic lactams and lactones
inferred← citeshttps://doi.org/10.1007/s11426-022-1283-7openalex-snapshot
Oxidative lactonization of C(sp3)-H bond in methyl aromatic alcohols enabled by proton-coupled electron transfer
inferred← citeshttps://doi.org/10.1007/s11426-022-1374-4openalex-snapshot
Construction of enantioenriched eight-membered lactones via Pd-catalyzed asymmetric (6+2) dipolar annulation
inferred← citeshttps://doi.org/10.1007/s11426-023-1622-1openalex-snapshot
Synthesis of medium-sized benzo[b]azocines and benzo[b]azonines by photoinduced 8-/9-endo sulfonyl-cyclization
inferred← citeshttps://doi.org/10.1016/b978-0-08-097774-4.00614-8openalex-snapshot
Asymmetric Epoxidation and Sulfoxidation
inferred← citeshttps://doi.org/10.1016/b978-0-12-385464-3.00001-7openalex-snapshot
The Literature of Heterocyclic Chemistry, Part X, 2005–2007
inferred← citeshttps://doi.org/10.1016/b978-0-12-386540-3.00001-0openalex-snapshot
Total Syntheses of Solandelactones E and F
inferred← citeshttps://doi.org/10.1016/b978-0-12-800070-0.00011-6openalex-snapshot
Green Synthetic Approaches for Medium Ring-Sized Heterocycles of Biological Interest
inferred← citeshttps://doi.org/10.1016/b978-0-323-95652-9.00003-xopenalex-snapshot
Synthesis of diazocines and oxocines by cyclization of dienes
inferred← citeshttps://doi.org/10.1016/b978-0-323-95652-9.00018-1openalex-snapshot
Synthesis of azocines and oxocines by ring closure of halo, amine, and oxo compounds
inferred← citeshttps://doi.org/10.1016/j.bioorg.2026.109768openalex-snapshot
Discovery of novel ten-membered lactones as osteoblastogenesis agents targeting Wnt/β-catenin signaling pathway
inferred← citeshttps://doi.org/10.1016/j.bmc.2012.03.036openalex-snapshot
Structure–activity relationships and key structural feature of pyridyloxybenzene-acylsulfonamides as new, potent, and selective peroxisome proliferator-activated receptor (PPAR) γ Agonists
inferred← citeshttps://doi.org/10.1016/j.bmc.2022.116820openalex-snapshot
Design and synthesis of unprecedented 9- and 10-membered cyclonucleosides with PRMT5 inhibitory activity
inferred← citeshttps://doi.org/10.1016/j.bmcl.2011.06.026openalex-snapshot
Synthesis and cytotoxicity of the depsipeptides analogues of callipeltin B
inferred← citeshttps://doi.org/10.1016/j.carres.2011.04.017openalex-snapshot
Polymer-mediated cyclodehydration of alditols and ketohexoses
inferred← citeshttps://doi.org/10.1016/j.cclet.2015.07.006openalex-snapshot
A novel synthetic route to rac -( Z )-recifeiolide from cyclooctanone and acetaldehyde
inferred← citeshttps://doi.org/10.1016/j.cclet.2023.109058openalex-snapshot
Chemoselective electrochemical seleno-cyclization of dienes to medium-sized benzo[b]azocines
inferred← citeshttps://doi.org/10.1016/j.checat.2022.07.021openalex-snapshot
Recent advances for the catalytic asymmetric construction of medium-sized rings
inferred← citeshttps://doi.org/10.1016/j.ejmech.2012.12.023openalex-snapshot
Total synthesis of bicyclic depsipeptides spiruchostatins C and D and investigation of their histone deacetylase inhibitory and antiproliferative activities
inferred← citeshttps://doi.org/10.1016/j.ejmech.2014.02.044openalex-snapshot
Total synthesis of burkholdacs A and B and 5,6,20-tri-epi-burkholdac A: HDAC inhibition and antiproliferative activity
inferred← citeshttps://doi.org/10.1016/j.ejmech.2016.05.031openalex-snapshot
Synthesis and biological evaluation of novel FK228 analogues as potential isoform selective HDAC inhibitors
inferred← citeshttps://doi.org/10.1016/j.jinorgbio.2017.12.004openalex-snapshot
Synthesis and evaluation of the antibiotic and adjuvant antibiotic potential of organotin(IV) derivatives
inferred← citeshttps://doi.org/10.1016/j.jorganchem.2017.09.044openalex-snapshot
Nitroaldol reaction catalyzed by arylhydrazone di- and triorganotin(IV) complexes
inferred← citeshttps://doi.org/10.1016/j.jorganchem.2020.121629openalex-snapshot
Oxazolidinones as chiral auxiliaries in asymmetric aldol reaction applied to natural products total synthesis
inferred← citeshttps://doi.org/10.1016/j.molcata.2015.02.010openalex-snapshot
Selectivity controlled by ligand tuning in the palladium-catalysed cyclocarbonylation: Synthesis of new γ and δ lactones from a natural sesquiterpene
inferred← citeshttps://doi.org/10.1016/j.molstruc.2026.147631openalex-snapshot
Tri-/di-/mono-fluoroalkylation cyclization: Access to fluoroalkyl functionalized indole fused medium-sized N-heterocycles
inferred← citeshttps://doi.org/10.1016/j.tet.2007.09.009openalex-snapshot
Synthesis of benzo-fused medium ring cyclic ethers via a Michael addition–ring closing metathesis strategy involving nitroaliphatic compounds
inferred← citeshttps://doi.org/10.1016/j.tet.2007.09.080openalex-snapshot
Stereoselective synthesis of the bacterial DNA primase inhibitor Sch 642305 and its C-4 epimer
inferred← citeshttps://doi.org/10.1016/j.tet.2008.04.026openalex-snapshot
Synthetic efforts toward the synthesis of octalactins
inferred← citeshttps://doi.org/10.1016/j.tet.2012.05.081openalex-snapshot
Recent progress in the synthesis of oxepanes and medium ring ethers
inferred← citeshttps://doi.org/10.1016/j.tet.2013.07.064openalex-snapshot
Silver carboxylate promoted lactonization: a general method applicable to prepare medium and large-sized lactones without high dilution or slow addition
inferred← citeshttps://doi.org/10.1016/j.tet.2013.07.083openalex-snapshot
Total synthesis of (+)-azimine via diastereoselective aminopalladation
inferred← citeshttps://doi.org/10.1016/j.tet.2013.09.056openalex-snapshot
Synthesis of fused nine-membered rings: a simple protocol for synthesis of [1,2,3]-triazolo-[1,4]-benzoxazonine frameworks from the Baylis–Hillman acetates
inferred← citeshttps://doi.org/10.1016/j.tet.2019.06.015openalex-snapshot
Divergent total synthesis of aspinolides B, E and J
inferred← citeshttps://doi.org/10.1016/j.tet.2020.131163openalex-snapshot
Synthesis of medium-sized lactones from siloxy alkynes via ring expansion
inferred← citeshttps://doi.org/10.1016/j.tet.2021.132141openalex-snapshot
Total synthesis of LC-KA05, the proposed structure of LC-KA05-2, and 2,18-seco-lankacidinol B: A quest to revisit lankacidin biosynthesis
inferred← citeshttps://doi.org/10.1016/j.tet.2025.134954openalex-snapshot
NHC-catalyzed higher-order (5 + 3) cyclization for accessing tetracyclic eight-membered lactones
inferred← citeshttps://doi.org/10.1016/j.tetasy.2009.10.007openalex-snapshot
Chemo-enzymatic asymmetric total synthesis of stagonolide-C
inferred← citeshttps://doi.org/10.1016/j.tetasy.2012.10.007openalex-snapshot
Asymmetric synthesis of (+)-stagonolide C and (−)-aspinolide A via organocatalysis
inferred← citeshttps://doi.org/10.1016/j.tetasy.2016.05.008openalex-snapshot
Stereoselective synthesis of (R)-(−) and (S)-(+)-phoracantholide I from (R)-(+)-γ-valerolactone
inferred← citeshttps://doi.org/10.1016/j.tetlet.2007.09.135openalex-snapshot
The first asymmetric esterification of free carboxylic acids with racemic alcohols using benzoic anhydrides and tetramisole derivatives: an application to the kinetic resolution of secondary benzylic alcohols
inferred← citeshttps://doi.org/10.1016/j.tetlet.2010.01.082openalex-snapshot
Stereoselective synthesis (+)-cephalosporolide D
inferred← citeshttps://doi.org/10.1016/j.tetlet.2010.05.079openalex-snapshot
A concise stereoselective total synthesis of Botryolide B
inferred← citeshttps://doi.org/10.1016/j.tetlet.2010.11.136openalex-snapshot
Expected and unexpected reactions of 1,3-benzothiazine derivatives, II. Formation of isomeric 5,6-dihydro-1,5-benzothiazocines
inferred← citeshttps://doi.org/10.1016/j.tetlet.2011.11.059openalex-snapshot
Chemoenzymatic total synthesis of stagonolide-E
inferred← citeshttps://doi.org/10.1016/j.tetlet.2014.05.016openalex-snapshot
Cu-promoted single-pot intramolecular esterification of C-3 functionalized azetidin-2-one: an efficient diastereoselective access to azido-/amino-aza-lactones
inferred← citeshttps://doi.org/10.1016/j.tetlet.2015.01.181openalex-snapshot
Total synthesis of (3R,16E,20E,23R)-(−)-eushearilide and structural determination of naturally occurring eushearilide
inferred← citeshttps://doi.org/10.1016/j.tetlet.2015.09.082openalex-snapshot
An efficient organocatalytic route for asymmetric total synthesis of Stagonolide F
inferred← citeshttps://doi.org/10.1016/j.tetlet.2018.11.044openalex-snapshot
Antiviral drug nevirapine as a template for hydrated imidazoline ring expansion (HIRE): Rapid access to the diarene-fused 1,4,7-triazecine ring system
inferred← citeshttps://doi.org/10.1016/j.tetlet.2021.153567openalex-snapshot
Electrochemical oxidative bromolactonization of unsaturated carboxylic acids with sodium bromide: Synthesis of bromomethylated γ-lactones
inferred← citeshttps://doi.org/10.1016/j.tetlet.2022.153718openalex-snapshot
Heteroatom is not needed: Access to dibenzo[e,h][1,4]diazecin-9-ones from dibenzo[b,e]azepin-6-one via the hydrated imidazoline ring expansion (HIRE) approach
inferred← citeshttps://doi.org/10.1021/acs.chemrev.0c00793openalex-snapshot
Construction of Medium-Sized Rings by Gold Catalysis
inferred← citeshttps://doi.org/10.1021/acs.jnatprod.7b00368openalex-snapshot
Asymmetric Total Synthesis of (−)-Astakolactin and Confirmation of Its Stereostructure
inferred← citeshttps://doi.org/10.1021/acs.joc.1c00236openalex-snapshot
Sulfur Oxidation Increases the Rate of HIRE-Type [1.4]Thiazepinone Ring Expansion and Influences the Conformation of a Medium-Sized Heterocyclic Scaffold
inferred← citeshttps://doi.org/10.1021/acs.joc.3c01114openalex-snapshot
Gold and Palladium Relay Catalytic [4 + 4] Cycloadditions of Enynamides and γ-Methylene-δ-valerolactones: Diastereoselective Construction of Furan-Fused Azacyclooctanes
inferred← citeshttps://doi.org/10.1021/acs.joc.3c02931openalex-snapshot
Cascade Electrochemical Aerobic Oxygenation of 2-Substituted Indoles and Electrochemical [5 + 3] Annulation with Amidines: Access to Eight-Membered Benzo[1,3,5]triazocin-6(5H)-ones
inferred← citeshttps://doi.org/10.1021/acs.joc.4c01935openalex-snapshot
Base-Controlled Synthesis of Heteroatom-Embedded 9-Membered Cycloalkynes and 6-Membered Sultams through Copper-Catalyzed Cyclization
inferred← citeshttps://doi.org/10.1021/acs.joc.4c02278openalex-snapshot
Access to Functionalized Amines and Medium N-Heterocycles via Amine-Enabled Remote C–H Alkynylation
inferred← citeshttps://doi.org/10.1021/acs.joc.4c02657openalex-snapshot
Sc(OTf)3-Catalyzed Precise Construction of Medium-Sized [4.2.1]-Oxabridged Scaffolds
inferred← citeshttps://doi.org/10.1021/acs.joc.4c03187openalex-snapshot
Visible-Light-Induced Sulfonylation Cyclization to Generate Indole-Fused Medium-Sized N-Heterocycles in 2-Me-THF
inferred← citeshttps://doi.org/10.1021/acs.joc.5c00479openalex-snapshot
Inherently Chiral Seven- and Eight-Membered Rings: Enantioselective Synthesis and Applications
inferred← citeshttps://doi.org/10.1021/acs.joc.5c02501openalex-snapshot
Construction of Bridged N,O -Heterocycles via Palladium-Catalyzed [5 + 4] Cycloadditions of Azabicyclo[2.1.0]pentanes and Vinyl Oxiranes
inferred← citeshttps://doi.org/10.1021/acs.joc.7b01973openalex-snapshot
Formal Total Synthesis of Amphidinolide E
inferred← citeshttps://doi.org/10.1021/acs.joc.7b02628openalex-snapshot
Direct Decarboxylative–Decarbonylative Alkylation of α-Oxo Acids with Electrophilic Olefins via Visible-Light Photoredox Catalysis
inferred← citeshttps://doi.org/10.1021/acs.joc.8b00774openalex-snapshot
Total Synthesis and Antimicrobial Activities of All Stereoisomers of (16Z,20E)-Eushearilide and (16E,20E)-Eushearilide
inferred← citeshttps://doi.org/10.1021/acs.joc.8b01210openalex-snapshot
Rare Medium-Sized Rings Prepared via Hydrolytic Imidazoline Ring Expansion (HIRE)
inferred← citeshttps://doi.org/10.1021/acs.joc.8b02465openalex-snapshot
Configuration-Dependent Medium-Sized Ring Formation: Chiral Molecular Framework with Three-Dimensional Architecture
inferred← citeshttps://doi.org/10.1021/acs.joc.8b02805openalex-snapshot
Rethinking Hydrolytic Imidazoline Ring Expansion: A Common Approach to the Preparation of Medium-Sized Rings via Side-Chain Insertion into [1.4]Oxa- and [1.4]Thiazepinone Scaffolds
inferred← citeshttps://doi.org/10.1021/acs.joc.9b00870openalex-snapshot
Synthesis of 23-, 25-, 27-, and 29-Membered (Z)-Selective Unsaturated and Saturated Macrocyclic Lactones from 16- and 17-Membered Macrocyclic Lactones and Bromoalcohols by Wittig Reaction, Yamaguchi Macrolactonization, and Photoinduced Decarboxylative Radical Macrolactonization
inferred← citeshttps://doi.org/10.1021/acs.joc.9b01269openalex-snapshot
Highly Substituted Medium-Sized Ring-Fused Azocinoquinoline Scaffolds by Post-Ugi-4CR Reductive Carbopalladation Cyclization
inferred← citeshttps://doi.org/10.1021/acs.joc.9b03516openalex-snapshot
Total Synthesis and Antimicrobial Activity of Tumescenamide C and Its Derivatives
inferred← citeshttps://doi.org/10.1021/acs.orglett.0c01391openalex-snapshot
Visible-Light-Induced Dehydrohalogenative Coupling for Intramolecular α-Alkenylation: A Way to Build Seven- and Eight-Membered Rings
inferred← citeshttps://doi.org/10.1021/acs.orglett.1c00183openalex-snapshot
Pd-catalyzed Regio- and Stereoselective Hydrostannylation of an Alkyl Ethynyl Ether/One-Pot Stille Coupling Enables the Synthesis of 14-Membered Macrolactone of Luminamicin
inferred← citeshttps://doi.org/10.1021/acs.orglett.1c01770openalex-snapshot
Designing and Accurately Developing a [6 + 2] Dipolar Cycloaddition for the Synthesis of Benzodiazocines
inferred← citeshttps://doi.org/10.1021/acs.orglett.1c02506openalex-snapshot
Identification and Total Synthesis of an Unstable Anticancer Macrolide Presaccharothriolide Z Produced by Saccharothrix sp. A1506
inferred← citeshttps://doi.org/10.1021/acs.orglett.1c02702openalex-snapshot
Benzyne-Mediated Esterification Reaction
inferred← citeshttps://doi.org/10.1021/acs.orglett.1c04340openalex-snapshot
Total Syntheses of Strasseriolide A and B, Antimalarial Macrolide Natural Products
inferred← citeshttps://doi.org/10.1021/acs.orglett.2c04284openalex-snapshot
Organophosphorus-Catalyzed Borylative Ring-Opening of Vinylcyclopropanes: A Stereoselective Route to δ-Valerolactones
inferred← citeshttps://doi.org/10.1021/acs.orglett.3c01714openalex-snapshot
Cascade Radical Trifluoromethylthiolation/Cyclization of Dienes To Access SCF3-Containing Medium-Sized Heterocycles
inferred← citeshttps://doi.org/10.1021/acs.orglett.3c03913openalex-snapshot
Ruthenium-Catalyzed Carbonylation of α-Aminoaryl-Tethered Alkylidenecyclopropanes: Synthesis of Eight-Membered Benzolactams
inferred← citeshttps://doi.org/10.1021/acs.orglett.3c04014openalex-snapshot
Accessing Medium-Sized Rings via Vinyl Carbocation Intermediates
inferred← citeshttps://doi.org/10.1021/acs.orglett.4c02345openalex-snapshot
Bridged Biaryl Atropisomers by Organocatalyzed Kinetic Asymmetric Alcoholysis
inferred← citeshttps://doi.org/10.1021/acs.orglett.4c03619openalex-snapshot
Rh(II)-Catalyzed Selective C(sp3)–H/C(sp2)–H Bonds Cascade Insertion to Construct [6–8–6] Benzo-Fused Scaffold
inferred← citeshttps://doi.org/10.1021/acs.orglett.4c04632openalex-snapshot
Photoinduced Difluoromethylation Cyclization to Generate Medium-Sized Difluoro-benzo[b]azepines
inferred← citeshttps://doi.org/10.1021/acs.orglett.4c04715openalex-snapshot
Visible-Light-Induced [4 + 3]-Annulation of Carbonyl Ylides with Alkenyl Pyrazolinone for Constructing [4.2.1]-Oxo-Bridged Oxocine Skeleton
inferred← citeshttps://doi.org/10.1021/acs.orglett.5c02371openalex-snapshot
Construction of Eight-Membered N -Heterocycles via Palladium-Catalyzed Cyclization of Allenyl Isocyanides
inferred← citeshttps://doi.org/10.1021/acs.orglett.5c04153openalex-snapshot
A Synthetic Approach to Diverse Indole/Oxindole-Annulated S -Heterocycles
inferred← citeshttps://doi.org/10.1021/acs.orglett.6c01548openalex-snapshot
Lewis-Acid-Catalyzed Cyclization of Bicyclo[1.1.0]butanes with Alkenyl Cyclic Dithioacetals for the Synthesis of 11-Membered Bicyclic Medium-Sized Rings
inferred← citeshttps://doi.org/10.1021/acs.orglett.6c02076openalex-snapshot
A Dearomative Domino Approach for Stereoselective Construction of Functionalized Bridged [4.3.1] Bicycles
inferred← citeshttps://doi.org/10.1021/acs.orglett.6c02782openalex-snapshot
Photoredox-Enabled Chemo-Selective Construction of Indole-Fused Medium-Sized Difluoro-diazocines
inferred← citeshttps://doi.org/10.1021/acs.orglett.7b02688openalex-snapshot
Nucleo-Palladation-Triggering Alkene Functionalization: A Route to γ-Lactones
inferred← citeshttps://doi.org/10.1021/acs.orglett.8b01720openalex-snapshot
Dearomatization of Indole via Intramolecular [3 + 2] Cycloaddition: Access to the Pentacyclic Skeleton of Strychons Alkaloids
inferred← citeshttps://doi.org/10.1021/acs.orglett.8b03327openalex-snapshot
Stereoselective Synthesis of Diverse Lactones through a Cascade Reaction of Rhodium Carbenoids with Ketoacids
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