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Polymerization with the Cu( <scp>i</scp> )-catalyzed Doyle–Kirmse reaction of bis(allyl sulfides) and bis(α-diazoesters)
45/45 checkable references clean · checked 2026-08-19
Every reference with a DOI in the deposited reference list resolved to a known work in Crossref or DataCite at the dated check, and none carried a retraction, withdrawal, or removal notice.
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The 45 checked references that resolve
resolves10.1016/j.polymer.2018.11.049
Polymerization of diazoacetates: New synthetic strategy for C-C main chain polymers
resolves10.1021/jacs.8b11628
Fast Living Polymerization and Helix-Sense-Selective Polymerization of Diazoacetates Using Air-Stable Palladium(II) Catalysts
resolves10.1021/acs.macromol.9b01682
Highly Enantioselective and Helix-Sense-Controlled Synthesis of Stereoregular Helical Polycarbenes Using Chiral Palladium(II) Catalysts
resolves10.1021/acs.macromol.9b00653
Poly(β-keto enol ether) Prepared by Three-Component Polycondensation of Bis(diazoketone), Bis(1,3-diketone), and Tetrahydrofuran: Mild Acid-Degradable Polymers To Afford Well-Defined Low Molecular Weight Components
resolves10.1039/D0PY00185F
Polycondensation of bis(α-diazo-1,3-dicarbonyl) compounds with dicarboxylic acids: an efficient access to functionalized alternating polyesters
resolves10.1021/acs.macromol.1c01966
Cp(π-Allyl)Pd-Initiated Polymerization of Diazoacetates: Reaction Development, Kinetic Study, and Chain Transfer with Alcohols
resolves10.1021/ma100494a
Polycondensation of Bis(diazocarbonyl) Compounds with Aromatic Diols and Cyclic Ethers: Synthesis of New Type of Polyetherketones
resolves10.1021/ma201037p
Three-Component Polycondensation of Bis(diazoketone) with Dicarboxylic Acids and Cyclic Ethers: Synthesis of New Types of Poly(ester ether ketone)s
resolves10.1021/acs.macromol.7b01994
Ru-Catalyzed Polycondensation of Dialkyl 1,4-Phenylenebis(diazoacetate) with Dianiline: Synthesis of Well-Defined Aromatic Polyamines Bearing an Alkoxycarbonyl Group at the Adjacent Carbon of Each Nitrogen in the Main Chain Framework
resolves10.1039/c3nj00339f
Denitrogen alkene polymerization of bisdiazo compounds by copper(ii) catalysts
resolves10.1021/ma401047x
Synthesis of Well-Defined Unsaturated Polyesters by Transition-Metal-Catalyzed Polycondensation of Bis(diazoacetate)s
resolves10.1021/acsomega.9b03408
Single-Component Polycondensation of Bis(alkoxycarbonyldiazomethyl)aromatic
Compounds To Afford Poly(arylene vinylene)s with an Alkoxycarbonyl
Group on Each Vinylene Carbon Atom
resolves10.1021/acs.macromol.8b02163
Palladium-Catalyzed Cross-Coupling Polymerization: A New Access to Cross-Conjugated Polymers with Modifiable Structure and Tunable Optical/Conductive Properties
resolves10.1039/C8PY01529E
Palladium-catalyzed carbene coupling of
<i>N</i>
-tosylhydrazones and arylbromides to synthesize cross-conjugated polymers
resolves10.1039/b000708k
Catalytic enantioselective rearrangements and cycloadditions involving ylides from diazo compounds
resolves10.1016/j.ccr.2009.12.005
Catalytic [2,3]-sigmatropic rearrangement of sulfur ylide derived from metal carbene
resolves10.1016/j.tet.2016.11.045
Transition metal-catalyzed [2,3]-sigmatropic rearrangements of ylides: An update of the most recent advances
resolves10.1002/cber.19681010333
Reaktionen des Diazomethans mit Diallylsulfid und Allyläthern unter Kupfersalz‐Katalyse
resolves10.1021/jo00338a008
Highly effective catalytic methods for ylide generation from diazo compounds. Mechanism of the rhodium- and copper-catalyzed reactions with allylic compounds
resolves10.1021/ja055021d
Highly Stereoselective [2,3]-Sigmatropic Rearrangement of Sulfur Ylide Generated through Cu(I) Carbene and Sulfides
resolves10.1038/nchem.2789
Catalytic asymmetric trifluoromethylthiolation via enantioselective [2,3]-sigmatropic rearrangement of sulfonium ylides
resolves10.1021/jacs.7b12486
Chiral Nickel(II) Complex Catalyzed Enantioselective Doyle–Kirmse Reaction of α-Diazo Pyrazoleamides
resolves10.1039/D1PY01065D
The synthesis of degradable sulfur-containing polymers: precise control of structure and stereochemistry
resolves10.1038/nchem.1624
The use of elemental sulfur as an alternative feedstock for polymeric materials
resolves10.1021/acs.macromol.7b01788
Polythioamides of High Refractive Index by Direct Polymerization of Aliphatic Primary Diamines in the Presence of Elemental Sulfur
resolves10.1021/jacs.8b02886
Room Temperature One-Step Conversion from Elemental Sulfur to Functional Polythioureas through Catalyst-Free Multicomponent Polymerizations
resolves10.1021/jacs.9b11066
Economic Sulfur Conversion to Functional Polythioamides through Catalyst-Free Multicomponent Polymerizations of Sulfur, Acids, and Amines
resolves10.1021/jacs.1c00243
Sulfur Conversion to Multifunctional Poly(<i>O</i>-thiocarbamate)s through Multicomponent Polymerizations of Sulfur, Diols, and Diisocyanides
resolves10.1021/jacs.9b00031
4-Hydroxyproline-Derived Sustainable Polythioesters: Controlled Ring-Opening Polymerization, Complete Recyclability, and Facile Functionalization
resolves10.1021/ja8026168
Allyl Sulfides Are Privileged Substrates in Aqueous Cross-Metathesis: Application to Site-Selective Protein Modification
resolves10.1039/C8SC02877J
Cyclic tris-[5]helicenes with single and triple twisted Möbius topologies and Möbius aromaticity
resolves10.1021/jm000148t
Synthesis and Structure−Activity Relationships of 7-Substituted 3-(2,6-Dichlorophenyl)-1,6-naphthyridin-2(1<i>H</i>)-ones as Selective Inhibitors of pp60<i><sup>c</sup></i><sup>-<i>src</i></sup>
resolves10.1002/anie.201707092
Enantioselective [2,3]‐Sigmatropic Rearrangements: Metal‐Bound or Free Ylides as Reaction Intermediates?
resolves10.1021/acscatal.0c04768
Metal Bound or Free Ylides as Reaction Intermediates in Metal-Catalyzed [2,3]-Sigmatropic Rearrangements? It Depends
resolves10.1021/acscatal.0c04620
Mechanistic Studies of Copper(I)-Catalyzed Stereoselective [2,3]-Sigmatropic Rearrangements of Diazoesters with Allylic Iodides/Sulfides
The 2 references without a DOI — listed, not checked
no DOI — not checkedM. P.Doyle , M. A.McKervey and T.Ye , Modern Catalytic Methods for Organic Synthesis with Diazo Compounds , Wiley , New York , 1998
no DOI — not checkedD2PY00162D/cit19/1
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