Reference health
Blue light-promoted photolysis of aryldiazoacetates
71/71 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.
2 without a DOI — not checked. A reference deposited without a DOI is never matched by title or guessed at; it stays outside the checked set, and this line discloses that.
The 71 checked references that resolve
resolves10.1039/c0cs00217h
Guiding principles for site selective and stereoselective intermolecular C–H functionalization by donor/acceptor rhodium carbenes
resolves10.1039/b901170f
Application of donor/acceptor-carbenoids to the synthesis of natural products
resolves10.1021/ja069314y
Enhancement of Cyclopropanation Chemistry in the Silver-Catalyzed Reactions of Aryldiazoacetates
resolves10.1002/chem.201403283
Urea‐Induced Acid Amplification: A New Approach for Metal‐Free Insertion Chemistry
resolves10.1021/ol102923h
Nonmetal Catalyzed Insertion Reactions of Diazocarbonyls to Acid Derivatives in Fluorinated Alcohols
resolves10.1055/s-0035-1561061
Divergent Roles of Urea and Phosphoric Acid Derived Catalysts in Reactions of Diazo Compounds
resolves10.1021/jacs.6b00278
Copper-Catalyzed Oxy-Alkynylation of Diazo Compounds with Hypervalent Iodine Reagents
resolves10.1021/ja3031054
Urea Activation of α-Nitrodiazoesters: An Organocatalytic Approach to N–H Insertion Reactions
resolves10.1039/B207389G
Catalytic insertion of diazo compounds into N–H bonds: the copper alternative
resolves10.1021/ol800087p
Ruthenium-Catalyzed One-Pot Carbenoid N−H Insertion Reactions and Diastereoselective Synthesis of Prolines
resolves10.1021/ja503163k
Highly Site-Selective Direct C–H Bond Functionalization of Phenols with α-Aryl-α-diazoacetates and Diazooxindoles via Gold Catalysis
resolves10.1021/acs.orglett.7b03390
Gold-Catalyzed Controllable C2-Functionalization of Benzofurans with Aryl Diazoesters
resolves10.1021/ja305771y
Rh-Catalyzed Intermolecular Carbenoid Functionalization of Aromatic C–H Bonds by α-Diazomalonates
resolves10.1039/C5CC05000F
Pd(
<scp>ii</scp>
)-catalyzed formal [4+1] cycloaddition reactions of diazoacetates and aryl propargyl alcohols to form 2,5-dihydrofurans
resolves10.1002/anie.201606139
Gold‐Catalyzed Formal [4+1]/[4+3] Cycloadditions of Diazo Esters with Triazines
resolves10.1002/anie.201100134
One‐Step Catalytic Asymmetric Synthesis of Configurationally Stable Tröger Bases
resolves10.1002/adsc.201701069
Palladium‐Catalyzed [5+1] Annulation of 2‐(1‐Arylvinyl) Anilines and α‐Diazocarbonyl Compounds toward Multi‐functionalized Quinolines
resolves10.1021/acs.orglett.7b02436
Rhodium- and Non-Metal-Catalyzed Approaches for the Conversion of Isoxazol-5-ones to 2,3-Dihydro-6
<i>H</i>
-1,3-oxazin-6-ones
resolves10.1002/anie.201705202
A Stereoselective [3+1] Ring Expansion for the Synthesis of Highly Substituted Methylene Azetidines
resolves10.1039/c0sc00109k
Solvent-free catalytic enantioselective C–C bond forming reactions with very high catalyst turnover numbers
resolves10.1002/anie.201202512
Screening Rhodium Metallopeptide Libraries “On Bead”: Asymmetric Cyclopropanation and a Solution to the Enantiomer Problem
resolves10.1002/chem.201504817
Design and Synthesis of Novel Chiral Dirhodium(II) Carboxylate Complexes for Asymmetric Cyclopropanation Reactions
resolves10.1021/ja2074104
<i>D</i><sub>2</sub>-Symmetric Dirhodium Catalyst Derived from a 1,2,2-Triarylcyclopropanecarboxylate Ligand: Design, Synthesis and Application
resolves10.1002/anie.201406853
Enantioselective Iron‐Catalyzed Intramolecular Cyclopropanation Reactions
resolves10.1021/jacs.7b03086
Highly Enantioselective Copper- and Iron-Catalyzed Intramolecular Cyclopropanation of Indoles
resolves10.1021/acscatal.6b02184
Asymmetric Catalytic Insertion of α-Diazo Carbonyl Compounds into O–H Bonds of Carboxylic Acids
resolves10.1002/adsc.201700572
Rhodium(II)/Chiral Phosphoric Acid‐Cocatalyzed Enantioselective O–H Bond Insertion of α‐Diazo Esters
resolves10.1021/ja2084493
Well-Defined Binuclear Chiral Spiro Copper Catalysts for Enantioselective N–H Insertion
resolves10.1002/anie.201001686
Highly Enantioselective Insertion of Carbenoids into NH Bonds Catalyzed by Copper(I) Complexes of Binol Derivatives
resolves10.1002/anie.201611845
Enantioselective Palladium‐Catalyzed Carbene Insertion into the N−H Bonds of Aromatic Heterocycles
resolves10.1002/anie.201105485
Asymmetric NH Insertion Reaction Cooperatively Catalyzed by Rhodium and Chiral Spiro Phosphoric Acids
resolves10.1021/ja074483j
Copper-Catalyzed Asymmetric N−H Insertion Reactions: Couplings of Diazo Compounds with Carbamates to Generate α-Amino Acids
resolves10.1038/nature17651
Site-selective and stereoselective functionalization of unactivated C–H bonds
resolves10.1038/nature24641
Site-selective and stereoselective functionalization of non-activated tertiary C–H bonds
resolves10.1021/ja504797x
Role of Sterically Demanding Chiral Dirhodium Catalysts in Site-Selective C–H Functionalization of Activated Primary C–H Bonds
resolves10.1021/acs.orglett.6b02192
Highly Regio- and Enantioselective Formal [3 + 2]-Annulation of Indoles with Electrophilic Enol Carbene Intermediates
resolves10.1021/ja4069003
Rh
<sub>2</sub>
(
<i>R</i>
-TPCP)
<sub>4</sub>
-Catalyzed Enantioselective [3+2]-Cycloaddition between Nitrones and Vinyldiazoacetates
resolves10.1039/b000708k
Catalytic enantioselective rearrangements and cycloadditions involving ylides from diazo compounds
resolves10.1038/nchem.2789
Catalytic asymmetric trifluoromethylthiolation via enantioselective [2,3]-sigmatropic rearrangement of sulfonium ylides
resolves10.1070/RCR4519
Photochemical transformations of diazocarbonyl compounds: expected and novel reactions
resolves10.1021/ja1050023
Enantiomerically Pure
<i>trans</i>
-β-Lactams from α-Amino Acids via Compact Fluorescent Light (CFL) Continuous-Flow Photolysis
resolves10.1039/C4RA15670F
LED lighting as a simple, inexpensive, and sustainable alternative for Wolff rearrangements
resolves10.1021/ol501933h
Metal-Free Visible-Light Induced Cross-Dehydrogenative Coupling of Tertiary Amines with Diazo Compounds
resolves10.1038/ncomms4155
Diversity-oriented synthesis as a tool for identifying new modulators of mitosis
resolves10.1021/jo00229a006
Wavelength-dependent photochemistry of a diazo compound. Irradiation of 9-diazo-1,8-diazafluorene with ultraviolet or visible light
resolves10.1039/P29800000603
The reactivity of carbenes from photolysis of diazo-compounds towards carbon–hydrogen bonds. Effects of structure, temperature, and matrix on the insertion selectivity
resolves10.1002/hlca.19720550804
Die Photochemie von Diazo‐dibenzoylmethan Eine wellenlängen‐ und temperaturabhängige Photoreaktion
resolves10.1021/acs.orglett.8b00427
Harnessing the β-Silicon Effect for Regioselective and Stereoselective Rhodium(II)-Catalyzed C–H Functionalization by Donor/Acceptor Carbenes Derived from 1-Sulfonyl-1,2,3-triazoles
resolves10.1002/anie.200702131
Mechanism of Methyl Esterification of Carboxylic Acids by Trimethylsilyldiazomethane
resolves10.1021/ol702218w
Balance between Allylic C−H Activation and Cyclopropanation in the Reactions of Donor/Acceptor-Substituted Rhodium Carbenoids with <i>trans</i>-Alkenes
resolves10.1021/jo01331a023
Photolysis of N,N-diethyldiazoacetamide. Participation of a noncarbenic process in intramolecular carbon-hydrogen insertion
resolves10.1021/ja983277w
Reversible Interconversion between Singlet and Triplet 2-Naphthyl(carbomethoxy)carbene
resolves10.1021/ja983278o
Time-Resolved IR Studies of 2-Naphthyl(carbomethoxy)carbene: Reactivity and Direct Experimental Estimate of the Singlet/Triplet Energy Gap
The 2 references without a DOI — listed, not checked
no DOI — not checkedC8SC01165F-(cit2o)/*[position()=1]
no DOI — not checkedC8SC01165F-(cit18b)/*[position()=1]
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