Reference health
Conversion of Azides into Diazo Compounds in Water
63/63 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.
4 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 63 checked references that resolve
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Synthetic Applications of 1,3‐Dipolar Cycloaddition Chemistry Toward Heterocycles and Natural Products
resolves10.1002/anie.200904828
To Protonate or Alkylate? Stereoselective Brønsted Acid Catalysis of CC Bond Formation Using Diazoalkanes
resolves10.1016/S0040-4020(01)88298-3
Application of Intramolecular Carbenoid Reactions in Organic Synthesis
resolves10.1021/cr0200217
Catalytic Enantioselective C−H Activation by Means of Metal−Carbenoid-Induced C−H Insertion
resolves10.2174/157017906778699512
Rhodium(II)-Catalyzed Reaction of Diazocompounds in the Service of Organic Synthesis of Natural and Non-Natural Products
resolves10.1042/bj0680114
Studies on the amide and <i>C</i>-terminal residues in proteins. 3. The esterification of proteins
resolves10.1021/bi00880a023
Structural Studies of Ribonuclease. XVII. A Reactive Carboxyl Group in Ribonuclease<sup>*</sup>
resolves10.1021/ja047272c
Selective Tryptophan Modification with Rhodium Carbenoids in Aqueous Solution
resolves10.1021/ar300101k
Diazo Compounds and
<i>N</i>
-Tosylhydrazones: Novel Cross-Coupling Partners in Transition-Metal-Catalyzed Reactions
resolves10.1021/ja302284p
Catalytic Protein Modification with Dirhodium Metallopeptides: Specificity in Designed and Natural Systems
resolves10.1039/c2sc20806g
Diazo compounds as highly tunable reactants in 1,3-dipolar cycloaddition reactions with cycloalkynes
resolves10.1002/cber.188301602136
Ueber die Einwirkung von salpetriger Säure auf salzsauren Glycocolläther
resolves10.1080/00397918708063988
Diazotransfer Reactions with<i>p</i>-Acetamidobenzenesulfonyl Azide
resolves10.1021/jo00120a013
Advantageous Syntheses of Diazo Compounds by Oxidation of Hydrazones with Lead Tetraacetate in Basic Environments
resolves10.1021/ja0459779
A General Procedure for the Esterification of Carboxylic Acids with Diazoalkanes Generated in Situ by the Oxidation of <i>N</i>-<i>tert</i>-Butyldimethylsilylhydrazones with (Difluoroiodo)benzene
resolves10.1002/ejoc.200400700
The Use of Tosylhydrazone Salts as a Safe Alternative for Handling Diazo Compounds and Their Applications in Organic Synthesis
resolves10.1002/hlca.19190020164
Über neue organische Phosphorverbindungen III. Phosphinmethylenderivate und Phosphinimine
resolves10.1021/ol006739v
High-Yielding Staudinger Ligation of a Phosphinothioester and Azide To Form a Peptide
resolves10.1021/ja073204p
Water-Soluble Phosphinothiols for Traceless Staudinger Ligation and Integration with Expressed Protein Ligation
resolves10.1021/jo00094a044
Synthesis and Characterization of a Chiral Dendrimer Derived from Pentaerythritol
resolves10.1021/ja00169a036
Synthesis and reactions of phosphine-boranes. Synthesis of new bidentate ligands with homochiral phosphine centers via optically pure phosphine-boranes
resolves10.1016/j.tet.2009.05.063
Catalyst-free alcoholysis of phosphane-boranes: a smooth, cheap, and efficient deprotection procedure
resolves10.1039/tf9545000800
A spectrophotometric determination of the dissociation constants of p-nitrophenol and papaverine
resolves10.1055/s-2001-9697
Convenient Synthesis of a New Class of N<sub>2</sub>SO or N<sub>2</sub>S<sub>2</sub> Tetradentate Ligands Suitable for Nuclear Medicine Applications
resolves10.1021/ja808792x
A Single Antibody Catalyzes Multiple Chemical Transformations upon Replacement of the Functionalized Small Nonprotein Components
resolves10.1021/ic060236p
Scope and Limitations of the Base-Catalyzed Phospha-Peterson PC Bond-Forming Reaction
resolves10.1016/S0040-4039(03)00451-9
Efficient synthesis of functionalized 2,5-dihydro-1,2-oxaphospholes
resolves10.1016/j.bmc.2010.10.060
Design, synthesis and antimycobacterial activities of 1-methyl-2-alkenyl-4(1H)-quinolones
resolves10.1021/jo101864n
One-Pot Eschenmoser Episulfide Contractions in DMSO: Applications to the Synthesis of Fuligocandins A and B and a Number of Vinylogous Amides
resolves10.1016/0076-6879(77)47012-5
[10] Reductive cleavage of cystine disulfides with tributylphosphine
resolves10.1021/bi048329a
New Water-Soluble Phosphines as Reductants of Peptide and Protein Disulfide Bonds: Reactivity and Membrane Permeability
resolves10.1021/bm060192b
Fluorescent Labeling of RAFT-Generated Poly(<i>N</i>-isopropylacrylamide) via a Facile Maleimide−Thiol Coupling Reaction
resolves10.1039/B616298C
Mechanism of the sulfurisation of phosphines and phosphites using 3-amino-1,2,4-dithiazole-5-thione (xanthane hydride)
resolves10.1021/ja210335f
Polymeric Dibromomaleimides As Extremely Efficient Disulfide Bridging Bioconjugation and Pegylation Agents
resolves10.1016/j.tetlet.2003.08.068
CsOH-promoted epoxide ring-opening with phosphines: mild and efficient synthesis of monohydroxyphosphines
resolves10.1016/j.tetlet.2003.09.002
A novel procedure for conversion of epoxides to α-hydroxyphosphonates with a trialkylphosphite mediated by LiClO4
resolves10.1002/chem.200902915
Highly Modular POP Ligands for Asymmetric Hydrogenation: Synthesis, Catalytic Activity, and Mechanism
resolves10.1021/bi201075b
Bovine Pancreatic Ribonuclease: Fifty Years of the First Enzymatic Reaction Mechanism
The 4 references without a DOI — listed, not checked
no DOI — not checked1,3-Dipolar Cycloaddition Chemistry
no DOI — not checkedDiazo Compounds: Properties and Synthesis
no DOI — not checkedref3/cit3f
no DOI — not checkedref13/cit13
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