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Diazo compounds

Known as: diazo compound 
 
National Institutes of Health

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Related topics

3 relations

Broader (2)

Azo CompoundsDyes

Narrower (1)

Trypan Blue

Papers overview

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2017
2017
Rapid Asymmetric Synthesis of Disubstituted Allenes by Coupling of Flow‐Generated Diazo Compounds and Propargylated Amines
We report herein the asymmetric coupling of flow-generated unstabilized diazo compounds and propargylated amine derivatives… Expand
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2017
2017
Highly para-Selective C-H Alkylation of Benzene Derivatives with 2,2,2-Trifluoroethyl α-Aryl-α-Diazoesters.
Compared to the most popular directing-group-assisted strategy, the "undirected" strategy for C-H bond functionalization… Expand
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2016
2016
Ruthenium(II)-Catalyzed C-H Activation of Imidamides and Divergent Couplings with Diazo Compounds: Substrate-Controlled Synthesis of Indoles and 3H-Indoles.
Indoles are an important structural motif that is commonly found in biologically active molecules. In this work, conditions for… Expand
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2015
2015
Gold(I)-catalyzed diazo cross-coupling: a selective and ligand-controlled denitrogenation/cyclization cascade.
An unprecedented gold-catalyzed ligand-controlled cross-coupling of diazo compounds by sequential selective denitrogenation and… Expand
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2014
2014
Organocatalytic one-pot synthesis of highly substituted pyridazines from Morita-Baylis-Hillman carbonates and diazo compounds.
A biologically inspired organocatalytic one-pot synthesis of highly functionalized pyridazines, which are ubiquitous structural… Expand
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2014
2014
Potassium N-Iodo p-Toluenesulfonamide (TsNIK, Iodamine-T): A New Reagent for the Oxidation of Hydrazones to Diazo Compounds
A new reagent for the oxidation of hydrazones to diazo compounds is described. N-Iodo p-toluenesulfonamide (TsNIK, iodamine-T… Expand
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2013
2013
C-(α-d-Glucopyranosyl)-phenyldiazomethanes-irreversible inhibitors of α-glucosidase.
Several C-(α-d-glucopyranosyl)-phenyldiazomethanes, with different substituent groups at the para-position of the phenyl ring… Expand
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2013
2013
Catalytic asymmetric homologation of α-ketoesters with α-diazoesters: synthesis of succinate derivatives with chiral quaternary centers.
The one-carbon homologation of carbonyl compounds using diazo compounds is a frequently encountered synthetic objective. Several… Expand
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2011
2011
Çeşitli Karbonilli Diazo Bileşikleriyle, Bis-karbonilli Doymamış Bileşiklerin Sentezi
 
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1993
1993
Delay-time stable chemically amplified deep-UV resist
This paper describes a newly developed acetal-based positive tone deep UV photoresist called DX 46. The material consists of a 4… Expand
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