Javascript must be enabled to continue!
Indazole
View through CrossRef
Abstract
Indazole
intermediate: 2‐hydroxymethylenecyclohexanone
solvent: 100 ml. of hot petroleum ether
intermediate: 4,5,6,7‐tetrahydroindazole
product: indazole
Title: Indazole
Description:
Abstract
Indazole
intermediate: 2‐hydroxymethylenecyclohexanone
solvent: 100 ml.
of hot petroleum ether
intermediate: 4,5,6,7‐tetrahydroindazole
product: indazole.
Related Results
[3+2] Cycloaddition of 3‐Diazooxindole with Arynes for the Synthesis of Spiro[indazole‐3,3′‐indolin]‐2′‐ones
[3+2] Cycloaddition of 3‐Diazooxindole with Arynes for the Synthesis of Spiro[indazole‐3,3′‐indolin]‐2′‐ones
AbstractAn intermolecular cycloaddition between 3‐diazooxindoles and arynes generated in situ from 2‐(trimethylsilyl)phenyltrifluoromethanesulfonate in the presence of 2.5 mol% ces...
Dispersed Fluorescence Spectra of 1H- and 1D-Indazole
Dispersed Fluorescence Spectra of 1H- and 1D-Indazole
Abstract
Dispersed fluorescence (DF) spectra of jet-cooled indazole (Ia-h) and its singly-deuterated isotopologue (Ia-d) were recorded following excitation of the or...
Anticancer Ruthenium(III) Complex KP1019 Interferes with ATP‐Dependent Ca2+ Translocation by Sarco‐Endoplasmic Reticulum Ca2+‐ATPase (SERCA)
Anticancer Ruthenium(III) Complex KP1019 Interferes with ATP‐Dependent Ca2+ Translocation by Sarco‐Endoplasmic Reticulum Ca2+‐ATPase (SERCA)
AbstractSarco‐endoplasmic reticulum Ca2+‐ATPase (SERCA), a P‐type ATPase that sustains Ca2+ transport and plays a major role in intracellular Ca2+ homeostasis, represents a therape...
Synthesis, Bioactivity Evaluation, and Molecular Docking Study of Novel 1-(5-methoxy-2,2-dimethyl-2H-chromen-6-yl) urea derivatives as Anticancer Agents
Synthesis, Bioactivity Evaluation, and Molecular Docking Study of Novel 1-(5-methoxy-2,2-dimethyl-2H-chromen-6-yl) urea derivatives as Anticancer Agents
This study aims to design, synthesize, and evaluate novel 1-(5-methoxy-2,2-dimethyl-2H-chromen-6-yl) urea derivatives based on a deguelin-truncated carboxamide scaffold as anticanc...
Eschenmoser Coupling Reaction and Reactivity of Hydrazinecarbothioamides in the Synthesis of Benzindazole and Naphthothiazole Derivatives
Eschenmoser Coupling Reaction and Reactivity of Hydrazinecarbothioamides in the Synthesis of Benzindazole and Naphthothiazole Derivatives
N-Unsubstituted and N-substituted 2-phenylhydrazinecarbothioamides react with 2,3-dichloro-1,4-naphthoquinone to give a series of unprecedented 3-amino- and 3-(alkylamino)-1-phenyl...

