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Indoles

1992
This chapter focuses on indoles. Fusion of a benzene ring onto the C2/C3 positions of pyrrole formally produces the corresponding benzopyrrole known as indole. Indole is a ten π-electron aromatic system. As with pyrrole, delocalization of the lone pair of electrons from the nitrogen atom is necessary for aromaticity.
openaire   +1 more source

Indoles

Chemistry of Heterocyclic Compounds, 1978
N. M. Przheval'skii   +3 more
openaire   +1 more source

Indolent lymphomas

Best Practice & Research Clinical Haematology, 2018
openaire   +2 more sources

Practical Methodologies for the Synthesis of Indoles

Chemical Reviews, 2006
Guy R Humphrey
exaly  

Indoles

Chemistry of Heterocyclic Compounds, 1973
I. I. Grandberg, N. I. Bobrova
openaire   +2 more sources

Synthesis of Indoles through Domino Reactions of 2‐Fluorotoluenes and Nitriles

Angewandte Chemie - International Edition, 2019
Jianyou Mao   +2 more
exaly  

The Copper-Catalyzed N-Arylation of Indoles

Journal of the American Chemical Society, 2002
Jon C Antilla   +2 more
exaly  

Palladium-Catalyzed C3-Benzylation of Indoles

Journal of the American Chemical Society, 2012
Ye Zhu, Viresh H Rawal
exaly  

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