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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

Indolence

Critical Quarterly, 2022
openaire   +1 more source

Research progress of indole compounds with potential antidiabetic activity

European Journal of Medicinal Chemistry, 2021
Yang Gao, He Bao, Hailong Zhang
exaly  

Indole alkaloids

1976
M. F. Grundon, J. E. Saxton
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Indolent lymphomas

Best Practice & Research Clinical Haematology, 2018
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Indoles

Chemistry of Heterocyclic Compounds, 1973
I. I. Grandberg, N. I. Bobrova
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Recent progress in biologically active indole hybrids: a mini review

Pharmacological Reports, 2022
Alaa M Hayallah   +2 more
exaly  

Indoles

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

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