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Oxindole (2-indolone) is an
aromatic heterocyclic organic compound with the
formula C6H4CHC(O)NH. It has a
bicyclic structure,
consisting of a six-membered...
- The
Hinsberg oxindole synthesis is a
method of
preparing oxindoles from the
bisulfite additions of glyoxal. It is
named after its
inventor Oscar Hinsberg...
- Mitraphylline, an
oxindole derivative, is an
active alkaloid in the
leaves of the tree
Mitragyna speciosa,
commonly known as kratom. As a non-narcotic...
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Indigo can be
converted to
isatin and then to
oxindole. Then, in 1866,
Adolf von
Baeyer reduced oxindole to
indole using zinc dust. In 1869, he proposed...
-
Receptor Function:
Pharmacological Characterization of
Minor Indole and
Oxindole Alkaloids from Kratom". ACS
Chemical Neuroscience. 12 (14): 2661–2678....
- PDP (9-(6-phenyl-2-oxohex-3-yl)-2-(3,4-dimethoxybenzyl)-purin-6-one) and
oxindole. The
table above shows the
potency of PDE2
inhibitors including EHNA. There...
- Javier; Kiser, E. Jason; Shine,
Russell J.; Chen,
Michael H. (2013). "
Oxindole Synthesis via Palladium-catalyzed C-H Functionalization".
Organic Syntheses...
- 2-Chlorostyrene 2039-87-4 C8H7N
indole 120-72-9 C8H7NO indol-4-ol 2380-94-1
oxindole 59-48-3 5-hydroxyindole 1953-54-4 C8H8
cubane 277-10-1 C8H8N2OS...
-
works Julian synthesized the ring of
physostigmine from 1-methyl-3-formyl-
oxindole as
starting material,
which was
discovered by Paul Friedländer. However...
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family Rubiaceae.
Phytochemicals in
Uncaria tomentosa root bark
include oxindole and
indole alkaloids, glycosides,
organic acids, proanthocyanidins, sterols...