Results 11 to 20 of about 41,236 (276)

Indoles [PDF]

open access: yes, 2018
Embedded medium-sized carbacycles and cyclohepta [b] indoles occur frequently as scaffold elements in natural products and bioactive compounds. Described herein is a conceptionally novel photochemically triggered cascade process to these scaffolds.
Navriti Chadha, Om Silakari
openaire   +2 more sources

Efficient copper-catalyzed synthesis of C3-alkylated indoles from indoles and alcohols [PDF]

open access: yes, 2021
A highly efficient copper(II) catalyst system for alkylation of indoles with alcohols via hydrogen borrowing method has been developed to afford C3-alkylated indoles in good to excellent yields. Cu(OAc)2 in the combination with dppm ligand has been found
Van Phuc, Ban   +6 more
core   +1 more source

When Is an Indole Not an Indole? [PDF]

open access: yesClinical Chemistry, 1998
An indole is not an indole when it is a naphthalene derivative! We routinely measure 5-hydroxyindoleacetic acid (5HIAA) by a long-established method using nitrosonaphthol, as first described by Udenfriend in 1955 (1), but with various modifications to improve specificity (2).
Kathryn Brownbill, John A Martin
openaire   +1 more source

Diastereoselective Access to Triazolo[1,2‑a]indolines via a Bio-Inspired Oxidative Cyclization of NH-Indoles [PDF]

open access: yes, 2022
Establishing three-dimensional chemicals by using the C2–C3 π bond of indoles has always been a research hotspot in organic synthesis; however, employing the oxidative C2–C3 π bond of indoles to generate imine which would lead to the N1–C2 π bond ...
Kui Du (3488084)   +6 more
core   +1 more source

Programmable Deuteration of Indoles via Reverse Deuterium Exchange [PDF]

open access: yes, 2023
Methods for selective deuterium incorporation into drug-like molecules have become extremely valuable due to the commercial, mechanistic, and biological importance of deuterated compounds.
Greener, Andrew   +3 more
core   +2 more sources

Undirected, Pd-catalysed deuteration of indoles with programmable regioselectivity [PDF]

open access: yes, 2022
Methods for selective deuterium-incorporation into drug-like molecules have become extremely valuable due to the commercial and biological importance of deuterated compounds.
Rachael, McNulty   +3 more
core   +1 more source

Umpolung of Indoles: Triflic Acid-Mediated C3-Regioselective Hydroarylation of N-H Indoles [PDF]

open access: yes, 2022
The direct dearomative addition of arenes to the C3-position of unprotected indoles is reported under operationally simple condi-tions, using triflic acid at room temperature.
Vincent, Gandon   +4 more
core   +1 more source

Identification of novel flavin-dependent monooxygenase from Strobilanthes Cusia reveals molecular basis of indoles’ biosynthetic logic

open access: yesBMC Plant Biology, 2023
Background Strobilanthes cusia (Nees) Kuntze is a traditional medical plant distributed widely in south China. The indole compounds that originated from the plant are responsible for its pharmacological activities.
Chang Liu   +4 more
doaj   +1 more source

Natural Indole Alkaloids from Marine Fungi: Chemical Diversity and Biological Activities

open access: yesPharmaceutical Fronts, 2021
The indole scaffold is one of the most important heterocyclic ring systems for pharmaceutical development, and serves as an active moiety in several clinical drugs.
Jiao Li, Chun-Lin Zhuang
doaj   +1 more source

Oxidative Dearomative Cross-Dehydrogenative Coupling of Indoles with Diverse C-H Nucleophiles: Efficient Approach to 2,2-Disubstituted Indolin-3-ones

open access: yesMolecules, 2020
The oxidative, dearomative cross-dehydrogenative coupling of indoles with various C-H nucleophiles is developed. This process features a broad substrate scope with respect to both indoles and nucleophiles, affording structurally diverse 2,2-disubstituted
Xue Yan   +4 more
doaj   +1 more source

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