Results 31 to 40 of about 13,653 (252)

Tricyclic Imidazolidin-4-ones by Witkop Oxidation of Tetrahydro-β-carbolines

open access: yes, 2020
1-Substituted and 1,1-disubstituted tetrahydro-β-carbolines undergo sodium periodate oxidative ring expansion in the presence of formaldehyde and other aldehydes to form 5,6-dihydro-7H-1,4-methano­benzo­[e]­[1,4]­diazonine-2,7­(3H)-diones in 30–81% yield.
Douglas E. Stack (2429443)   +6 more
core   +2 more sources

Bioactivity of selected materials for coffee substitute. [PDF]

open access: yesPLoS ONE, 2018
Epidemiological studies have suggested that coffee consumption is negatively correlated with the incidence of Parkinson's disease. Coffee contains relatively high levels of β-carbolines, which have been ascribed neuroactive effects in humans however the ...
Renata Zawirska-Wojtasiak   +4 more
doaj   +1 more source

2-(2,5-Dimethoxyphenyl)pyrrole-3-carbonitrile

open access: yesMolbank, 2023
The Cadogan reaction of 2-aryl-3-nitropyridines leads to δ-carbolines. The title compound is a side product in this reaction, generated via a ring opening of a nitrene and cyclization. A crystal structure analysis gives an enormous unit cell.
Yannic Grimm   +2 more
doaj   +1 more source

β-Carboline (norharman) [PDF]

open access: yesActa Crystallographica Section C Crystal Structure Communications, 2011
The structure of β-carboline, also called norharman (systematic name: 9H-pyrido[3,4-b]indole), C(11)H(8)N(2), has been determined at 110 K. Norharman is prevalent in the environment and the human body and is of wide biological interest. The structure exhibits intermolecular N-H···N hydrogen bonding, which results in a one-dimensional herringbone motif.
Robert J, Thatcher   +1 more
openaire   +2 more sources

Enantioconvergent iso-Pictet-Spengler Reactions: Organocatalytic Synthesis of Chiral Tetrahydro-γ-carbolines

open access: yes, 2023
Enantioconvergent iso-Pictet-Spengler reactions of chiral racemic ß-formyl esters and a ß-keto ester are reported, providing complex tetrahydro-γ-carbolines containing two contiguous stereocenters.
Jeffrey S. Johnson (1312380)   +5 more
core   +1 more source

Expanding the scope of the Bohlmann-Rahtz reaction: new routes to 3-nitropyridines, ?-carbolines, and ß-carbolines

open access: yes, 2022
Chapter One opens with an overview of the role of pyridines in the pharmaceutical industry. This is followed by an in-depth survey of literature methods that have been reported for pyridine synthesis, including the Bohlmann-Rahtz reaction.
Tyler Nichols (4466107)
core   +1 more source

Mild and efficient ammonium chloride catalyzed Greener synthesis of tetrahydro-β-carboline

open access: yesCurrent Research in Green and Sustainable Chemistry, 2022
This protocol involves the NH4Cl catalyzed Pictet−Spengler reactions of tryptamine and arylaldehydes in anhydrous MeOH solvent to gives corresponding tetrahydro-β-carbolines (THβC) with 90% yield. This methodology offers mild, efficient and green reagent
Milind V. Gaikwad   +2 more
doaj   +1 more source

The Simultaneous Formation of Acrylamide, β-carbolines, and Advanced Glycation End Products in a Chemical Model System: Effect of Multiple Precursor Amino Acids

open access: yesFrontiers in Nutrition, 2022
This study investigated the effect of multiple precursor amino acids on the simultaneous formation of acrylamide, β-carbolines (i. e., harmane and norharmane), and advanced glycation end products (AGEs) [i.e., Nε-(carboxymethyl)lysine and Nε ...
Cuyu Chen   +8 more
doaj   +1 more source

Reactions of carboline [PDF]

open access: yesJournal of Spectroscopy, 1997
The reactions of carboline under various oxidative conditions are reported. The soft aerobic radiolysis, hydroxylation and rearrangement transformations are studied using isotopic labelling and GC–MS techniques.
Christophe Dardonville   +3 more
openaire   +1 more source

Electrochemical Oxidative Rearrangement of Tetrahydro-β-carbolines in Zero-gap Flow Cell [PDF]

open access: yes, 2022
Oxidative rearrangement of tetrahydro-β-carbolines (THβCs) is one of the most widely used reactions for the synthesis of biologically active spirooxindoles (natural products and drug molecules).
Yiting, Zheng   +8 more
core   +1 more source

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