Results 21 to 30 of about 2,460 (195)

Catalyzed and uncatalyzed procedures for the syntheses of isomeric covalent multi-indolyl hetero non-metallides: an account

open access: yesBeilstein Journal of Organic Chemistry, 2021
Two or more indole molecules tailored to a single non-metal central atom, through any of their C2–7 positions are not only structurally engaging but also constitute a class of important pharmacophores.
Ranadeep Talukdar
doaj   +1 more source

Concise Syntheses of Marine (Bis)indole Alkaloids Meridianin C, D, F, and G and Scalaridine A via One-Pot Masuda Borylation-Suzuki Coupling Sequence

open access: yesMolecules, 2022
N-Protected 3-iodoindoles were reacted with (di)azine halides in a sequentially Pd-catalyzed one-pot fashion, i.e., by Masuda borylation–Suzuki coupling (MBSC) sequence.
Marco Kruppa   +2 more
doaj   +1 more source

Two new bisindole alkaloids from Tabernaemontana macrocarpa Jack [PDF]

open access: yesJournal of Natural Medicines, 2021
Two new bisindole alkaloids, bisnaecarpamines A (1) and B (2), possessing a vobasine-sarpagine type skeleton were isolated from the bark of Tabernaemontana macrocarpa Jack. Their structures were elucidated by extensive spectroscopic methods and chemical correlation.
Amelia, Puteri   +6 more
openaire   +2 more sources

CrERF5, an AP2/ERF Transcription Factor, Positively Regulates the Biosynthesis of Bisindole Alkaloids and Their Precursors in Catharanthus roseus

open access: yesFrontiers in Plant Science, 2019
Catharanthus roseus contains a variety of monoterpenoid indole alkaloids (MIAs), among which bisindole alkaloids vinblastine and vincristine are well-known to have antitumor effects and widely used in clinical treatment.
Qifang Pan   +9 more
doaj   +1 more source

Electrophilic carbonyl activation: competing condensative cyclizations of tryptamine derivatives [PDF]

open access: yes, 2014
A series of tryptamine derived bisindole substrates were subjected to electrophilic activation of the func-tional grouping at their [alpha]-nitrogen in the form of iminium ions to enable cyclization onto the sterically hindered indole substructure.
Liu, Fan, Movassaghi, Mohammad
core   +1 more source

Crystal structure of diethyl 3,3′-[(4-nitrophenyl)methylene]bis(1H-indole-2-carboxylate)

open access: yesActa Crystallographica Section E: Crystallographic Communications, 2017
In the title compound, C29H25N3O6, the mean planes of the two indole ring systems (r.m.s. deviations = 0.0115 and 0.0082 Å) are approximately perpendicular to one another, making a dihedral angle of 89.7 (5)°; the benzene ring is twisted with respect to ...
Hong-Shun Sun   +4 more
doaj   +1 more source

π-Conjugated Indole Dyads with Strong Blue Emission Made Possible by Stille Cross-Coupling and Double Fischer Indole Cyclisation [PDF]

open access: yes, 2017
Small fluorescent π-conjugated indolyl-based molecules 4–6, 23 are prepared through direct Fischer synthesis or/and Stille cross-coupling method in appreciable yields.
Garrote Cañas, A.M.   +2 more
core   +2 more sources

Diethyl 3,3′-[(4-fluorophenyl)methylidene]bis(1H-indole-2-carboxylate)

open access: yesIUCrData, 2019
In the title compound, C29H25FN2O4, the mean planes of the indole ring systems (r.m.s. deviations = 0.0107 and 0.0158 Å) are approximately perpendicular to each other, subtending a dihedral angle of 87.43 (16)°. The 4-fluorophenyl ring is twisted by 77.6 
Yu-Long Li   +6 more
doaj   +1 more source

Violacein: Properties and Production of a Versatile Bacterial Pigment [PDF]

open access: yes, 2015
Violacein-producing bacteria, with their striking purple hues, have undoubtedly piqued the curiosity of scientists since their first discovery. The bisindole violacein is formed by the condensation of two tryptophan molecules through the action of five ...
Choi. Seong Yeol   +3 more
core   +2 more sources

High-level production of violacein by the newly isolated Duganella violaceinigra str. NI28 and its impact on Staphylococcus aureus [PDF]

open access: yes, 2015
A violacein-producing bacterial strain was isolated and identified as a relative of Duganella violaceinigra YIM 31327 based upon phylogenetic analyses using the 16S rRNA, gyrB and vioA gene sequences and a fatty acid methyl ester (FAME) analysis.
AL Rodrigues   +37 more
core   +1 more source

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