Results 301 to 310 of about 172,313 (331)
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Ruthenium(II)-Catalyzed C-H Activation of Imidamides and Divergent Couplings with Diazo Compounds: Substrate-Controlled Synthesis of Indoles and 3H-Indoles.

Angewandte Chemie, 2016
Indoles are an important structural motif that is commonly found in biologically active molecules. In this work, conditions for divergent couplings between imidamides and acceptor-acceptor diazo compounds were developed that afforded NH indoles and 3H ...
Yunyun Li   +4 more
semanticscholar   +1 more source

Thiocyanation of indoles

Journal of Heterocyclic Chemistry, 1978
AbstractTreatment of indole, 2‐phenylindole, 2‐methylindole, and ethyl indole‐2‐carboxylate with thiocyanogen in acetic acid at 0° afforded the corresponding 3‐thiocyanatoindoles in quantitative yields, whereas similar treatment of 3‐methyl‐2‐phenylindoles and 2,3‐diphenylindoles gave the corresponding 6‐thiocyanatoindoles in high yields.
Sundo Kwon   +3 more
openaire   +2 more sources

Silver-Mediated Intermolecular 1,2-Alkylarylation of Styrenes with α-Carbonyl Alkyl Bromides and Indoles.

Angewandte Chemie, 2016
A new iron-facilitated silver-mediated radical 1,2-alkylarylation of styrenes with α-carbonyl alkyl bromides and indoles is described, and two new C-C bonds were generated in a single step through a sequence of intermolecular C(sp(3)-Br functionalization
Xuan-Hui Ouyang   +4 more
semanticscholar   +1 more source

Copper-Catalyzed Three-Component Reaction for Regioselective Aryl- and Heteroarylselenation of Indoles using Selenium Powder.

Journal of Organic Chemistry, 2016
A new and efficient copper-catalyzed C3 aryl- and heteroarylselenation of indoles employing selenium powder has been developed. The advantages of this chemistry involve the use of cheap selenating reagents, tolerance of a variety of functional groups ...
Dong‐Fen Luo   +7 more
semanticscholar   +1 more source

Ruthenium-Catalyzed, Site-Selective C-H Allylation of Indoles with Allyl Alcohols as Coupling Partners.

Organic Letters, 2016
A new ruthenium-catalyzed, heteroatom-directed strategy for C-H allylation of indoles is described. The use of allyl alcohols as coupling partners as well as pyridine as the removable directing group is highlighted. This methodology provides access to C2-
G. S. Kumar, M. Kapur
semanticscholar   +1 more source

Untersuchungen zur Indol-3-essigsäure-Bildung aus Indol,Indol-3-glycerin und Indol-3-glycerinphosphat

Flora oder Allgemeine botanische Zeitung. Abt. A, Physiologie und Biochemie, 1969
Summary Indole or indoleglycerol phosphate were incubated with crude or dialyzed enzyme extracts (pH 5.4-8.0) of pea seedlings. Neither with nor without addition of serine-like cosubstrates, any formation of auxin or an auxin precursor could be detected by means of the Avena curvature test or thin-layer chromatography.
N. Von Erdmann   +2 more
openaire   +2 more sources

Enantioselective Arylative Dearomatization of Indoles via Pd-Catalyzed Intramolecular Reductive Heck Reactions.

Journal of the American Chemical Society, 2015
A highly enantioselective intramolecular arylative dearomatization of indoles via palladium-catalyzed reductive Heck reactions was developed. The new strategy led to a series of optically active indolines bearing C2-quaternary stereocenters in modest to ...
Chong Shen   +6 more
semanticscholar   +1 more source

The tritylation of indole

Chemistry of Heterocyclic Compounds, 1970
Contrary to information in the literature, the reaction of indole with chlorotriphenylmethane forms not N-tritylindole but β-tritylindole.
P. F. Butskus, N. V. Raguotene
openaire   +2 more sources

Hegedus indole synthesis

2002
Stoichiometric Pd(II)-mediated oxidative cyclization of alkenyl anilines to indoles. Cf. Wacker oxidation.
openaire   +2 more sources

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