Results 281 to 290 of about 29,358 (323)
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Easy Access to 1-Amino and 1-Carbon Substituted Isoquinolines via Cobalt-Catalyzed CH/NO Bond Activation

, 2016
A green atom-economical method for the synthesis of highly functionalized 1-amino and 1-carbon substituted isoquinolines from the reaction of N′-hydroxybenzimidamides and aryl ketoximes, respectively, with alkynes via pentamethylcyclopentadienylcobalt ...
K. Muralirajan   +3 more
semanticscholar   +1 more source

Tandem Addition/Cyclization for Access to Isoquinolines and Isoquinolones via Catalytic Carbopalladation of Nitriles.

Organic Letters, 2017
The first example of the palladium-catalyzed sequential nucleophilic addition followed by an intramolecular cyclization of functionalized nitriles with arylboronic acids has been achieved, providing an efficient synthetic pathway to access structurally ...
Linjun Qi   +7 more
semanticscholar   +1 more source

Isoquinolines as receptors for resorcinol

Tetrahedron Letters, 1994
Abstract Multiple condensation reactions based on the Pictet-Gams isoquinoline synthesis lead to receptors for resorcinol. The host-guest interaction is confirmed by anisotropic highfield shifts and by NOE enhancement between aryl protons.
Gerald Dyker   +3 more
openaire   +2 more sources

Acid-Mediated Intermolecular [3 + 2] Cycloaddition toward Pyrrolo[2,1-a]isoquinolines: Total Synthesis of the Lamellarin Core and Lamellarin G Trimethyl Ether.

Organic Letters, 2017
A novel one-pot reaction has been developed for the efficient synthesis of pyrrolo[2,1-a]isoquinolines and 1-dearyllamellarin core from (E)-(2-nitrovinyl)benzenes and azomethine ylides generated in situ.
Kai-lu Zheng   +4 more
semanticscholar   +1 more source

Construction of Tropane Derivatives by the Organocatalytic Asymmetric Dearomatization of Isoquinolines.

Angewandte Chemie, 2016
A chiral-NHC-catalyzed highly diastereo- and enantioselective dearomatizing double Mannich reaction of isoquinolines was developed that provides a powerful and straightforward synthetic route toward substituted tropane derivatives with four contiguous ...
Jin-Hui Xu   +4 more
semanticscholar   +1 more source

Practical and Asymmetric Reductive Coupling of Isoquinolines Templated by Chiral Diborons.

Journal of the American Chemical Society, 2017
We herein describe a chiral diboron-templated highly diastereoselective and enantioselective reductive coupling of isoquinolines that provided expedited access to a series of chiral substituted bisisoquinolines in good yields and excellent ee's under ...
Dong-Li Chen   +4 more
semanticscholar   +1 more source

ChemInform Abstract: Synthesis of Benzimidazo(2,1‐a)isoquinolines and 5,6‐ Dihydrobenzimidazo(2,1‐a)isoquinolines.

ChemInform, 1996
AbstractChemInform is a weekly Abstracting Service, delivering concise information at a glance that was extracted from about 100 leading journals. To access a ChemInform Abstract of an article which was published elsewhere, please select a “Full Text” option. The original article is trackable via the “References” option.
Qun Sun, Edmond J. LaVoie
openaire   +3 more sources

Asymmetric Hydrogenation of Isoquinolines and Pyridines Using Hydrogen Halide Generated in Situ as Activator.

Organic Letters, 2017
By employing halogenide trichloroisocyanuric acid as a traceless activation reagent, a general iridium-catalyzed asymmetric hydrogenation of isoquinolines and pyridines is developed with up to 99% ee.
Mu-Wang Chen   +5 more
semanticscholar   +1 more source

Cobalt(III)-Catalyzed C-H/N-O Functionalizations: Isohypsic Access to Isoquinolines.

Chemistry, 2015
C-H/N-O functionalizations by cobalt(III) catalysis allowed the expedient synthesis of a broad range of isoquinolines. Thus, internal and challenging terminal alkynes proved to be viable substrates for an isohypsic annulation, which was shown to proceed ...
Hui Wang   +3 more
semanticscholar   +1 more source

Cyanochlorination and cyanation of isoquinolines

Journal of the Chemical Society, Perkin Transactions 1, 1979
Treatment of isoquinoline with sulphuryl chloride and potassium cyanide gave, in one preparative step, 4-chloro-1-cyanoisoquinoline and 1-carbamoyl-3-cyanoisoquinoline in yields dependent upon the proportions of reagents. 4-Chloroisoquinoline, 1,3-dicyanoisoquinoline, 3-cyanoisoquinoline, and 1-cyanoisoquinoline were also produced under different ...
Seng Leong Tan   +2 more
openaire   +2 more sources

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