Results 281 to 290 of about 29,358 (323)
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, 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
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
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
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, 1994Abstract 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
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
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
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
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, 2017We 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, 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
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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
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
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, 2015C-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, 1979Treatment 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