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Volumn 20, Issue 20, 2014, Pages 6162-6170

Expanded-ring N-heterocyclic carbenes efficiently stabilize gold(I) cations, leading to high activity in π-acid-catalyzed cyclizations

(9) Morozov, Oleg S a Lunchev, Andrey V a Bush, Alexander A a Tukov, Aleksandr A a Asachenko, Andrey F a Khrustalev, Victor N b Zalesskiy, Sergey S c Ananikov, Valentine P c Nechaev, Mikhail S a,d

a TOPCHIEV INSTITUTE OF PETROCHEMICAL SYNTHESIS (Russian Federation)

b A N NESMEYANOV INSTITUTE OF ORGANOELEMENT COMPOUNDS (Russian Federation)

c N D ZELINSKY INSTITUTE OF ORGANIC CHEMISTRY (Russian Federation)

d MOSCOW STATE UNIVERSITY (Russian Federation)

Author keywords

alkynes; density functional theory; gold; hydroamination; N heterocyclic carbenes

Indexed keywords

CATALYSTS; CHLORINE COMPOUNDS; CYCLIZATION; DENSITY FUNCTIONAL THEORY; GOLD; GOLD COMPOUNDS; INORGANIC COMPOUNDS; NUCLEAR MAGNETIC RESONANCE SPECTROSCOPY; ORGANIC COMPOUNDS; PHOSPHORUS COMPOUNDS; POLYCYCLIC AROMATIC HYDROCARBONS; POSITIVE IONS; STABILIZATION; SYNTHESIS (CHEMICAL);

ALKYNES; CYCLIZATION REACTIONS; ELECTRON DONATING PROPERTIES; HYDROAMINATIONS; N-HETEROCYCLIC CARBENES; QUANTITATIVE YIELDS; SEVEN-MEMBERED RINGS; WEAKLY COORDINATING ANIONS;

CATALYST ACTIVITY;

EID: 84900020318 PISSN: 09476539 EISSN: 15213765 Source Type: Journal
DOI: 10.1002/chem.201303760 Document Type: Article

Times cited : (66)

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