Premium
Homoleptic Lanthanide Amides as Homogeneous Catalysts for Alkyne Hydroamination and the Tishchenko Reaction
Author(s) -
Bürgstein Markus R.,
Berberich Helga,
Roesky Peter W.
Publication year - 2001
Publication title -
chemistry – a european journal
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.687
H-Index - 242
eISSN - 1521-3765
pISSN - 0947-6539
DOI - 10.1002/1521-3765(20010716)7:14<3078::aid-chem3078>3.0.co;2-e
Subject(s) - hydroamination , homoleptic , chemistry , lanthanide , catalysis , substrate (aquarium) , metallocene , combinatorial chemistry , organic chemistry , metal , polymerization , ion , oceanography , geology , polymer
The homoleptic bis(trimethylsilyl)amides of Group 3 metals and lanthanides of the general type [Ln{N(SiMe 3 ) 2 } 3 ] ( 1 ) (Ln=Y, lanthanide) represent a new class of Tishchenko precatalysts and, to a limited extent, precatalysts for the hydroamination/cyclization of aminoalkynes. It is shown that 1 is the most active catalyst for the Tishchenko reaction. This contribution presents investigations on the scope of the reaction, substrate selectivity, lanthanide‐ion size‐effect, and kinetic/mechanistic aspects of the Tishchenko reaction catalyzed by 1 . The turnover frequency is increased by the use of large‐center metals and electron‐withdrawing substrates. The reaction rate is second order with respect to the substrate. While donor atoms, such as nitrogen, oxygen, or sulfur, on the substrate decrease the turnover frequency, 1 shows a tolerance for a large number of functional groups. For the hydroamination/cyclization of aminoalkynes, 1 is less active than the well‐known metallocene catalysts. On the other hand, 1 is much more readily accessible (one‐step synthesis or commercially available), than the metallocenes and might therefore be an attractive alternative catalyst.