125010-58-4Relevant articles and documents
Asymmetric Synthesis of Spiroketals with Aminothiourea Catalysts
Yoneda, Naoki,Fukata, Yukihiro,Asano, Keisuke,Matsubara, Seijiro
, p. 15497 - 15500 (2015)
Chiral spiroketal skeletons are found as core structures in a range of bioactive compounds. These natural compounds and their analogues have attracted much attention in the field of drug discovery. However, methods for their enantioselective construction are limited, and easily available optically active spiroketals are rare. We demonstrate a novel catalytic asymmetric synthesis of spiroketal compounds that proceeds through an intramolecular hemiacetalization/oxy-Michael addition cascade mediated by a bifunctional aminothiourea catalyst. This results in spiroketal structures through the relay formation of contiguous oxacycles, in which multipoint recognition by the catalyst through hydrogen bonding imparts high enantioselectivity. This method offers facile access to spiroketal frameworks bearing an alkyl group at the 2-position, which are prevalent in insect pheromones. Optically active (2S,5S)-chalcogran, a pheromone of the six-spined spruce bark beetle, and an azide derivative could be readily synthesized from the bicyclic reaction product. Around and around: A catalytic asymmetric synthesis of spiroketals through an intramolecular hemiacetalization/oxy-Michael addition cascade with a bifunctional aminothiourea catalyst was developed. This method offers facile access to spiroketal frameworks bearing an alkyl group at the 2-position. Optically active (2S,5S)-chalcogran, a pheromone from the six-spined spruce bark beetle, and a derivative were readily synthesized from the bicyclic reaction product.
Asymmetric transfer hydrogenation of quinolines using tethered Ru(II) catalysts
Parekh, Vimal,Ramsden, James A.,Wills, Martin
experimental part, p. 1549 - 1556 (2010/11/02)
The first report of an asymmetric transfer hydrogenation, in formic acid/triethylamine, of quinolines is described. Using a Ru(II) catalyst containing a 4-carbon tether, products of up to 73% ee were formed, whilst a Rh(III)-tethered catalyst gave products of up to 94% ee.
SYNTHESIS OF TWO INTERMEDIATE PHOSPHONIUM SALTS FOR 5,10 AND 15,20-DiHETES
Mosset, Paul,Gree, Rene,Falck, J. R.
, p. 645 - 658 (2007/10/02)
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