536744-92-0Relevant articles and documents
Ruthenium-catalyzed alkyne-propargyl alcohol addition. An asymmetric total synthesis of (+)-alpha-kainic acid.
Trost, Barry M,Rudd, Michael T
, p. 1467 - 1470 (2003)
A novel route to the neuroexcitatory amino acid, kainic acid, is developed. The key concept derives from a ruthenium-catalyzed cycloisomerization of a tethered alkyne-propargyl alcohol to form a cyclic 2-vinyl-1-acyl compound. A single stereocenter introd
Ruthenium-catalyzed cycloisomerizations of diynols
Trost, Barry M.,Rudd, Michael T.
, p. 4763 - 4776 (2007/10/03)
A wide variety of diynols containing tertiary, secondary, and primary propargylic alcohols undergo a cycloisomerization reaction to form dienones and dienals in the presence of a catalytic amount of [CpRu(CH3CN) 3]PF6. The