914480-70-9Relevant academic research and scientific papers
Ring-closing metathesis as a tool for the efficient preparation of chiral spirocyclic ethers from homoallylic alcohols
Rosenberg, Sara,Leino, Reko
experimental part, p. 5305 - 5307 (2009/12/06)
The preparation of chiral spirocyclic ethers via allylic etherification/olefin metathesis of homoallylic alcohols is investigated. This reaction sequence transforms the enantiopure substrate alcohols, synthesized by a one-pot asymmetric rhodium-catalyzed
Highly enantio- and diastereoselective one-pot reactions in aqueous media: Combined asymmetric Rh-catalyzed conjugate addition/metal-mediated allylation
Kaellstroem, Sara,Jagt, Richard B. C.,Sillanpaeae, Reijo,Feringa, Ben L.,Minnaard, Adriaan J.,Leino, Reko
, p. 3826 - 3833 (2007/10/03)
1,3-Disubstituted, enantiopure cyclohexanols have been prepared in very high diastereoselectivities and good yields by a concise one-pot method combining the enantioselective rhodium-catalyzed conjugate addition of arylboronic acids with indium-mediated a
