We report a BF3-mediated novel dehydrative cycloaddition reaction of benzoquinones with stilbene oxides to afford 2,3-diaryl-5-hydroxybenzofurans and 2,3-diaryl-5-hydroxydihydrobenzofurans in good combined yields. No change in the products or the yield is observed when using diphenylacetaldehyde and cis-stilbene oxide instead of trans-stilbene oxides. When stilbene oxide is reacted with hydroquinone
APPARATUS AND METHOD FOR CARRYING OUT MULTIPLE REACTIONS
申请人:Bowden Ned
公开号:US20090299102A1
公开(公告)日:2009-12-03
The invention provides methods and an apparatus useful for site-isolating reagents or catalysts during chemical reactions. The methods and apparatus are useful for carrying out cascade or domino reactions.
The indiumâbipyridine-catalyzed, enantioselective ring-opening of meso-epoxides with aliphatic and aromatic thiols furnished 1,2-mercapto alcohols in good yields and excellent enantioselectivities; the crystal structure of the chiral catalyst reveals a pentagonal-bipyramidal coordination geometry around the indium center.
Copper-catalyzed aerobic oxidative cleavage of C–C bonds in epoxides leading to aryl nitriles and aryl aldehydes
作者:Lijun Gu、Cheng Jin
DOI:10.1039/c5cc00360a
日期:——
Novel copper-catalyzedaerobic synthesis of aryl nitriles and aldehydes from epoxides via C-C single bond cleavage has been discovered. This reaction provides a practical method toward the synthesis of aryl nitriles and aldehydes, which are versatile intermediates and building blocks in organic synthesis.