Results 1 to 10 of about 17,074 (296)
Highly Enantioselective Partial Hydrogenation of Simple Pyrroles: A Facile Access to Chiral 1-PyrrolinesA highly enantioselective Pd-catalyzed partial hydrogenation of simple 2,5-disubstituted pyrroles with a Bronsted acid as an activator has been ...
Duo-Sheng Wang +2 more
exaly +2 more sources
B(C6F5)3-Catalyzed Dehydrogenation of Pyrrolidines to Form Pyrroles
Pyrroles are important N-heterocycles found in medicines and materials. The formation of pyrroles from widely accessible pyrrolidines is a potentially attractive strategy but is an underdeveloped approach due to the sensitivity of pyrroles to the ...
Rebecca R Hawker +2 more
exaly +2 more sources
Some of the next articles are maybe not open access.
β-Selective C–H Arylation of Pyrroles Leading to Concise Syntheses of Lamellarins C and I
Journal of the American Chemical Society, 2014Kirika Ueda +2 more
exaly
General and Regioselective Synthesis of Pyrroles via Ruthenium-Catalyzed Multicomponent Reactions
Journal of the American Chemical Society, 2013Xianjie Fang +2 more
exaly
Synthesis of novel pyrroles and fused pyrroles as antifungal and antibacterial agents [PDF]
Pyrroles and its fused forms possess antimicrobial activities, they can easily interact with biomolecules of living systems. A series of substituted pyrroles, and its fused pyrimidines and triazines forms have been synthesised, all newly synthesised ...
Zainab M Khoder
exaly +4 more sources
Environmentally Friendly Synthesis of Polysubstituted Pyrroles in Ionic Liquid via Gold-Catalyzed Propargylic Substitution/Hydration/Amination/Cycloisomerization Sequence [PDF]
An environmentally friendly synthesis of polysubstituted pyrroles in ionic liquid was achieved via a gold-catalyzed propargylic substitution/hydration/amination/cycloisomerization sequence. Treatment of propargylic alcohols, 1,3-dicarbonyl compounds, and
Hitomi Chiaki +3 more
doaj +2 more sources
A stepwise synthesis of a-unsubstituted pyrroles with desired substituents in the b-positions of the ring has been devised.
O. A. Golubchicov +2 more
doaj +2 more sources

