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Nickel/Photoredox-Catalyzed Asymmetric Reductive Cross-Coupling of Racemic a-Chloro Esters with Aryl Iodides.

Angewandte Chemie, 2020
A unique nickel/organic photoredox co-catalyzed asymmetric reductive cross-coupling between a-chloro esters and aryl iodides is advanced.  This cross-electrophile coupling reaction employs an organic reductant (Hantzsch ester), whereas most reductive ...
Haixing Guan   +3 more
semanticscholar   +1 more source

Bufotenine esters

Journal of Medicinal Chemistry, 1979
Bufotenine (5-hydroxy-N,N-dimethyltryptamine) has been reported to be behaviorally inactive or only very weakly active in man and animals; this may be a consequence of its low partition coefficient and resultant inability to penetrate the blood--brain barrier.
R A, Glennon   +3 more
openaire   +2 more sources

Iodomethaneboronic esters and aminomethaneboronic esters

Journal of Organometallic Chemistry, 1979
Abstract An efficient preparation of pinacol iodomethaneboronate and dibutyl iodomethaneboronate from the respective (phenylthio)methaneboronic esters has been devised, using the reaction with methyl iodide. Pinacol iodomethaneboronate reacts efficiently wit tertiary amines to form the crystalline quaternary ammonium salts.
Donald S. Matteson, Debesh Majumdar
openaire   +1 more source

Copper-Catalyzed Radical Cross-Coupling of Redox-Active Oxime Esters, Styrenes, and Boronic Acids.

Angewandte Chemie, 2018
A visible-light-driven, copper-catalyzed three-component radical cross-coupling of oxime esters, styrenes, and boronic acids has been developed. Key steps of this protocol involve catalytic generation of an iminyl radical from a redox-active oxime ester ...
Xiao‐Ye Yu   +4 more
semanticscholar   +1 more source

Esters

ChemInform, 1990
AbstractFor Abstract see ChemInform Abstract in Full Text.
openaire   +1 more source

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