1259299-94-9Relevant academic research and scientific papers
A practical synthetic approach to chiral (α-chloroalkyl)boronic esters via iridium-catalyzed chemoselective hydrogenation of chloro-substituted alkenyl boronates
Roseblade, Stephenj.,Casas-Arce, Eva,Nettekoven, Ulrike,Gazic Smilovic, Ivana,Zanotti-Gerosa, Antonio,Casar, Zdenko
, p. 2824 - 2831 (2013/10/22)
Chiral (α-chloroalkyl)boronic esters are obtained by homogeneous asymmetric iridium-catalyzed chemoselective hydrogenation of (1-chloro-1-alkenyl)boronic esters. P,N-Iridium catalysis provides low level of dehalogenation during the hydrogenation, while th
Iridium-catalyzed chemoselective and enantioselective hydrogenation of (1-Chloro-1-Alkenyl) boronic esters
Gazi?smilovi?, Ivana,Casas-Arcé, Eva,Roseblade, Stephen J.,Nettekoven, Ulrike,Zanotti-Gerosa, Antonio,Kova?evi?, Miroslav,?asar, Zdenko
, p. 1014 - 1018 (2012/03/27)
Persistent chlorine: Hydrogenation of borolane-substituted vinylic chlorides catalyzed by Ir-P N complexes greatly preserved the chlorine substituent on the hydrogenated product, with only 3-19 % of dechlorinated byproducts present after hydrogenation. Th
NEW SYNTHETIC ROUTE FOR THE PREPARATION OF α-AMINO BORONIC ACID DERIVATIVES VIA SUBSTITUTED ALK-1-YNES
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Page/Page column 46, (2010/12/31)
The present invention relates in general to the field of organic chemistry and in particular to the preparation of α-amino boronic acid derivatives.
