1360649-35-9

Upstream product

• 1360649-09-7 2-(1-chloroprop-1-enyl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane 
• 61676-62-8 2-Isopropoxy-4,4,5,5-tetramethyl-1,3,2-dioxaborolane 
• 347389-75-7 4,4,5,5-tetramethyl-2-(prop-1-yn-1-yl)-1,3,2-dioxaborolane 

Relevant 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

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

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