Big Chemical Encyclopedia

Chemical substances, components, reactions, process design ...

Articles Figures Tables About
0 | 1 | 2 | 3 | 4 | 5 | 6 | 7 | 8 | 9 | a | b | c | d | e | f | g | h | i | j | k | l | m | n | o | p | q | r | s | t | u | v | w | x | y | z

   |<      <<      >>     > |    


Transfer functions of the motions of the secondary mirror M2 due to wind load on OWL

Transfer functions of TMD s stroke

Transfer functions ofdisplacement and acceleration at roof of the experimental building near the first and second modal frequencies with and without MTMD

Transfer Hopper to Blender Bucket

Transfer hydrogenation for a diltiazem intermediate

Transfer hydrogenation mediated by Rh complexes

Transfer hydrogenation of -keto-a-methylamino acid esters.

Transfer hydrogenation of 2 substituted quinolines to tetrahydroquinolines.

Transfer hydrogenation of 2-alkyl-l,3-diketones.

Transfer hydrogenation of 2-methyl-2,4-diaryl-2,3-dihydrobenzodiazepines.

Transfer hydrogenation of 2-substituted quinolines

Transfer hydrogenation of 4-acetylbenzophenone in the presence of catalysts P-3 and P-4. The product distribution after 1 h is reported .

Transfer hydrogenation of a imino esters having an alkynyl

Transfer hydrogenation of a mixture of seven different ketones . The conversion percent shows the product distribution after 20 min of reaction time. The numbers in parentheses correspond to the ratio of percentage conversion in the presence of P-3 to P-4.

Transfer hydrogenation of a-imino esters

Transfer hydrogenation of acetophenone in Galden D-100.

Transfer hydrogenation of acetophenone mediated by NHCP ruthenium complexes.

Transfer hydrogenation of acetophenone.

Transfer hydrogenation of acyclic ketimines using Hantzsch ester

Transfer hydrogenation of aldehydes using 2 TPPTS at 80 C using i-PrOH as hydrogen donor. Values shown are yields .

Transfer hydrogenation of aldehydes with catalyst 13 in water.

Transfer hydrogenation of aldehydes with Ir-PTsEN catalyst in emulsion system.

Transfer hydrogenation of alkenes and aldehydes

Transfer hydrogenation of alkenes catalyzed by 16-18 using amine borane as a hydrogen source

Transfer hydrogenation of alkenes in the presence of an in situ generated nickel catalyst derived from Binapine.



   |<      <<      >>     > |    

SEARCH



© 2024 chempedia.info