Asymmetric Hydrogenation of 3-Substituted Pyridinium Salts

The use of an equivalent amount of an organic base leads to high enantiomeric excess in the asymmetric hydrogenation of N‐benzylated 3‐substituted pyridinium salts into the corresponding piperidines. Indeed, in the presence of Et3N, a Rh‐JosiPhos catalyst reduced a range of pyridinium salts with ee...

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Vydané v:	Chemistry : a European journal Ročník 22; číslo 28; s. 9528 - 9532
Hlavní autori:	Renom-Carrasco, Marc, Gajewski, Piotr, Pignataro, Luca, de Vries, Johannes G., Piarulli, Umberto, Gennari, Cesare, Lefort, Laurent
Médium:	Journal Article
Jazyk:	English
Vydavateľské údaje:	WEINHEIM Blackwell Publishing Ltd 04.07.2016 Wiley Wiley Subscription Services, Inc
Predmet:	asymmetric catalysis Asymmetry Chemistry Chemistry, Multidisciplinary Equivalence homogeneous catalysis Hydrogenation Isotopic labeling Labyrinth Pathways Physical Sciences Piperidine Pyridines reaction mechanisms Salts Science & Technology SCOPE MONODENTATE PHOSPHORAMIDITE LIGANDS reaction mechanisms QUINOLINES asymmetric catalysis DEHYDROAMINO ACID-DERIVATIVES hydrogenation MULTIPLE STEREOGENIC CENTERS IRIDIUM-CATALYZED HYDROGENATION HIGHLY ENANTIOSELECTIVE HYDROGENATION pyridines homogeneous catalysis REDUCTION PIPERIDINES ISOQUINOLINIUM SALTS
ISSN:	0947-6539, 1521-3765, 1521-3765
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