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Third‐Generation Amino Acid Furanoside‐Based Ligands from d ‐Mannose for the Asymmetric Transfer Hydrogenation of Ketones: Catalysts with an Exceptionally Wide Substrate Scope
Author(s) -
Margalef Jèssica,
Slagbrand Tove,
Tinnis Fredrik,
Adolfsson Hans,
Diéguez Montserrat,
Pàmies Oscar
Publication year - 2016
Publication title -
advanced synthesis and catalysis
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.541
H-Index - 155
eISSN - 1615-4169
pISSN - 1615-4150
DOI - 10.1002/adsc.201600903
Subject(s) - chemistry , transfer hydrogenation , ruthenium , catalysis , aryl , alkyl , organic chemistry , allylic rearrangement , noyori asymmetric hydrogenation , ketone , rhodium , ligand (biochemistry) , acetophenone , asymmetric hydrogenation , combinatorial chemistry , enantioselective synthesis , medicinal chemistry , biochemistry , receptor
A modular ligand library of α‐amino acid hydroxyamides and thioamides was prepared from 10 different N‐ tert ‐butyloxycarbonyl‐protected α‐amino acids and three different amino alcohols derived from 2,3‐ O ‐isopropylidene‐α‐ d ‐mannofuranoside. The ligand library was evaluated in the half‐sandwich ruthenium‐ and rhodium‐catalyzed asymmetric transfer hydrogenation of a wide array of ketone substrates, including simple as well as sterically demanding aryl alkyl ketones, aryl fluoroalkyl ketones, heteroaromatic alkyl ketones, aliphatic, conjugated and propargylic ketones. Under the optimized reaction conditions, secondary alcohols were obtained in high yields and in enantioselectivities up to >99%. The choice of ligand/catalyst allowed for the generation of both enantiomers of the secondary alcohols, where the ruthenium‐hydroxyamide and the rhodium‐thioamide catalysts act complementarily towards each other. The catalytic systems were also evaluated in the tandem isomerization/asymmetric transfer hydrogenation of racemic allylic alcohols to yield enantiomerically enriched saturated secondary alcohols in up to 98% ee . Furthermore, the catalytic tandem α‐alkylation/asymmetric transfer hydrogenation of acetophenones and 3‐acetylpyridine with primary alcohols as alkylating and reducing agents was studied. Secondary alcohols containing an elongated alkyl chain were obtained in up to 92% ee .