Synthesis of N,N '-Dialkylated Cyclohexane-1,2-diamines and Their Application as Asymmetric Ligands and Organocatalysts for the Synthesis of Alcohols

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A series of N,N'-dialkylated derivatives of (1R, 2R)-cyclohexane-1,2-diamine were synthesized, and a new approach to the one-pot preparation of this type of amine was demonstrated. The prepared diamines were used as organocatalysts for the two-step synthesis of ahydroxy gamma-keto esters from arenes, chlorooxoacetates, and ketones; they were also used as chiral ligands for Meervein-Ponndorf-Verley reductions and Henry reactions.
Publisher
GEORG THIEME VERLAG KG
Issue Date
2017-03
Language
English
Article Type
Article
Keywords

MUKAIYAMA ALDOL REACTION; ALPHA-KETO ESTERS; AMINE-IMINE CATALYST; AQUEOUS-MEDIUM; CARBON CENTER; CONSTRUCTION; WATER; PROLINEAMIDE; PROLINAMIDE; ALDEHYDES

Citation

SYNLETT, v.28, no.5, pp.615 - 619

ISSN
0936-5214
DOI
10.1055/s-0036-1588382
URI
http://hdl.handle.net/10203/224748
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