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

被引:5
|
作者
Tsygankov, Alexey A. [1 ]
Chun, Man-Seog [2 ]
Samoylova, Alexandra D. [1 ]
Kwon, Seongyeon [2 ]
Kreschenova, Yuliya M. [1 ]
Kim, Suhyeon [2 ]
Shin, Euijin [2 ]
Oh, Jinho [2 ]
Strelkova, Tatyana V. [3 ]
Kolesov, Valerii S. [3 ]
Zubkov, Fedor I. [4 ]
Semenov, Sergei E. [1 ]
Fedyanin, Ivan V. [3 ]
Chusov, Denis [1 ,3 ,4 ]
机构
[1] Moscow Chem Lyceum, Tamozhenniy Proezd 4, Moscow, Russia
[2] Korea Adv Inst Sci & Technol, Korea Sci Acad, 105-47 Baegyanggwanmun Ro, Busan 47162, South Korea
[3] Russian Acad Sci, AN Nesmeyanov Inst Organoelement Cpds, Vavilova Str 28, Moscow 119991, Russia
[4] Peoples Friendship Univ Russia, Dept Organ Chem, 6 Miklukho Maklaya St, Moscow 117198, Russia
基金
俄罗斯科学基金会;
关键词
aldol reaction; organocatalysis; asymmetric catalysis; hydroxy acids; diamines; Meervein-Ponndorf-Verley reaction; Henry reaction; MUKAIYAMA ALDOL REACTION; ALPHA-KETO ESTERS; AMINE-IMINE CATALYST; AQUEOUS-MEDIUM; CARBON CENTER; CONSTRUCTION; WATER; PROLINEAMIDE; PROLINAMIDE; ALDEHYDES;
D O I
10.1055/s-0036-1588382
中图分类号
O62 [有机化学];
学科分类号
070303 ; 081704 ;
摘要
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.
引用
收藏
页码:615 / 619
页数:5
相关论文
共 50 条
  • [1] Application of phosphorylated reagents derived from N,N′-di-[(S)-α-phenylethyl]-cyclohexane-1,2-diamines in the determination of the enantiomeric purity of chiral alcohols
    de Parrodi, CA
    Moreno, GE
    Quintero, L
    Juaristi, E
    TETRAHEDRON-ASYMMETRY, 1998, 9 (12) : 2093 - 2099
  • [2] Preparation of Chiral Photosensitive Organocatalysts and Their Application for the Enantioselective Synthesis of 1,2-Diamines
    Lyu, Jiyuan
    Claraz, Aurelie
    Vitale, Maxime R.
    Allain, Clemence
    Masson, Geraldine
    JOURNAL OF ORGANIC CHEMISTRY, 2020, 85 (20): : 12843 - 12855
  • [3] An efficient method for the synthesis of N,N'-dimethyl-1,2-diamines
    Tye, H
    Eldred, C
    Wills, M
    TETRAHEDRON LETTERS, 2002, 43 (01) : 155 - 158
  • [4] Catalytic asymmetric synthesis of 1,2-diamines
    Foubelo, Francisco
    Najera, Carmen
    Retamosa, Ma Gracia
    Sansano, Jose M.
    Yus, Miguel
    CHEMICAL SOCIETY REVIEWS, 2024, 53 (15) : 7983 - 8085
  • [5] Asymmetric Henry reactions of aldehydes with various nitroalkanes catalyzed by copper(II) complexes of novel chiral N-monoalkyl cyclohexane-1,2-diamines
    Liu, Fei
    Gou, Shaohua
    Li, Lei
    APPLIED ORGANOMETALLIC CHEMISTRY, 2014, 28 (03) : 186 - 193
  • [6] Construction of Quaternary Stereocenters: Asymmetric α-Amination of Branched Aldehydes Catalyzed by Monoimide Substituted Cyclohexane-1,2-Diamines
    Fu, Ji-Ya
    Wang, Qi-Lin
    Peng, Lin
    Gui, Yong-Yuan
    Xu, Xiao-Ying
    Wang, Li-Xin
    CHIRALITY, 2013, 25 (10) : 668 - 672
  • [7] Synthesis of oxazolidinones and 1,2-diamines from N-alkyl aziridines
    Hancock, MT
    Pinhas, AR
    SYNTHESIS-STUTTGART, 2004, (14): : 2347 - 2355
  • [8] Asymmetric synthesis of β-amino alcohols and 1,2-diamines through DuPHOS-Rh catalysed hydrogenation
    Burk, MJ
    Johnson, NB
    Lee, JR
    TETRAHEDRON LETTERS, 1999, 40 (36) : 6685 - 6688
  • [9] New Heterodinuclear Zn/Ln (Ln = Gd, Tb, Er, Yb) Complexes of Hexadentate N,N′-Bis(3-alkoxy-2-hydroxybenzyl)cyclohexane-1,2-diamines: Synthesis and Structure
    Kelly, Norman
    Schnaars, Kathleen
    Gloe, Kerstin
    Doert, Thomas
    Weigand, Jan J.
    Gloe, Karsten
    AUSTRALIAN JOURNAL OF CHEMISTRY, 2017, 70 (05) : 601 - 607
  • [10] Synthesis of chiral 1,2-diamines by asymmetric lithiation-substitution
    Coldham, I
    Copley, RCB
    Haxell, TFN
    Howard, S
    ORGANIC LETTERS, 2001, 3 (23) : 3799 - 3801