Asymmetric direct Aldol reaction between acetone and aromatic aldehydes catalyzed by diazadioxocalix[2]arene[2]triazine derivatives

被引:0
|
作者
Ozgun, Ummu [1 ,2 ]
Sirit, Abdulkadir [3 ]
Genc, Hayriye Nevin [4 ]
机构
[1] Necmettin Erbakan Univ, AK Educ Fac, Dept Chem, TR-42090 Konya, Turkiye
[2] Necmettin Erbakan Univ, Fac Engn, Dept Mechatron Engn, TR-42090 Konya, Turkiye
[3] Necmettin Erbakan Univ, AK Educ Fac, Dept Chem Educ, TR-42090 Konya, Turkiye
[4] Necmettin Erbakan Univ, AK Educ Fac, Dept Sci Educ, TR-42090 Konya, Turkiye
关键词
Asymmetric synthesis; Aldol reaction; Organocatalysis; Stereoselectivity; CHIRAL ORGANOCATALYSTS; PI INTERACTIONS; CAGE;
D O I
10.1007/s10847-024-01260-2
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Novel derivatives of diazadioxocalix[2]arene[2]triazine were synthesized and evaluated for their catalytic effects on direct asymmetric Aldol reactions in organic solvents. Chiral groups were attached to the heteroatom-bridged calix[2]triazine scaffold through reactions involving (R)/(S)-1,2,3,4-tetrahydro-1-naphthylamine with diazadioxocalix[2]arene[2]triazine. Diazadioxocalix[2]arene[2]triazine derivatives were found to be effective catalysts for the reaction of acetone with aromatic aldehydes. According to the obtained results, it has been determined that the moiety of the catalyst affects the configuration of the Aldol product. The Aldol adducts were obtained in excellent yields (93%) and enantioselectivities (96%).
引用
收藏
页码:623 / 632
页数:10
相关论文
共 50 条
  • [21] Proline-catalyzed aldol reaction of acetone with (R)- and (S)-2,3-O-alkylideneglyceraldehydes
    Yu. Yu. Kozhemyakin
    Yu. Yu. Kozyrkov
    Russian Journal of Organic Chemistry, 2015, 51 : 566 - 568
  • [22] Proline-catalyzed aldol reaction of acetone with (R)- and (S)-2,3-O-alkylideneglyceraldehydes
    Kozhemyakin, Yu. Yu.
    Kozyrkov, Yu. Yu.
    RUSSIAN JOURNAL OF ORGANIC CHEMISTRY, 2015, 51 (04) : 566 - 568
  • [23] Design, Synthesis and Organocatalysis of 2,2′-Biphenol-Based Prolinamide Organocatalysts in the Asymmetric Direct Aldol Reaction in Water
    Zhao, Hong-Wu
    Sheng, Zhi-Hui
    Meng, Wei
    Yue, Yuan-Yuan
    Li, Hai-Long
    Song, Xiu-Qing
    Yang, Zhao
    SYNLETT, 2013, 24 (20) : 2743 - 2747
  • [24] Asymmetric tandem Michael-aldol reactions between 3-cinnamoyloxazolidine-2-thiones and aldehydes
    Kinoshita, Hironori
    Osamura, Takashi
    Mizuno, Kazumi
    Kinoshita, Sayaka
    Iwamura, Tatsunori
    Watanabe, Shin-ichi
    Kataoka, Tadashi
    Muraoka, Osamu
    Tanabe, Genzoh
    CHEMISTRY-A EUROPEAN JOURNAL, 2006, 12 (14) : 3896 - 3904
  • [25] Asymmetric Direct Aldol Reaction Catalyzed by (1R, 2R)-(+)-1, 2-Diammonium Cyclohexane-L-tartrate in Water
    Mondal, Anirban
    Bhowmick, Kartick Chandra
    CURRENT ORGANOCATALYSIS, 2019, 6 (02) : 165 - 170
  • [26] Asymmetric Synthesis of Trisubstituted Oxazolidinones by the Thiourea-Catalyzed Aldol Reaction of 2-Isocyanatomalonate Diester
    Sakamoto, Shota
    Kazumi, Naoya
    Kobayashi, Yusuke
    Tsukano, Chihiro
    Takemoto, Yoshiji
    ORGANIC LETTERS, 2014, 16 (18) : 4758 - 4761
  • [27] Asymmetric Synthesis of Spirooxazolidinone Oxindoles by the Thiourea-Catalyzed Aldol Reaction of 2-Isocyanatomalonate Diesters
    Chen, Xiao-Pan
    Liu, Jin-Xin
    Li, Hong-Yan
    Xiao, You-Cai
    Chen, Fen-Er
    ADVANCED SYNTHESIS & CATALYSIS, 2022, 364 (12) : 2067 - 2071
  • [28] Asymmetric Aldol Reaction of 3-Acetyl-2H-chromen-2-ones and Isatins Catalyzed by a Bifunctional Quinidine Urea Catalyst
    Abbaraju, Santhi
    Zhao, John Cong-Gui
    ADVANCED SYNTHESIS & CATALYSIS, 2014, 356 (01) : 237 - 241
  • [29] Acyclic Amino Acids Catalyzed Direct Asymmetric Aldol Reactions in Aqueous Media Assisted by 2,4-Dinitrophenol
    Deng, Dongsheng
    Liu, Ping
    Ji, Baoming
    Fu, Weijun
    Li, Long
    CATALYSIS LETTERS, 2010, 137 (3-4) : 163 - 170
  • [30] Direct Catalytic Asymmetric Synthesis of Highly Functionalized 2-Methylchroman-2,4-diols via Barbas-List Aldol Reaction
    Ramachary, Dhevalapally B.
    Sakthidevi, Rajasekar
    CHEMISTRY-A EUROPEAN JOURNAL, 2009, 15 (18) : 4516 - 4522