Design, synthesis and structure determination of new inherently chiral para-bromoalkoxycalix[4]arenes

被引:4
|
作者
Yesypenko, Oleksandr A. [1 ]
Klyachina, Marija A. [1 ]
Dekhtyarenko, Maksym V. [2 ]
Pirozhenko, Vladimir V. [1 ]
Shishkina, Svitlana V. [3 ,4 ]
Boyko, Vyacheslav I. [1 ]
Voitenko, Zoia V. [2 ]
Kalchenko, Vitaly I. [1 ]
机构
[1] Natl Acad Sci Ukraine, Inst Organ Chem, Kiev, Ukraine
[2] Kiev Natl Taras Shevchenko Univ, Dept Chem, Kiev, Ukraine
[3] Natl Acad Sci Ukraine, STC Inst Single Crystals, Kharkov, Ukraine
[4] Kharkov Natl Univ, Dept Inorgan Chem, Kharkov, Ukraine
关键词
Inherently chiral calix[4]arenes; stereoselective synthesis; diastereomers; enantiomers; optical resolution; OPTICAL RESOLUTION; ENANTIOSELECTIVE RECOGNITION; RIM; SUBSTITUENTS; CALIXARENES; ACIDS;
D O I
10.1080/10610278.2016.1167210
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
The preparative method for the synthesis of inherently chiral para-bromoalkoxycalix[4]arenes based on para-bromination, stepwise regioselective debenzoylation and the following alkylation of the readily available 25-propoxy-26,27-dibenzoyloxycalix[4]arene with propyl bromide or (R)-N-(1-phenylethyl)bromoacetamide has been developed. Three types of the inherently chiral calix[4] arenes in cone or partial cone conformations with asymmetrical ((HBHH)(AHHH), (HBHH)(AAHH), (HCHH)(AHBH)) substitution of both upper and lower rims have been obtained in racemic, diastereomerically pure or enantiomerically pure forms. Their structure and the absolute configuration have been determined by NMR and X-ray. [GRAPHICS] .
引用
收藏
页码:49 / 58
页数:10
相关论文
共 50 条
  • [21] Cavity-extended inherently chiral resorein[4]arenes: Synthesis and chiroptical properties of the cycloenantiomers
    Paletta, Marlene
    Klaes, Michael
    Neumann, Beate
    Stammler, Hans-Georg
    Grimme, Stefan
    Mattay, Jochen
    EUROPEAN JOURNAL OF ORGANIC CHEMISTRY, 2008, 2008 (03) : 555 - 562
  • [22] 3-Methylcalix[4]arene: A new versatile precursor to inherently chiral calix[4]arenes
    Fu, DK
    Xu, B
    Swager, TM
    JOURNAL OF ORGANIC CHEMISTRY, 1996, 61 (02): : 802 - 804
  • [23] Synthesis and characterization of new chiral calix[4]arenes
    Okada, Y
    Mizutani, M
    Nishimura, J
    ENANTIOMER, 2002, 7 (2-3): : 93 - 106
  • [24] A new approach to enantiopure inherently chiral calix[4]arenes: Determination of their absolute configurations (vol 72, pg 4448, 2007)
    Xu, Zhen-Xiang
    Zhang, Chun
    Zheng, Qi-Yu
    Chen, Chuan-Feng
    Huang, Zhi-Tang
    ORGANIC LETTERS, 2007, 9 (25) : 5331 - 5331
  • [25] Resolution of inherently chiral anti-O,O′-dialkylthiacalix[4]arenes and determination of their absolute stereochemistries
    Narumi, Fumitaka
    Matsumura, Nobuji
    Sasagawa, Nariaki
    Natori, Koichi
    Kajiwara, Takashi
    Hattori, Tetsutaro
    TETRAHEDRON-ASYMMETRY, 2008, 19 (12) : 1470 - 1475
  • [26] Ketone transformation as a pathway to inherently chiral rigidified calix[4]arenes
    Tlusty, Martin
    Spalovska, Dita
    Kohout, Michal
    Eigner, Vaclav
    Lhotak, Pavel
    CHEMICAL COMMUNICATIONS, 2020, 56 (84) : 12773 - 12776
  • [27] Synthesis of enantiomerically pure inherently chiral calix[4]arenes using the meta-substitution strategy
    Tlusty, Martin
    Spalovska, Dita
    Babor, Martin
    Lhotak, Pavel
    TETRAHEDRON LETTERS, 2019, 60 (03) : 260 - 263
  • [28] Catalytic Asymmetric Synthesis of Inherently Chiral Calix[4]arenes via Sequential Povarov Reaction and Aromatizations
    Li, Wan
    Shi, Feng
    CHINESE JOURNAL OF ORGANIC CHEMISTRY, 2024, 44 (10) : 3265 - 3267
  • [29] Catalytic Enantioselective Synthesis of Inherently Chiral Calix[4]arenes via Sequential Povarov Reaction and Aromatizations
    Yu, Shaoze
    Yuan, Mengyao
    Xie, Wansen
    Ye, Zidan
    Qin, Tianren
    Yu, Na
    Yang, Xiaoyu
    ANGEWANDTE CHEMIE-INTERNATIONAL EDITION, 2024, 63 (45)
  • [30] First synthesis, isolation and complete characterization of both enantiomers of inherently chiral resorc[4]arenes by monofunctionalization
    Agena, C
    Wolff, C
    Mattay, J
    EUROPEAN JOURNAL OF ORGANIC CHEMISTRY, 2001, 2001 (15) : 2977 - 2981