Selected applications of Meldrum's acid - a tutorial

被引:27
|
作者
Brosge, Felix [1 ]
Singh, Pardeep [1 ]
Almqvist, Fredrik [1 ]
Bolm, Carsten [1 ]
机构
[1] Rhein Westfal TH Aachen, Inst Organ Chem, Landoltweg 1, D-52074 Aachen, Germany
关键词
STEREOSELECTIVE-SYNTHESIS; MULTICOMPONENT SYNTHESIS; GAMMA-BUTYROLACTONES; CYCLOADDITION; FUNCTIONALIZATION; NITROSOKETENE; QUATERNARY; PYROLYSIS; ARYLATION; ESTERS;
D O I
10.1039/d1ob00395j
中图分类号
O62 [有机化学];
学科分类号
070303 ; 081704 ;
摘要
Due to its unique structure and the vast array of substituents that can be attached to its core, Meldrum's acid is a molecule with exceptional chemical properties. In water, it has a remarkably low pK(a) value of about 4.9. Its C5 position is readily involved in electrophilic substitution reactions whereas the C4 and C6 positions are easily attacked by nucleophiles. At elevated temperatures Meldrum's acid undergoes distinctive decomposition pathways, which can be used in cycloaddition and acylation reactions. In this Tutorial Review, the authors intend to introduce the principles of the synthetic chemistry of Meldrum's acid and provide the essential knowledge for the design and preparation of compounds with desired properties. As there are many reviews focusing on a specific detail of Meldrum's acid chemistry, we would like to give a broader picture of this diverse molecule for undergraduate and graduate students as well as experienced lab leaders. For achieving this goal, some recent advances in using Meldrum's acid derivatives in synthetic scenarios are presented with the hope to further stimulate and promote research leading to additional innovative applications of this synthetically highly relevant molecule.
引用
收藏
页码:5014 / 5027
页数:14
相关论文
共 50 条
  • [1] Synthetic applications of the pyrolysis of Meldrum's acid derivatives
    Gaber, AAM
    McNab, H
    SYNTHESIS-STUTTGART, 2001, (14): : 2059 - 2074
  • [2] Synthetic applications of the pyrolysis of Meldrum's acid derivatives
    Gaber, A.E.-A.M.
    McNab, H.
    Synthesis, 2001, (14) : 2059 - 2074
  • [3] Meldrum's acid
    Bonifácio, VDB
    SYNLETT, 2004, (09) : 1649 - 1650
  • [4] Meldrum's acid
    Kidd, Hamish
    CHEMISTRY WORLD, 2008, 5 (11): : 35 - 36
  • [5] Acid-catalyzed breakdown of alkoxide and thiolate ion adducts of benzylidene Meldrum's acid, methoxybenzylidene Meldrum's acid and thiomethoxybenzylidene Meldrum's acid
    Bernasconi, CF
    Ketner, RJ
    Brown, SD
    Chen, X
    Rappoport, Z
    JOURNAL OF ORGANIC CHEMISTRY, 1999, 64 (24): : 8829 - 8839
  • [6] Acylation studies with Meldrum's acid
    Mahulikar, PP
    Mane, RB
    SYNTHETIC COMMUNICATIONS, 2005, 35 (16) : 2139 - 2141
  • [7] Meldrum's acid in multicomponent reactions:: Applications to combinatorial and diversity-oriented synthesis
    Gerencsér, J
    Dormán, G
    Darvas, F
    QSAR & COMBINATORIAL SCIENCE, 2006, 25 (5-6): : 439 - 448
  • [8] Two methylsulfanylmethylene derivatives of Meldrum's acid
    Gould, RO
    Harris, SG
    McNab, H
    Parsons, S
    Withell, K
    ACTA CRYSTALLOGRAPHICA SECTION C-CRYSTAL STRUCTURE COMMUNICATIONS, 1998, 54 : 234 - 236
  • [9] Two methylsulfanylmethylene derivatives of Meldrum's acid
    Gould, R.O.
    Harris, S.G.
    McNab, H.
    Parsons, S.
    Withell, K.
    Acta Crystallographica, Section C: Crystal Structure Communications, 1998, 54 (pt 2): : 234 - 236
  • [10] Synthesis of triketones from Meldrum's acid
    Skuratova, MI
    Fedotova, OV
    Kharchenko, VG
    RUSSIAN JOURNAL OF ORGANIC CHEMISTRY, 2002, 38 (09) : 1380 - 1381