Recyclization of Maleimides by Binucleophiles as a General Approach for Building Hydrogenated Heterocyclic Systems.

N-arylmaleimides hydrogenated heterocyclic compounds recyclization

Journal

Molecules (Basel, Switzerland)
ISSN: 1420-3049
Titre abrégé: Molecules
Pays: Switzerland
ID NLM: 100964009

Informations de publication

Date de publication:
18 Aug 2022
Historique:
received: 01 06 2022
revised: 12 08 2022
accepted: 16 08 2022
entrez: 26 8 2022
pubmed: 27 8 2022
medline: 30 8 2022
Statut: epublish

Résumé

The building of heterocyclic systems containing hydrogenated fragments is an important step towards the creation of biologically-active compounds with a wide spectrum of pharmacological activity. Among the numerous methods for creating such systems, a special place is occupied by processes using

Identifiants

pubmed: 36014507
pii: molecules27165268
doi: 10.3390/molecules27165268
pmc: PMC9416709
pii:
doi:

Substances chimiques

Maleimides 0

Types de publication

Journal Article Review

Langues

eng

Sous-ensembles de citation

IM

Subventions

Organisme : Russian Science Foundation
ID : 18-74-10097

Références

J Med Chem. 1990 Oct;33(10):2870-5
pubmed: 2213839
Pharmacol Biochem Behav. 2011 Apr;98(2):227-33
pubmed: 21215770
ACS Med Chem Lett. 2018 Dec 18;10(1):98-104
pubmed: 30655954
J Med Chem. 1987 Apr;30(4):623-7
pubmed: 3031290
PLoS One. 2014 Jan 23;9(1):e86806
pubmed: 24466249
Eur J Med Chem. 2007 May;42(5):641-8
pubmed: 17303290
J Med Chem. 2008 Jul 10;51(13):3661-80
pubmed: 18457385
J Med Chem. 2020 Dec 24;63(24):15564-15590
pubmed: 33306391
J Med Chem. 1974 Mar;17(3):273-81
pubmed: 4204335
Biochem Biophys Res Commun. 2018 Sep 10;503(3):1291-1297
pubmed: 30017191
Chem Pharm Bull (Tokyo). 1967 Nov;15(11):1738-43
pubmed: 5583832
Pharmaceuticals (Basel). 2012 Oct 23;5(10):1128-46
pubmed: 24281261
J Med Chem. 1989 Feb;32(2):342-50
pubmed: 2536438
Org Lett. 2006 Jul 6;8(14):3085-8
pubmed: 16805558
Bioorg Med Chem Lett. 2004 Nov 15;14(22):5689-92
pubmed: 15482949
Antimicrob Agents Chemother. 2001 Dec;45(12):3657-9
pubmed: 11709364
ACS Med Chem Lett. 2014 Aug 13;5(9):952-3
pubmed: 25221648
Med Res Rev. 1989 Apr-Jun;9(2):123-80
pubmed: 2654521
Bioorg Med Chem Lett. 2005 Sep 15;15(18):4023-8
pubmed: 16005624
Bioorg Med Chem Lett. 2019 Sep 15;29(18):2551-2558
pubmed: 31420269
Phytochemistry. 2008 Sep;69(12):2363-6
pubmed: 18649901
J Med Chem. 2002 Nov 7;45(23):4954-7
pubmed: 12408705
Food Chem. 2014;152:415-22
pubmed: 24444956
Eur J Med Chem. 2003 Jul-Aug;38(7-8):719-28
pubmed: 12932903
Bioorg Med Chem. 2003 Feb 20;11(4):515-20
pubmed: 12538016
Arzneimittelforschung. 2011;61(2):92-7
pubmed: 21428243
Oncotarget. 2014 May 15;5(9):2404-17
pubmed: 24811221
Chem Pharm Bull (Tokyo). 1992 May;40(5):1170-6
pubmed: 1394630
Indian J Pharm Sci. 2009 Jul;71(4):428-32
pubmed: 20502549
J Med Chem. 2018 Feb 8;61(3):1086-1097
pubmed: 29300474
Beilstein J Org Chem. 2012;8:1804-13
pubmed: 23209515
Methods Enzymol. 2011;493:509-31
pubmed: 21371604
Bioorg Med Chem Lett. 2006 May 15;16(10):2773-6
pubmed: 16495053
Drug Discov Today. 2009 Nov;14(21-22):1011-20
pubmed: 19729075
Bioorg Med Chem. 2002 May;10(5):1275-80
pubmed: 11886790
Bioorg Med Chem. 2008 May 15;16(10):5547-56
pubmed: 18430576
J Med Chem. 2009 Nov 12;52(21):6752-6
pubmed: 19827778
Nat Chem. 2009 Jun;1(3):187-92
pubmed: 21378847
Nature. 2011 Feb 3;470(7332):42-3
pubmed: 21293363
Bioorg Med Chem Lett. 2006 Mar 1;16(5):1146-50
pubmed: 16368234
Arch Pharm (Weinheim). 2014 Mar;347(3):221-8
pubmed: 24395622
J Med Chem. 2000 Oct 5;43(20):3632-40
pubmed: 11020277
J Comb Chem. 2008 May-Jun;10(3):456-9
pubmed: 18338857
J Med Chem. 1996 Apr 26;39(9):1898-906
pubmed: 8627613
Angew Chem Int Ed Engl. 2016 Jan 11;55(2):488-92
pubmed: 26526786
Beilstein J Org Chem. 2016 Nov 29;12:2563-2569
pubmed: 28144325
Curr Opin Chem Biol. 2011 Aug;15(4):469-74
pubmed: 21411360
J Asian Nat Prod Res. 2022 Jan;24(1):1-14
pubmed: 33511872
Chem Biol Drug Des. 2019 Sep;94(5):1919-1929
pubmed: 31169963
Mikrobiologiia. 2008 Sep-Oct;77(5):617-22
pubmed: 19004342
Med Chem Res. 2013 Aug;22(8):3629-3639
pubmed: 23807823
J Med Chem. 1995 Jul 21;38(15):2830-41
pubmed: 7636844
Biochemistry. 2013 Jul 2;52(26):4474-81
pubmed: 23746300
Chem Biol Drug Des. 2015 Oct;86(4):568-77
pubmed: 25600073
Angew Chem Int Ed Engl. 2007;46(35):6703-5
pubmed: 17663493
RSC Adv. 2019 Mar 5;9(13):7218-7227
pubmed: 35519992
J Med Chem. 2005 Jun 2;48(11):3816-22
pubmed: 15916433
Drug Discov Today. 2013 Dec;18(23-24):1221-7
pubmed: 23906694
Angew Chem Int Ed Engl. 2007;46(28):5352-5
pubmed: 17568465
Eur J Med Chem. 2016 Aug 8;118:259-65
pubmed: 27131068
Chem Commun (Camb). 2011 Mar 21;47(11):3219-21
pubmed: 21318205
J Med Chem. 2016 Sep 22;59(18):8189-206
pubmed: 27124799
Angew Chem Int Ed Engl. 2003 Jan 20;42(3):355-7
pubmed: 12548698
Mutat Res. 1984 May;136(2):153-7
pubmed: 6717481
Med Res Rev. 1989 Jul-Sep;9(3):291-324
pubmed: 2666803
Top Curr Chem. 2012;317:1-32
pubmed: 21695633
Bioorg Med Chem. 2008 Mar 1;16(5):2156-70
pubmed: 18248994
J Med Chem. 1983 Jun;26(6):800-7
pubmed: 6854582
Bioorg Med Chem. 2018 Jul 15;26(11):2996-3005
pubmed: 29779669
J Med Chem. 1996 Jan 5;39(1):297-303
pubmed: 8568820
Eur J Med Chem. 2000 Dec;35(12):1043-52
pubmed: 11248403
Bioorg Med Chem. 2007 Sep 1;15(17):5888-904
pubmed: 17561405
J Cardiovasc Pharmacol. 2016 Mar;67(3):246-51
pubmed: 26566152
J Med Chem. 1988 Feb;31(2):352-6
pubmed: 2892935
Proc Natl Acad Sci U S A. 2011 Apr 26;108(17):6799-804
pubmed: 21482811
J Med Chem. 2003 Jan 30;46(3):349-52
pubmed: 12540232
Pharmacol Rep. 2013;65(2):505-12
pubmed: 23744435

Auteurs

Dmitriy Yu Vandyshev (DY)

Department of Organic Chemistry, Faculty of Chemistry, Voronezh State University, Universitetskaya Sq. 1, 394018 Voronezh, Russia.

Khidmet S Shikhaliev (KS)

Department of Organic Chemistry, Faculty of Chemistry, Voronezh State University, Universitetskaya Sq. 1, 394018 Voronezh, Russia.
TekhnoKhim, 50 Let Sovetskoi Vlasti Str. 8, 394050 Voronezh, Russia.

Articles similaires

Divergent syntheses of complex Veratrum alkaloids.

Yinliang Guo, Runting Fang, Yang Jiao et al.
1.00
Stereoisomerism Veratrum Alkaloids Oxidation-Reduction Cyclization Cycloaddition Reaction

Conjugation of CRAMP

Sankar Rathinam, Kasper K Sørensen, Martha Á Hjálmarsdóttir et al.
1.00
Chitosan Anti-Bacterial Agents Copper Cycloaddition Reaction Azides
Animals Female Glycogen Synthase Kinase 3 beta Mice Theca Cells
Klebsiella pneumoniae Escherichia coli Liposomes Polyethylene Glycols Maleimides

Classifications MeSH