Davis-Beirut Reaction: Diverse Chemistries of Highly Reactive Nitroso Intermediates in Heterocycle Synthesis.
Journal
Accounts of chemical research
ISSN: 1520-4898
Titre abrégé: Acc Chem Res
Pays: United States
ID NLM: 0157313
Informations de publication
Date de publication:
20 08 2019
20 08 2019
Historique:
pubmed:
23
7
2019
medline:
7
8
2020
entrez:
23
7
2019
Statut:
ppublish
Résumé
Indazoles are an important class of nitrogen heterocycles because of their excellent performance in biologically relevant applications, such as in chemical biology and medicinal chemistry. In these applications, convenient synthesis using commercially available and diverse building blocks is highly desirable. Within this broad class, 2
Identifiants
pubmed: 31328502
doi: 10.1021/acs.accounts.9b00220
pmc: PMC6702092
mid: NIHMS1044831
doi:
Substances chimiques
Amines
0
Indazoles
0
Nitroso Compounds
0
Types de publication
Journal Article
Research Support, N.I.H., Extramural
Research Support, Non-U.S. Gov't
Review
Langues
eng
Sous-ensembles de citation
IM
Pagination
2256-2265Subventions
Organisme : NIDDK NIH HHS
ID : P30 DK072517
Pays : United States
Organisme : NIDDK NIH HHS
ID : R01 DK067003
Pays : United States
Références
Cancer. 2001 Aug 15;92(4):875-85
pubmed: 11550161
Chem Rev. 1996 Dec 19;96(8):3147-3176
pubmed: 11848856
Org Lett. 2004 Mar 4;6(5):743-6
pubmed: 14986964
J Am Chem Soc. 2004 Apr 14;126(14):4581-95
pubmed: 15070376
J Org Chem. 2005 Feb 4;70(3):1060-2
pubmed: 15675871
J Org Chem. 2006 Mar 31;71(7):2687-9
pubmed: 16555821
J Org Chem. 2006 Apr 28;71(9):3501-5
pubmed: 16626131
Chem Rev. 2006 Jul;106(7):2875-911
pubmed: 16836303
ChemMedChem. 2007 Jan;2(1):58-61
pubmed: 17154430
J Comb Chem. 2007 Jan-Feb;9(1):171-7
pubmed: 17206845
Angew Chem Int Ed Engl. 2007;46(18):3323-5
pubmed: 17385767
J Org Chem. 2008 Jan 4;73(1):234-40
pubmed: 18052193
J Med Chem. 2008 Apr 10;51(7):2137-46
pubmed: 18318468
J Med Chem. 2008 Aug 14;51(15):4632-40
pubmed: 18620382
J Med Chem. 2008 Sep 25;51(18):5522-32
pubmed: 18754654
Clin Cancer Res. 2008 Nov 15;14(22):7272-83
pubmed: 19010843
Org Lett. 2009 Jul 2;11(13):2760-3
pubmed: 19505119
Angew Chem Int Ed Engl. 2009;48(37):6879-82
pubmed: 19681082
J Med Chem. 2009 Nov 26;52(22):7170-85
pubmed: 19873981
Chem Rev. 2010 Aug 11;110(8):4489-97
pubmed: 20380420
Org Lett. 2010 Jun 4;12(11):2524-7
pubmed: 20438102
Org Lett. 2011 Mar 4;13(5):1060-3
pubmed: 21294577
Org Lett. 2011 Jun 17;13(12):3138-41
pubmed: 21612219
Org Lett. 2012 Aug 3;14(15):3870-3
pubmed: 22823414
Eur J Med Chem. 2012 Dec;58:214-27
pubmed: 23124218
Tetrahedron Lett. 2012 Nov 28;53(48):6475-6478
pubmed: 23139435
Chem Rev. 2013 Jan 9;113(1):119-91
pubmed: 23256727
Invest New Drugs. 2013 Aug;31(4):833-44
pubmed: 23275061
Org Lett. 2013 Apr 19;15(8):2062-5
pubmed: 23557405
Bioorg Med Chem Lett. 2013 May 15;23(10):2936-40
pubmed: 23582275
J Am Chem Soc. 2013 Jun 19;135(24):8802-5
pubmed: 23711098
Angew Chem Int Ed Engl. 2013 Jul 15;52(29):7509-13
pubmed: 23740864
Org Lett. 2014 Jun 6;16(11):3114-7
pubmed: 24848311
J Org Chem. 2014 Aug 1;79(15):6939-45
pubmed: 25019525
Chem Biol Drug Des. 2015 Jul;86(1):19-65
pubmed: 25352112
Bioorg Med Chem. 2014 Nov 15;22(22):6422-9
pubmed: 25438766
J Am Chem Soc. 2017 May 24;139(20):6839-6842
pubmed: 28489354
J Org Chem. 2017 Oct 20;82(20):10875-10882
pubmed: 28922917
Molecules. 2018 Jan 12;23(1):null
pubmed: 29329257
Org Lett. 2018 Mar 2;20(5):1308-1311
pubmed: 29431446
Chemistry. 2018 Jun 26;24(36):9090-9100
pubmed: 29644761
Org Lett. 2018 Aug 17;20(16):4736-4739
pubmed: 30067041
Chem Commun (Camb). 2018 Oct 2;54(79):11180-11183
pubmed: 30229253
J Org Chem. 2018 Dec 21;83(24):15493-15498
pubmed: 30468072
J Am Chem Soc. 2019 Apr 17;141(15):6247-6253
pubmed: 30912441