"Tetralones"[nm] - Search Results

Year	Number of Results
1946	1
1948	1
1949	1
1960	1
1961	1
1964	2
1972	1
1975	3
1977	1
1978	1
1980	2
1981	5
1982	7
1983	10
1984	10
1985	17
1986	17
1987	15
1988	7
1989	9
1990	13
1991	4
1992	5
1993	6
1994	8
1995	8
1996	6
1997	8
1998	5
1999	2
2000	5
2001	3
2002	1
2003	6
2004	4
2005	8
2006	12
2007	4
2008	8
2009	2
2010	14
2011	10
2012	13
2013	13
2014	10
2015	7
2016	11
2017	8
2018	8
2019	11
2020	5
2021	7
2022	4
2023	6
2024	3

1

Synthesis of new α-Aryl-α-tetralones and α-Fluoro-α-aryl-α-tetralones, preliminary antiproliferative evaluation on drug resistant cell lines and in silico prediction of ADMETox properties.

de Souza LG, Salustiano EJ, da Costa KM, Costa AT, Rumjanek VM, Domingos JLO, Rennó MN, Costa PRR. de Souza LG, et al. Bioorg Chem. 2021 May;110:104790. doi: 10.1016/j.bioorg.2021.104790. Epub 2021 Mar 4. Bioorg Chem. 2021. PMID: 33743223

2

Na₂S·9H₂O Enabled Defluorodisulfuration and Hydrodefluorination of Perfluorobutyl Tetralones: Synthesis of Trifluoromethyl 1,2-Dithioles.

Yu ZL, Feng MH, Zhang PY, Xu H, Ge D, Ma M, Shen ZL, Chu XQ. Yu ZL, et al. Org Lett. 2023 Jun 16;25(23):4388-4393. doi: 10.1021/acs.orglett.3c01573. Epub 2023 Jun 2. Org Lett. 2023. PMID: 37267202

3

Tetralones and flavonoids from Pyrola calliantha.

Liu L, Li AL, Zhao MB, Tu PF. Liu L, et al. Chem Biodivers. 2007 Dec;4(12):2932-7. doi: 10.1002/cbdv.200790242. Chem Biodivers. 2007. PMID: 18081103

4

A Convenient Diels-Alder Approach toward Potential Polyketide-like Antibiotics Using α-Activated α,β-Unsaturated 4,4-Dimethyl-1-tetralones as Dienophiles.

Lee CJ, Ramasamy M, Kuan HH, Wu CH, Lee CC, Lee JC, Shia KS. Lee CJ, et al. Molecules. 2023 Mar 17;28(6):2739. doi: 10.3390/molecules28062739. Molecules. 2023. PMID: 36985714 Free PMC article.

5

Total Synthesis of (-)-Morphine.

Umihara H, Yokoshima S, Inoue M, Fukuyama T. Umihara H, et al. Chemistry. 2017 May 23;23(29):6993-6995. doi: 10.1002/chem.201701438. Epub 2017 Apr 25. Chemistry. 2017. PMID: 28378531

6

General synthesis of 8-aryl-2-tetralones.

Carreño MC, Gonzalez-López M, Latorre A, Urbano A. Carreño MC, et al. J Org Chem. 2006 Jun 23;71(13):4956-64. doi: 10.1021/jo060688j. J Org Chem. 2006. PMID: 16776527

7

Research progress in pharmacological activities and structure-activity relationships of tetralone scaffolds as pharmacophore and fluorescent skeleton.

Sheng K, Song Y, Lei F, Zhao W, Fan L, Wu L, Liu Y, Wu S, Zhang Y. Sheng K, et al. Eur J Med Chem. 2022 Jan 5;227:113964. doi: 10.1016/j.ejmech.2021.113964. Epub 2021 Nov 1. Eur J Med Chem. 2022. PMID: 34743062 Review.

8

Synthesis of 5-Methoxy-6-isopropyl-1-tetralone.

Vera WJ, Banerjee AK. Vera WJ, et al. Nat Prod Commun. 2016 May;11(5):671-2. Nat Prod Commun. 2016. PMID: 27319147

9

CH-activating oxidative hydroxylation of 1-tetralones and related compounds with high regio- and stereoselectivity.

Roiban GD, Agudo R, Ilie A, Lonsdale R, Reetz MT. Roiban GD, et al. Chem Commun (Camb). 2014 Nov 28;50(92):14310-3. doi: 10.1039/c4cc04925j. Chem Commun (Camb). 2014. PMID: 25168091

10

An approach to (±)-Lingzhiol.

Li X, Liu X, Jiao X, Yang H, Yao Y, Xie P. Li X, et al. Org Lett. 2016 Apr 15;18(8):1944-6. doi: 10.1021/acs.orglett.6b00542. Epub 2016 Apr 4. Org Lett. 2016. PMID: 27043213

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