Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation

Search Page

Filters

My NCBI Filters

Results by year

Table representation of search results timeline featuring number of search results per year.

Year Number of Results
1950 2
1951 8
1952 3
1953 3
1954 2
1955 2
1956 1
1957 1
1958 2
1960 1
1961 5
1962 5
1963 6
1964 11
1965 5
1966 10
1967 20
1968 21
1969 21
1970 31
1971 29
1972 30
1973 19
1974 37
1975 39
1976 30
1977 28
1978 38
1979 45
1980 49
1981 68
1982 58
1983 72
1984 78
1985 84
1986 78
1987 90
1988 90
1989 83
1990 89
1991 108
1992 113
1993 116
1994 117
1995 129
1996 147
1997 135
1998 100
1999 131
2000 129
2001 122
2002 137
2003 128
2004 116
2005 144
2006 157
2007 159
2008 147
2009 158
2010 146
2011 154
2012 168
2013 144
2014 149
2015 120
2016 129
2017 124
2018 127
2019 124
2020 139
2021 105
2022 103
2023 80
2024 42

Text availability

Article attribute

Article type

Publication date

Search Results

5,311 results

Results by year

Filters applied: . Clear all
Page 1
Showing results for amine suzuki
Search for Amane Suzuki instead (3 results)
Aminative Suzuki-Miyaura coupling.
Onnuch P, Ramagonolla K, Liu RY. Onnuch P, et al. Science. 2024 Mar;383(6686):1019-1024. doi: 10.1126/science.adl5359. Epub 2024 Feb 29. Science. 2024. PMID: 38422125
The Suzuki-Miyaura and Buchwald-Hartwig coupling reactions are widely used to form carbon-carbon (C-C) and carbon-nitrogen (C-N) bonds, respectively. We report the incorporation of a formal nitrene insertion process into the Suzuki-Miyaura reaction, altering the pro …
The Suzuki-Miyaura and Buchwald-Hartwig coupling reactions are widely used to form carbon-carbon (C-C) and carbon-nitrogen (C-N) bond …
Groebke-Blackburn-Bienaymé Reaction for DNA-Encoded Library Technology.
An Y, Lee J, Seo H, Bae S, Kang J, Lee J, Kim J, Nam MH, Song M, Hwang GT. An Y, et al. Org Lett. 2023 Jun 23;25(24):4445-4450. doi: 10.1021/acs.orglett.3c01366. Epub 2023 Jun 13. Org Lett. 2023. PMID: 37310879
This study presents a DNA-compatible synthesis of diverse 5-arylimidazo[1,2-a]pyridin-3-amine derivatives using the Suzuki-Miyaura reaction, followed by a Groebke-Blackburn-Bienayme (GBB) reaction. ...
This study presents a DNA-compatible synthesis of diverse 5-arylimidazo[1,2-a]pyridin-3-amine derivatives using the Suzuki-Miy …
Electrochemically Enabled, Nickel-Catalyzed Amination.
Li C, Kawamata Y, Nakamura H, Vantourout JC, Liu Z, Hou Q, Bao D, Starr JT, Chen J, Yan M, Baran PS. Li C, et al. Angew Chem Int Ed Engl. 2017 Oct 9;56(42):13088-13093. doi: 10.1002/anie.201707906. Epub 2017 Sep 14. Angew Chem Int Ed Engl. 2017. PMID: 28834098 Free PMC article.
Along with amide bond formation, Suzuki cross-coupling, and reductive amination, the Buchwald-Hartwig-Ullmann-type amination of aryl halides stands as one of the most employed reactions in modern medicinal chemistry. ...Of note is the scalability, functional- …
Along with amide bond formation, Suzuki cross-coupling, and reductive amination, the Buchwald-Hartwig-Ullmann-type aminatio …
N-(3,4-dimethoxyphenethyl)-6-methyl-2,3,4,9-tetrahydro-1H-carbazol-1-amine inhibits bladder cancer progression by suppressing YAP1/TAZ.
Shiraishi Y, Maehama T, Nishio M, Otani J, Hikasa H, Mak TW, Sasaki T, Honma T, Kondoh Y, Osada H, Yoshida M, Fujisawa M, Suzuki A. Shiraishi Y, et al. Genes Cells. 2022 Oct;27(10):602-612. doi: 10.1111/gtc.12979. Epub 2022 Aug 22. Genes Cells. 2022. PMID: 36054428 Free article.
Accessing data from our previous screening of a chemical library of compounds targeting the Hippo pathway, we identified DMPCA (N-(3,4-dimethoxyphenethyl)-6-methyl-2,3,4,9-tetrahydro-1H-carbazol-1-amine) as an agent able to induce the phosphorylation of LATS1 and YAP1/TAZ …
Accessing data from our previous screening of a chemical library of compounds targeting the Hippo pathway, we identified DMPCA (N-(3,4-dimet …
Stereoconvergent amine-directed alkyl-alkyl Suzuki reactions of unactivated secondary alkyl chlorides.
Lu Z, Wilsily A, Fu GC. Lu Z, et al. J Am Chem Soc. 2011 Jun 1;133(21):8154-7. doi: 10.1021/ja203560q. Epub 2011 May 10. J Am Chem Soc. 2011. PMID: 21553917 Free PMC article.
A new family of stereoconvergent cross-couplings of unactivated secondary alkyl electrophiles has been developed, specifically, arylamine-directed alkyl-alkyl Suzuki reactions. This represents the first such investigation to be focused on the use of alkyl chlorides as subs …
A new family of stereoconvergent cross-couplings of unactivated secondary alkyl electrophiles has been developed, specifically, arylamine-di …
Old drug fluvoxamine, new hope for COVID-19.
Hashimoto Y, Suzuki T, Hashimoto K. Hashimoto Y, et al. Eur Arch Psychiatry Clin Neurosci. 2022 Feb;272(1):161-163. doi: 10.1007/s00406-021-01326-z. Epub 2021 Sep 2. Eur Arch Psychiatry Clin Neurosci. 2022. PMID: 34476589 Free PMC article. No abstract available.
Trifluoromethoxypyrazines: Preparation and Properties.
Sokolenko TM, Yagupolskii YL. Sokolenko TM, et al. Molecules. 2020 May 9;25(9):2226. doi: 10.3390/molecules25092226. Molecules. 2020. PMID: 32397388 Free PMC article.
As trifluoromethoxy-substituted pyrazines are still unknown, we have developed efficient and scalable methods for 2-chloro-5-trifluoromethoxypyrazine synthesis, showing the synthetic utility of this molecule for Buchwald-Hartwig amination and the Kumada-Corriu and Suzuk …
As trifluoromethoxy-substituted pyrazines are still unknown, we have developed efficient and scalable methods for 2-chloro-5-trifluoromethox …
5,311 results