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1846 3
1847 1
1849 1
1850 1
1851 8
1852 3
1854 1
1856 1
1857 1
1859 1
1866 2
1867 3
1870 2
1879 1
1899 1
1900 1
1905 2
1907 1
1908 1
1910 1
1912 1
1913 2
1914 1
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1918 1
1919 3
1920 6
1921 4
1922 3
1923 4
1924 2
1925 2
1926 8
1927 10
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1929 5
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1933 5
1934 5
1935 4
1936 4
1937 4
1938 8
1939 8
1940 8
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1942 7
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1967 2010
1968 2452
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1970 3080
1971 3742
1972 3931
1973 3548
1974 3592
1975 3723
1976 3425
1977 3249
1978 3077
1979 3306
1980 3629
1981 3714
1982 3913
1983 4069
1984 4620
1985 5117
1986 4992
1987 5181
1988 5429
1989 6305
1990 6452
1991 6635
1992 6451
1993 6576
1994 6680
1995 6532
1996 6675
1997 6513
1998 6656
1999 6671
2000 7126
2001 7345
2002 7377
2003 7758
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2005 8471
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The following term was not found in PubMed: ethyl-2-cyclopentenyl
Page 1
Second-Generation Total Synthesis of Prorocentin.
Yahata K, Zachmann RJ, Fürstner A. Yahata K, et al. Org Lett. 2023 Jul 7;25(26):4903-4907. doi: 10.1021/acs.orglett.3c01720. Epub 2023 Jun 26. Org Lett. 2023. PMID: 37358405 Free PMC article.
The revised entry starts from 2-deoxy-d-glucose; keys to success were a telescoped hemiacetal reduction/acetal cleavage and an exquisitely selective gold/Bronsted acid-cocatalyzed spiroacetalization....
The revised entry starts from 2-deoxy-d-glucose; keys to success were a telescoped hemiacetal reduction/acetal cleavage and an exquis …
Photoacid-catalyzed acetalization of carbonyls with alcohols.
Saway J, Pierre AF, Badillo JJ. Saway J, et al. Org Biomol Chem. 2022 Aug 10;20(31):6188-6192. doi: 10.1039/d2ob00435f. Org Biomol Chem. 2022. PMID: 35876112
In this report, we demonstrate that visible light photoactivation of 6-bromo-2-naphthol facilitates the photoacid-catalyzed acetalization of carbonyls with alcohols. We also demonstrate that 2-naphthol when coupled to a photosensitizer provides acetals from electron …
In this report, we demonstrate that visible light photoactivation of 6-bromo-2-naphthol facilitates the photoacid-catalyzed acetalization
Acetal containing polymers as pH-responsive nano-drug delivery systems.
Gannimani R, Walvekar P, Naidu VR, Aminabhavi TM, Govender T. Gannimani R, et al. J Control Release. 2020 Dec 10;328:736-761. doi: 10.1016/j.jconrel.2020.09.044. Epub 2020 Sep 25. J Control Release. 2020. PMID: 32980419 Review.
This review addresses the design and synthesis of various acetal-based polymers as pH-responsive nano-drug delivery systems in the form of micelles, polymersomes, nanoplexes and polymeric and solid lipid nanoparticles for biomedical applications. The review will identify p …
This review addresses the design and synthesis of various acetal-based polymers as pH-responsive nano-drug delivery systems in the fo …
Catalytic asymmetric transacetalization.
Corić I, Vellalath S, List B. Corić I, et al. J Am Chem Soc. 2010 Jun 30;132(25):8536-7. doi: 10.1021/ja102753d. J Am Chem Soc. 2010. PMID: 20527773
The chiral phosphoric acid TRIP was demonstrated to be an efficient and highly enantioselective catalyst for the activation of O,O-acetals. The reaction enables the asymmetric synthesis of acetals with the acetal carbon as the only stereogenic center....
The chiral phosphoric acid TRIP was demonstrated to be an efficient and highly enantioselective catalyst for the activation of O,O-acetal
Acetal-Based Functional Epoxide Monomers: Polymerizations and Applications.
Baek J, Kim M, Park Y, Kim BS. Baek J, et al. Macromol Biosci. 2021 Nov;21(11):e2100251. doi: 10.1002/mabi.202100251. Epub 2021 Aug 8. Macromol Biosci. 2021. PMID: 34369084 Review.
In this context, many functional epoxide monomers with proper protecting groups are developed, including the acetal group as a representative example. Since the early introduction of ethoxyethyl glycidyl ether, there is significant development of acetal-based monome …
In this context, many functional epoxide monomers with proper protecting groups are developed, including the acetal group as a repres …
TFA-Promoted Intermolecular Friedel-Crafts Alkylation of Arenes with 2,2,2-Trifluoroethylaryl Sulfoxides.
Deng Z, Qiu LY, Pan W, Qian B, Chen J, Zhang H, Chen QY, Cao W, Tang XJ. Deng Z, et al. Chem Asian J. 2022 Jul 15;17(14):e202200190. doi: 10.1002/asia.202200190. Epub 2022 Jun 10. Chem Asian J. 2022. PMID: 35644874
The classical Pummerer rearrangement of 2,2,2-trifluoroethylaryl sulfoxide with trifluoracetic anhydride (TFAA) affords the S,O-acetal efficiently. In the presence of trifluoracetic acid (TFA) as the co-solvent, the S,O-acetal can regenerate reactive thionium interm …
The classical Pummerer rearrangement of 2,2,2-trifluoroethylaryl sulfoxide with trifluoracetic anhydride (TFAA) affords the S,O-acetal
Degradable Glycopolyester-like Nanoparticles by Radical Ring-Opening Polymerization.
Pesenti T, Domingo-Lopez D, Gillon E, Ibrahim N, Messaoudi S, Imberty A, Nicolas J. Pesenti T, et al. Biomacromolecules. 2022 Sep 12;23(9):4015-4028. doi: 10.1021/acs.biomac.2c00851. Epub 2022 Aug 16. Biomacromolecules. 2022. PMID: 35971824
A small library of degradable polyester-like glycopolymers was successfully prepared by the combination of radical ring-opening copolymerization of 2-methylene-1,3-dioxepane as a cyclic ketene acetal (CKA) with vinyl ether (VE) derivatives and a Pd-catalyzed thioglycoconju …
A small library of degradable polyester-like glycopolymers was successfully prepared by the combination of radical ring-opening copolymeriza …
Oxylipin vanillyl acetals from Solanum lyratum.
Li SS, Liu QB, Zhang YY, Shi SC, Guo R, Yao GD, Lin B, Huang XX, Song SJ. Li SS, et al. Fitoterapia. 2020 Jun;143:104559. doi: 10.1016/j.fitote.2020.104559. Epub 2020 Mar 19. Fitoterapia. 2020. PMID: 32199958
Four undescribed oxylipin vanillyl acetals with four stereogenic carbons were isolated from the herbs of Solanum lyratum. ...The absolute configurations of the naturally occurring compounds are assigned as 7S, 9'S, 10'S, 11'R at the site of six-membered cyclic acetal
Four undescribed oxylipin vanillyl acetals with four stereogenic carbons were isolated from the herbs of Solanum lyratum. ...The abso …
Cyclic Acetals as Novel Long-Lasting Mosquito Repellents.
Iovinella I, Mandoli A, Luceri C, D'Ambrosio M, Caputo B, Cobre P, Dani FR. Iovinella I, et al. J Agric Food Chem. 2023 Feb 1;71(4):2152-2159. doi: 10.1021/acs.jafc.2c05537. Epub 2023 Jan 17. J Agric Food Chem. 2023. PMID: 36649540 Free PMC article.
Here, we tested against the mosquito Aedes albopictus several cyclic hydroxyacetals synthesized by acetalization of commercially available aliphatic carbonyl compounds (ranging from C3 to C15) with either glycerol, 1,1,1-trismethyloletane, or 1,1,1-trismethylolpropane and …
Here, we tested against the mosquito Aedes albopictus several cyclic hydroxyacetals synthesized by acetalization of commercially avai …
378,019 results
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