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Year Number of Results
1950 2
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1953 4
1954 6
1955 7
1956 11
1957 6
1958 5
1959 5
1960 2
1961 21
1962 33
1963 35
1964 33
1965 37
1966 35
1967 43
1968 53
1969 43
1970 49
1971 35
1972 46
1973 38
1974 61
1975 79
1976 47
1977 58
1978 78
1979 68
1980 111
1981 116
1982 119
1983 150
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1985 174
1986 192
1987 186
1988 192
1989 200
1990 190
1991 177
1992 218
1993 215
1994 202
1995 252
1996 254
1997 259
1998 318
1999 278
2000 288
2001 331
2002 297
2003 339
2004 388
2005 407
2006 463
2007 467
2008 460
2009 520
2010 525
2011 614
2012 628
2013 618
2014 659
2015 699
2016 666
2017 725
2018 647
2019 677
2020 706
2021 786
2022 740
2023 674
2024 236

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16,975 results

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Page 1
A Highly Stereospecific Claisen-Sakurai Approach to Densely Functionalized Cyclopentenols.
Stankevich KS, Cook MJ. Stankevich KS, et al. J Org Chem. 2022 Sep 16;87(18):12250-12256. doi: 10.1021/acs.joc.2c01397. Epub 2022 Sep 6. J Org Chem. 2022. PMID: 36067340
The formation of highly substituted cyclopentenols was developed using a Claisen-Sakurai reaction. Both elements of the reaction can be performed in a one-pot sequence that provides the corresponding cyclized products in high stereoselectivity. The stereochemical outcome i …
The formation of highly substituted cyclopentenols was developed using a Claisen-Sakurai reaction. Both elements of the reaction can …
A Stereoselective Reductive Hosomi-Sakurai Reaction.
Bauer A, Maulide N. Bauer A, et al. Org Lett. 2018 Mar 2;20(5):1461-1464. doi: 10.1021/acs.orglett.8b00276. Epub 2018 Feb 22. Org Lett. 2018. PMID: 29469578
A novel reductive variant of the classical Hosomi-Sakurai reaction is reported. This transformation hinges on a redox-neutral, stereoselective internal reduction event under mild conditions. ...
A novel reductive variant of the classical Hosomi-Sakurai reaction is reported. This transformation hinges on a redox-neutral, stereo …
Extraction of all propagation constants in a specified region from the transcendental equation of a dispersion relation using the Sakurai-Sugiura projection method.
Sato S, Shimada T, Hasegawa K. Sato S, et al. J Opt Soc Am A Opt Image Sci Vis. 2015 Jul 1;32(7):1216-21. doi: 10.1364/JOSAA.32.001216. J Opt Soc Am A Opt Image Sci Vis. 2015. PMID: 26367147
A transcendental equation occurs when we compute the dispersion relations of an electromagnetic waveguide, such as a planar multilayer waveguide. Without an initial guess, the Sakurai-Sugiura projection method (SSM) can obtain solutions to the transcendental equation in a …
A transcendental equation occurs when we compute the dispersion relations of an electromagnetic waveguide, such as a planar multilayer waveg …
A Sakurai-Prins-Ritter sequence for the three-component diastereoselective synthesis of 4-amino tetrahydropyrans.
Epstein OL, Rovis T. Epstein OL, et al. J Am Chem Soc. 2006 Dec 27;128(51):16480-1. doi: 10.1021/ja066794k. J Am Chem Soc. 2006. PMID: 17177379
A simple one-pot procedure for the Sakurai-Prins-Ritter sequence allows rapid assembly of 4-acylamino-2,6-substituted tetrahydropyrans in high yields and with excellent diastereoselectivity from readily available 4-acetoxy-1,3-dioxanes, allylsilanes, and nitriles. ...
A simple one-pot procedure for the Sakurai-Prins-Ritter sequence allows rapid assembly of 4-acylamino-2,6-substituted tetrahydropyran …
Tandem Sakurai-aldol addition reactions as a route to structurally complex carbocycles.
Stevens BD, Nelson SG. Stevens BD, et al. J Org Chem. 2005 May 27;70(11):4375-9. doi: 10.1021/jo050225y. J Org Chem. 2005. PMID: 15903314
Tandem intramolecular Sakurai-aldol reactions provide a concise and highly diastereoselective route to substituted cyclohexenone derivatives. The cyclization substrates are readily obtained using olefin isomerization-Claisen rearrangement (ICR) reactions to prepare the key …
Tandem intramolecular Sakurai-aldol reactions provide a concise and highly diastereoselective route to substituted cyclohexenone deri …
Sakurai responds.
Sakurai T. Sakurai T. Phys Rev Lett. 1986 Aug 11;57(6):781. doi: 10.1103/PhysRevLett.57.781. Phys Rev Lett. 1986. PMID: 10034158 No abstract available.
Functionalisation of isoindolinones via a calcium catalysed Hosomi-Sakurai allylation.
Basson AJ, McLaughlin MG. Basson AJ, et al. Chem Commun (Camb). 2019 Jul 11;55(57):8317-8320. doi: 10.1039/c9cc02450f. Chem Commun (Camb). 2019. PMID: 31257381
A rapid and functionally tolerant calcium catalysed Hosomi-Sakurai reaction has been realised. Employing 1 mol% calcium, allylated isoindolinones can be synthesised in high yields and the reaction is shown to be tolerant to a range of medicinally relevant functional groups …
A rapid and functionally tolerant calcium catalysed Hosomi-Sakurai reaction has been realised. Employing 1 mol% calcium, allylated is …
Trityl Cation-Catalyzed Hosomi-Sakurai Reaction of Allylsilane with beta,gamma-Unsaturated alpha-Ketoester to Form gamma,gamma-Disubstituted alpha-Ketoesters.
Gan Z, Cui D, Zhang H, Feng Y, Huang L, Gui Y, Gao L, Song Z. Gan Z, et al. Molecules. 2022 Jul 24;27(15):4730. doi: 10.3390/molecules27154730. Molecules. 2022. PMID: 35897907 Free PMC article.
(Ph(3)C)[BPh((F))(4)]-catalyzed Hosomi-Sakurai allylation of allylsilanes with beta,gamma-unsaturated alpha-ketoesters has been developed to give gamma,gamma-disubstituted alpha-ketoesters in high yields with excellent chemoselectivity. ...
(Ph(3)C)[BPh((F))(4)]-catalyzed Hosomi-Sakurai allylation of allylsilanes with beta,gamma-unsaturated alpha-ketoesters has been devel …
16,975 results
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