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1
Cross-coupling of mesylated phenol derivatives with potassium ammonio- and amidomethyltrifluoroborates.
Org Lett. 2011 Mar 4;13(5):1242-5. doi: 10.1021/ol200128y. Epub 2011 Feb 4.
2
Cross-coupling of mesylated phenol derivatives with potassium cyclopropyltrifluoroborate.
J Org Chem. 2011 Oct 7;76(19):8126-30. doi: 10.1021/jo2015246. Epub 2011 Sep 2.
3
Suzuki-Miyaura cross-coupling of potassium dioxolanylethyltrifluoroborate and aryl/heteroaryl chlorides.
Org Lett. 2013 Apr 5;15(7):1536-9. doi: 10.1021/ol400320q. Epub 2013 Mar 14.
4
Cross-coupling of mesylated phenol derivatives with potassium alkoxymethyltrifluoroborates.
Org Lett. 2011 Aug 5;13(15):3948-51. doi: 10.1021/ol201469r. Epub 2011 Jul 6.
5
Tetrabutylammonium 2-pyridyltriolborate salts for Suzuki-Miyaura cross-coupling reactions with aryl chlorides.
Org Lett. 2013 Sep 6;15(17):4308-11. doi: 10.1021/ol402268g. Epub 2013 Aug 16.
7
Potassium Boc-protected secondary aminomethyltrifluoroborates: synthesis and Suzuki-Miyaura cross-coupling reactions.
Org Lett. 2012 Sep 7;14(17):4458-61. doi: 10.1021/ol301955s. Epub 2012 Aug 29.
9
Oxidative condensations to form benzimidazole-substituted potassium organotrifluoroborates.
Org Lett. 2012 Aug 17;14(16):4242-5. doi: 10.1021/ol301956p. Epub 2012 Aug 8.

引用本文的文献

1
One-Pot Oxidative Amidation of Aldehydes via the Generation of Nitrile Imine Intermediates.
J Org Chem. 2024 Jun 7;89(11):7913-7926. doi: 10.1021/acs.joc.4c00575. Epub 2024 May 23.
2
Multicatalysis protocol enables direct and versatile enantioselective reductive transformations of secondary amides.
Sci Adv. 2022 Nov 25;8(47):eade3431. doi: 10.1126/sciadv.ade3431. Epub 2022 Nov 23.
3
Palladium-Catalyzed Cross-Couplings by C-O Bond Activation.
Catal Sci Technol. 2020 Sep 7;10(17):5702-5739. doi: 10.1039/d0cy01159b. Epub 2020 Jul 30.
4
Butenafine and analogues: An expeditious synthesis and cytotoxicity and antifungal activities.
J Adv Res. 2018 Jun 21;14:81-91. doi: 10.1016/j.jare.2018.06.004. eCollection 2018 Nov.
5
Facile synthesis of α-aminoboronic acids from amines and potassium acyltrifluoroborates (KATs) trifluoroborate-iminiums (TIMs).
Chem Sci. 2018 May 16;9(23):5191-5196. doi: 10.1039/c8sc01486h. eCollection 2018 Jun 21.
6
Suzuki-Miyaura cross-coupling of potassium trifluoro(N-methylheteroaryl)borates with aryl and heteroaryl halides.
J Org Chem. 2013 Jul 5;78(13):6648-56. doi: 10.1021/jo4009589. Epub 2013 Jun 25.
8
Microwave-enhanced cross-coupling reactions involving alkynyltrifluoroborates with aryl bromides.
Molecules. 2013 Jan 29;18(2):1755-61. doi: 10.3390/molecules18021755.
9
Suzuki-Miyaura cross-coupling of potassium alkoxyethyltrifluoroborates: access to aryl/heteroarylethyloxy motifs.
J Org Chem. 2012 Nov 16;77(22):10399-408. doi: 10.1021/jo3021665. Epub 2012 Nov 6.
10
Rapid and efficient access to secondary arylmethylamines.
Chemistry. 2012 Jul 27;18(31):9564-70. doi: 10.1002/chem.201200831. Epub 2012 Jul 5.

本文引用的文献

1
Reinvestigation of aminomethyltrifluoroborates and their application in Suzuki-Miyaura cross-coupling reactions.
J Org Chem. 2011 Apr 15;76(8):2762-9. doi: 10.1021/jo2001066. Epub 2011 Mar 15.
2
Nickel-catalyzed cross-couplings involving carbon-oxygen bonds.
Chem Rev. 2011 Mar 9;111(3):1346-416. doi: 10.1021/cr100259t. Epub 2010 Dec 6.
3
Stereospecific cross-coupling of secondary alkyl β-trifluoroboratoamides.
J Am Chem Soc. 2010 Dec 8;132(48):17108-10. doi: 10.1021/ja108949w. Epub 2010 Nov 15.
4
Synthesis of amidomethyltrifluoroborates and their use in cross-coupling reactions.
Org Lett. 2010 Nov 5;12(21):4876-9. doi: 10.1021/ol102039c.
7
Pharmacology and antitumor activity of ABC294640, a selective inhibitor of sphingosine kinase-2.
J Pharmacol Exp Ther. 2010 Apr;333(1):129-39. doi: 10.1124/jpet.109.163444. Epub 2010 Jan 8.
10
Suzuki-Miyaura cross-coupling reactions of primary alkyltrifluoroborates with aryl chlorides.
J Org Chem. 2009 May 15;74(10):3626-31. doi: 10.1021/jo900152n.

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