These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.
497 related articles for article (PubMed ID: 29039791)
1. Synthesis of Chiral TFA-Protected α-Amino Aryl-Ketone Derivatives with Friedel-Crafts Acylation of α-Amino Acid N-Hydroxysuccinimide Ester. Tachrim ZP; Oida K; Ikemoto H; Ohashi F; Kurokawa N; Hayashi K; Shikanai M; Sakihama Y; Hashidoko Y; Hashimoto M Molecules; 2017 Oct; 22(10):. PubMed ID: 29039791 [TBL] [Abstract][Full Text] [Related]
2. Facile approach to enantiomerically pure alpha-amino ketones by Friedel-Crafts aminoacylation and their conversion into peptidyl ketones. Di Gioia ML; Leggio A; Liguori A; Napoli A; Siciliano C; Sindona G J Org Chem; 2001 Oct; 66(21):7002-7. PubMed ID: 11597220 [TBL] [Abstract][Full Text] [Related]
3. Friedel-Crafts acylation with amides. Raja EK; DeSchepper DJ; Lill SO; Klumpp DA J Org Chem; 2012 Jul; 77(13):5788-93. PubMed ID: 22690740 [TBL] [Abstract][Full Text] [Related]
4. N-Tfa- and N-Fmoc-(alpha-aminoacyl)benzotriazoles as chiral C-acylating reagents under Friedel-Crafts reaction conditions. Katritzky AR; Jiang R; Suzuki K J Org Chem; 2005 Jun; 70(13):4993-5000. PubMed ID: 15960497 [TBL] [Abstract][Full Text] [Related]
5. Multicatalytic synthesis of alpha-pyrrolidinyl ketones via a tandem palladium(II)/indium(III)-catalyzed aminochlorocarbonylation/Friedel-Crafts acylation reaction. Cernak TA; Lambert TH J Am Chem Soc; 2009 Mar; 131(9):3124-5. PubMed ID: 19209934 [TBL] [Abstract][Full Text] [Related]
6. Utilization of acidic α-amino acids as acyl donors: an effective stereo-controllable synthesis of aryl-keto α-amino acids and their derivatives. Wang L; Murai Y; Yoshida T; Okamoto M; Tachrim ZP; Hashidoko Y; Hashimoto M Molecules; 2014 May; 19(5):6349-67. PubMed ID: 24840903 [TBL] [Abstract][Full Text] [Related]
7. In situ formation of N-trifluoroacetoxy succinimide (TFA-NHS): one-pot formation of succinimidyl esters, N-trifluoroacetyl amino acid succinimidyl esters, and N-maleoyl amino acid succinimidyl esters. Leonard NM; Brunckova J J Org Chem; 2011 Nov; 76(21):9169-74. PubMed ID: 21950593 [TBL] [Abstract][Full Text] [Related]
8. Progress in C-C and C-Heteroatom Bonds Construction Using Alcohols as Acyl Precursors. Zhao F; Tan B; Li Q; Tan Q; Huang H Molecules; 2022 Dec; 27(24):. PubMed ID: 36558110 [TBL] [Abstract][Full Text] [Related]
9. Autocatalytic one pot orchestration for the synthesis of α-arylated, α-amino esters. Roche SP; Samanta SS; Gosselin MM Chem Commun (Camb); 2014 Mar; 50(20):2632-4. PubMed ID: 24471165 [TBL] [Abstract][Full Text] [Related]
10. Biocatalytic Friedel-Crafts Acylation and Fries Reaction. Schmidt NG; Pavkov-Keller T; Richter N; Wiltschi B; Gruber K; Kroutil W Angew Chem Int Ed Engl; 2017 Jun; 56(26):7615-7619. PubMed ID: 28544673 [TBL] [Abstract][Full Text] [Related]
11. Friedel-Crafts Acylation of Aminocarboxylic Acids in Strong Brønsted Acid Promoted by Lewis Base P Wu H; Sumita A; Otani Y; Ohwada T J Org Chem; 2022 Nov; 87(22):15224-15249. PubMed ID: 36318089 [TBL] [Abstract][Full Text] [Related]
12. Novel syntheses of chiral beta- and gamma-amino acid derivatives utilizing N-protected (aminoacyl)benzotriazoles from aspartic and glutamic acids. Katritzky AR; Tao H; Jiang R; Suzuki K; Kirichenko K J Org Chem; 2007 Jan; 72(2):407-14. PubMed ID: 17221955 [TBL] [Abstract][Full Text] [Related]
13. Palladium-phosphinous acid-catalyzed cross-coupling of aryl and acyl halides with aryl-, alkyl-, and vinylzinc reagents. Xu H; Ekoue-Kovi K; Wolf C J Org Chem; 2008 Oct; 73(19):7638-50. PubMed ID: 18767805 [TBL] [Abstract][Full Text] [Related]
14. Esters as acylating reagent in a Friedel-Crafts reaction: indium tribromide catalyzed acylation of arenes using dimethylchlorosilane. Nishimoto Y; Babu SA; Yasuda M; Baba A J Org Chem; 2008 Dec; 73(23):9465-8. PubMed ID: 19007136 [TBL] [Abstract][Full Text] [Related]
15. Asymmetric α-arylation of amino acid derivatives by Clayden rearrangement of ester enolates via memory of chirality. Tomohara K; Yoshimura T; Hyakutake R; Yang P; Kawabata T J Am Chem Soc; 2013 Sep; 135(36):13294-7. PubMed ID: 23957387 [TBL] [Abstract][Full Text] [Related]