203 related articles for article (PubMed ID: 23117425)
1. The Kabachnik-Fields reaction: mechanism and synthetic use.
Keglevich G; Bálint E
Molecules; 2012 Nov; 17(11):12821-35. PubMed ID: 23117425
[TBL] [Abstract][Full Text] [Related]
2. Study on the Microwave-Assisted Batch and Continuous Flow Synthesis of
Tajti Á; Tóth N; Rávai B; Csontos I; Szabó PT; Bálint E
Molecules; 2020 Jul; 25(14):. PubMed ID: 32708227
[TBL] [Abstract][Full Text] [Related]
3. Microwave-Assisted Kabachnik⁻Fields Reaction with Amino Alcohols as the Amine Component.
Tajti Á; Szatmári E; Perdih F; Keglevich G; Bálint E
Molecules; 2019 Apr; 24(8):. PubMed ID: 31027303
[TBL] [Abstract][Full Text] [Related]
4. Synthesis of α-Aminophosphonates and Related Derivatives; the Last Decade of the Kabachnik-Fields Reaction.
Varga PR; Keglevich G
Molecules; 2021 Apr; 26(9):. PubMed ID: 33923090
[TBL] [Abstract][Full Text] [Related]
5. An extremely efficient three-component reaction of aldehydes/ketones, amines, and phosphites (Kabachnik-Fields reaction) for the synthesis of alpha-aminophosphonates catalyzed by magnesium perchlorate.
Bhagat S; Chakraborti AK
J Org Chem; 2007 Feb; 72(4):1263-70. PubMed ID: 17253748
[TBL] [Abstract][Full Text] [Related]
6. Efficient one-pot, three-component procedure to prepare new α-aminophosphonate and phosphonic acid acyclic nucleosides.
Baddi L; Ouzebla D; El Mansouri AE; Smietana M; Vasseur JJ; Lazrek HB
Nucleosides Nucleotides Nucleic Acids; 2021; 40(1):43-67. PubMed ID: 33030107
[TBL] [Abstract][Full Text] [Related]
7.
Keglevich G; Varga PR; Dinnyési E; Szalai Z; Bősze S; Rita OS; Drahos L; Karaghiosoff K
Org Biomol Chem; 2024 May; 22(19):3940-3950. PubMed ID: 38682553
[TBL] [Abstract][Full Text] [Related]
8. Microwaves as "Co-Catalysts" or as Substitute for Catalysts in Organophosphorus Chemistry.
Keglevich G
Molecules; 2021 Feb; 26(4):. PubMed ID: 33672361
[TBL] [Abstract][Full Text] [Related]
9. Heterogeneous catalyst SiO
Basha SKT; Kalla RMN; Varalakshmi M; Sudhamani H; Appa RM; Chul Hong S; Raju CN
Mol Divers; 2022 Oct; 26(5):2703-2715. PubMed ID: 35034246
[TBL] [Abstract][Full Text] [Related]
10. New
Varga PR; Karaghiosoff K; Sári ÉV; Simon A; Hegedűs L; Drahos L; Keglevich G
Org Biomol Chem; 2023 Feb; 21(8):1709-1718. PubMed ID: 36723166
[TBL] [Abstract][Full Text] [Related]
11. The Last Decade of Optically Active α-Aminophosphonates.
Varga PR; Keglevich G
Molecules; 2023 Aug; 28(16):. PubMed ID: 37630402
[TBL] [Abstract][Full Text] [Related]
12. Enantioselective three-component Kabachnik-Fields reaction catalyzed by chiral scandium(III)-N,N'-dioxide complexes.
Zhou X; Shang D; Zhang Q; Lin L; Liu X; Feng X
Org Lett; 2009 Mar; 11(6):1401-4. PubMed ID: 19226133
[TBL] [Abstract][Full Text] [Related]
13. Microwave-assisted synthesis of
Bálint E; Tripolszky A; Hegedűs L; Keglevich G
Beilstein J Org Chem; 2019; 15():469-473. PubMed ID: 30873230
[TBL] [Abstract][Full Text] [Related]
14. Catalyst-free synthesis of α
Molleti N; Yong Kang J
Org Biomol Chem; 2016 Sep; 14(38):8952-8956. PubMed ID: 27722586
[TBL] [Abstract][Full Text] [Related]
15. Continuous Flow Esterification of a
Kiss NZ; Henyecz R; Keglevich G
Molecules; 2020 Feb; 25(3):. PubMed ID: 32046016
[TBL] [Abstract][Full Text] [Related]
16. Redox-neutral α-C-H bond functionalization of secondary amines with concurrent C-P bond formation/N-alkylation.
Das D; Seidel D
Org Lett; 2013 Sep; 15(17):4358-61. PubMed ID: 23957378
[TBL] [Abstract][Full Text] [Related]
17. A highly efficient bismuth salts-catalyzed route for the synthesis of α-aminophosphonates.
Banik A; Batta S; Bandyopadhyay D; Banik BK
Molecules; 2010 Nov; 15(11):8205-13. PubMed ID: 21076387
[TBL] [Abstract][Full Text] [Related]
18. Reaction of 2H-azirine phosphine oxide and -phosphonates with nucleophiles. Stereoselective Synthesis of functionalized aziridines and alpha- and beta-aminophosphorus derivatives.
Palacios F; de Retana AM; Alonso JM
J Org Chem; 2005 Oct; 70(22):8895-901. PubMed ID: 16238324
[TBL] [Abstract][Full Text] [Related]
19. Phospha-Michael addition reaction of maleimides employing N-heterocyclic phosphine-thiourea as a phosphonylation reagent: synthesis of 1-aryl-2,5-dioxopyrrolidine-3-yl-phosphonate derivatives.
Molleti N; Bjornberg C; Kang JY
Org Biomol Chem; 2016 Dec; 14(45):10695-10704. PubMed ID: 27805222
[TBL] [Abstract][Full Text] [Related]
20. One pot synthesis of alpha-aminophosphonates containing bromo and 3,4,5-trimethoxybenzyl groups under solvent-free conditions.
Li C; Song B; Yan K; Xu G; Hu D; Yang S; Jin L; Xue W; Lu P
Molecules; 2007 Feb; 12(2):163-72. PubMed ID: 17846566
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
