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.
188 related articles for article (PubMed ID: 35689000)
1. N-Aminopyridinium reagents as traceless activating groups in the synthesis of N-Aryl aziridines. Tan H; Samanta S; Maity A; Roychowdhury P; Powers DC Nat Commun; 2022 Jun; 13(1):3341. PubMed ID: 35689000 [TBL] [Abstract][Full Text] [Related]
2. Rh Deng T; Mazumdar W; Yoshinaga Y; Patel PB; Malo D; Malo T; Wink DJ; Driver TG J Am Chem Soc; 2021 Nov; 143(45):19149-19159. PubMed ID: 34748699 [TBL] [Abstract][Full Text] [Related]
3. Palladium-Catalyzed Regioselective and Stereospecific Ring-Opening Cross-Coupling of Aziridines: Experimental and Computational Studies. Takeda Y; Sameera WMC; Minakata S Acc Chem Res; 2020 Aug; 53(8):1686-1702. PubMed ID: 32786337 [TBL] [Abstract][Full Text] [Related]
4. Synthesis of β-Phenethylamines via Ni/Photoredox Cross-Electrophile Coupling of Aliphatic Aziridines and Aryl Iodides. Steiman TJ; Liu J; Mengiste A; Doyle AG J Am Chem Soc; 2020 Apr; 142(16):7598-7605. PubMed ID: 32250602 [TBL] [Abstract][Full Text] [Related]
5. Metalated aziridines for cross-coupling with aryl and alkenyl halides via palladium catalysis. Nelson JM; Vedejs E Org Lett; 2010 Nov; 12(22):5085-7. PubMed ID: 20945857 [TBL] [Abstract][Full Text] [Related]
6. Application of chiral N-tert-butylsulfinyl vinyl aziridines in Rh(I) catalyzed 1,4-addition of aryl boronic acids to cyclic enones. Chen Q; Chen C; Guo F; Xia W Chem Commun (Camb); 2013 Jul; 49(57):6433-5. PubMed ID: 23756467 [TBL] [Abstract][Full Text] [Related]
7. β-Phenethylamine Synthesis: N-Pyridinium Aziridines as Latent Dual Electrophiles. Samanta S; Biswas P; O'Bannon BC; Powers DC Angew Chem Int Ed Engl; 2024 Jul; 63(31):e202406335. PubMed ID: 38699820 [TBL] [Abstract][Full Text] [Related]
8. Role of Electron-Deficient Olefin Ligands in a Ni-Catalyzed Aziridine Cross-Coupling To Generate Quaternary Carbons. Estrada JG; Williams WL; Ting SI; Doyle AG J Am Chem Soc; 2020 May; 142(19):8928-8937. PubMed ID: 32348673 [TBL] [Abstract][Full Text] [Related]
17. Copper Catalyzed Regioselective and Stereospecific Aziridine Opening with Pyridyl Grignard Nucleophiles. Lee J; Ju X; Lee M; Jiang Q; Jang H; Kim WS; Wu L; Williams S; Wang XJ; Zeng X; Payne J; Han ZS Org Lett; 2022 Apr; 24(14):2655-2659. PubMed ID: 35377668 [TBL] [Abstract][Full Text] [Related]
18. Nucleophilic ring opening reactions of aziridines. Akhtar R; Naqvi SAR; Zahoor AF; Saleem S Mol Divers; 2018 May; 22(2):447-501. PubMed ID: 29728870 [TBL] [Abstract][Full Text] [Related]
19. Aziridines from intramolecular alkene aziridination of sulfamates: reactivity toward carbon nucleophiles. application to the synthesis of spisulosine and its fluoro analogue. Malik G; Estéoule A; Retailleau P; Dauban P J Org Chem; 2011 Sep; 76(18):7438-48. PubMed ID: 21812488 [TBL] [Abstract][Full Text] [Related]
20. β-amino esters from the reductive ring opening of aziridine-2-carboxylates. Zhao W; Lu Z; Wulff WD J Org Chem; 2014 Nov; 79(21):10068-80. PubMed ID: 25329528 [TBL] [Abstract][Full Text] [Related] [Next] [New Search]