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.
149 related articles for article (PubMed ID: 29469220)
1. Mechanisms in Iodine Catalysis. Breugst M; von der Heiden D Chemistry; 2018 Jul; 24(37):9187-9199. PubMed ID: 29469220 [TBL] [Abstract][Full Text] [Related]
2. Reaction Mechanism of Iodine-Catalyzed Michael Additions. von der Heiden D; Bozkus S; Klussmann M; Breugst M J Org Chem; 2017 Apr; 82(8):4037-4043. PubMed ID: 28349682 [TBL] [Abstract][Full Text] [Related]
3. Electrophilic Activation of Iodonium Ylides by Halogen-Bond-Donor Catalysis for Cross-Enolate Coupling. Saito M; Kobayashi Y; Tsuzuki S; Takemoto Y Angew Chem Int Ed Engl; 2017 Jun; 56(26):7653-7657. PubMed ID: 28500729 [TBL] [Abstract][Full Text] [Related]
4. Iodoimidazolinium-Catalyzed Reduction of Quinoline by Hantzsch Ester: Halogen Bond or Brønsted Acid Catalysis. Ser CT; Yang H; Wong MW J Org Chem; 2019 Aug; 84(16):10338-10348. PubMed ID: 31283228 [TBL] [Abstract][Full Text] [Related]
5. Iodine-Catalyzed Claisen-Rearrangements of Allyl Aryl Ethers and Subsequent Iodocyclizations. Arndt T; Raina A; Breugst M Chem Asian J; 2023 Mar; 18(5):e202201279. PubMed ID: 36626351 [TBL] [Abstract][Full Text] [Related]
7. Chalcogen vs Halogen Bonding Catalysis in a Water-Bridge-Cocatalyzed Nitro-Michael Reaction. Tarannam N; Voelkel MHH; Huber SM; Kozuch S J Org Chem; 2022 Feb; 87(3):1661-1668. PubMed ID: 34181414 [TBL] [Abstract][Full Text] [Related]
8. The Pauli Repulsion-Lowering Concept in Catalysis. Hamlin TA; Bickelhaupt FM; Fernández I Acc Chem Res; 2021 Apr; 54(8):1972-1981. PubMed ID: 33759502 [TBL] [Abstract][Full Text] [Related]
9. Exploring the role of halogen bonding in iodonium ylides: insights into unexpected reactivity and reaction control. Montgomery CA; Murphy GK Beilstein J Org Chem; 2023; 19():1171-1190. PubMed ID: 37592937 [TBL] [Abstract][Full Text] [Related]
10. New developments in enantioselective Brønsted acid catalysis: chiral ion pair catalysis and beyond. Rueping M; Sugiono E Ernst Schering Found Symp Proc; 2007; (2):207-53. PubMed ID: 18642527 [TBL] [Abstract][Full Text] [Related]
14. Silylium ion-catalyzed challenging Diels-Alder reactions: the danger of hidden proton catalysis with strong Lewis acids. Schmidt RK; Müther K; Mück-Lichtenfeld C; Grimme S; Oestreich M J Am Chem Soc; 2012 Mar; 134(9):4421-8. PubMed ID: 22309027 [TBL] [Abstract][Full Text] [Related]
15. Iodine(I)-based and iodine(III)-based halogen bond catalysis on the Friedel-Crafts reaction: a theoretical study. Zhao C; Li Y; Li X; Zeng Y Phys Chem Chem Phys; 2023 Aug; 25(31):21100-21108. PubMed ID: 37527332 [TBL] [Abstract][Full Text] [Related]
16. Amino Acid-Derived Bifunctional Phosphines for Enantioselective Transformations. Wang T; Han X; Zhong F; Yao W; Lu Y Acc Chem Res; 2016 Jul; 49(7):1369-78. PubMed ID: 27310293 [TBL] [Abstract][Full Text] [Related]
17. Mukaiyama aldol reaction catalyzed by (benz)imidazolium-based halogen bond donors. Sutar RL; Erochok N; Huber SM Org Biomol Chem; 2021 Jan; 19(4):770-774. PubMed ID: 33432958 [TBL] [Abstract][Full Text] [Related]
18. Computational Insights into the Central Role of Nonbonding Interactions in Modern Covalent Organocatalysis. Walden DM; Ogba OM; Johnston RC; Cheong PH Acc Chem Res; 2016 Jun; 49(6):1279-91. PubMed ID: 27267964 [TBL] [Abstract][Full Text] [Related]
19. (1R)-(+)-camphor and acetone derived alpha'-hydroxy enones in asymmetric Diels-Alder reaction: catalytic activation by Lewis and Brønsted acids, substrate scope, applications in syntheses, and mechanistic studies. Bañuelos P; García JM; Gómez-Bengoa E; Herrero A; Odriozola JM; Oiarbide M; Palomo C; Razkin J J Org Chem; 2010 Mar; 75(5):1458-73. PubMed ID: 20121243 [TBL] [Abstract][Full Text] [Related]
20. Origin of asymmetric induction in bicyclic guanidine-catalyzed thio-Michael reaction: a bifunctional mode of Lewis acid-Brønsted acid activation. Cho B; Tan CH; Wong MW J Org Chem; 2012 Aug; 77(15):6553-62. PubMed ID: 22788383 [TBL] [Abstract][Full Text] [Related] [Next] [New Search]