172 related articles for article (PubMed ID: 30294503)
21. The mechanism of the Stevens and Sommelet-Hauser rearrangements. A theoretical study.
Ghigo G; Cagnina S; Maranzana A; Tonachini G
J Org Chem; 2010 Jun; 75(11):3608-17. PubMed ID: 20459136
[TBL] [Abstract][Full Text] [Related]
22. H12461. Fluorine as a Regiocontrol Element in the Ring Openings of Bicyclic Aziridiniums.
Lam YH; Houk KN; Cossy J; Prado DG; Cochi A
Helv Chim Acta; 2012 Nov; 95(11):2265-2277. PubMed ID: 23471532
[TBL] [Abstract][Full Text] [Related]
23. Theoretical insight into the regioselective ring-expansions of bicyclic aziridinium ions.
Boydas EB; Tanriver G; D'hooghe M; Ha HJ; Van Speybroeck V; Catak S
Org Biomol Chem; 2018 Jan; 16(5):796-806. PubMed ID: 29323389
[TBL] [Abstract][Full Text] [Related]
24. Opposite regiospecific ring opening of 2-(cyanomethyl)aziridines by hydrogen bromide and benzyl bromide: experimental study and theoretical rationalization.
Catak S; D'hooghe M; Verstraelen T; Hemelsoet K; Van Nieuwenhove A; Ha HJ; Waroquier M; De Kimpe N; Van Speybroeck V
J Org Chem; 2010 Jul; 75(13):4530-41. PubMed ID: 20507166
[TBL] [Abstract][Full Text] [Related]
25. The asymmetric synthesis of terminal aziridines by methylene transfer from sulfonium ylides to imines.
Kavanagh SA; Piccinini A; Connon SJ
Org Biomol Chem; 2013 Jun; 11(21):3535-40. PubMed ID: 23598787
[TBL] [Abstract][Full Text] [Related]
26. Photochemical ring expansion reactions: synthesis of tetrahydrofuran derivatives and mechanism studies.
Jana S; Yang Z; Pei C; Xu X; Koenigs RM
Chem Sci; 2019 Nov; 10(43):10129-10134. PubMed ID: 32015819
[TBL] [Abstract][Full Text] [Related]
27. Asymmetric Catalytic Ring-Expansion of 3-Methyleneazetidines with α-Diazo Pyrazoamides towards Proline-Derivatives.
Wang K; Yang L; Li Y; Li H; Liu Z; Ning L; Liu X; Feng X
Angew Chem Int Ed Engl; 2023 Aug; 62(32):e202307249. PubMed ID: 37316458
[TBL] [Abstract][Full Text] [Related]
28. Synthesis of 3-methoxyazetidines via an aziridine to azetidine rearrangement and theoretical rationalization of the reaction mechanism.
Stanković S; Catak S; D'hooghe M; Goossens H; Abbaspour Tehrani K; Bogaert P; Waroquier M; Van Speybroeck V; De Kimpe N
J Org Chem; 2011 Apr; 76(7):2157-67. PubMed ID: 21388111
[TBL] [Abstract][Full Text] [Related]
29. Synthesis of Aminomethylene-
Cheviet T; Peyrottes S
J Org Chem; 2021 Feb; 86(4):3107-3119. PubMed ID: 33476157
[TBL] [Abstract][Full Text] [Related]
30. Intramolecular pi-pi stacking interactions in 2-substituted N,N-dibenzylaziridinium ions and their regioselectivity in nucleophilic ring-opening reactions.
Catak S; D'hooghe M; De Kimpe N; Waroquier M; Van Speybroeck V
J Org Chem; 2010 Feb; 75(3):885-96. PubMed ID: 20039650
[TBL] [Abstract][Full Text] [Related]
31. Stereoselective Rearrangement of (Trifluoromethyl)prolinols to Enantioenriched 3-Substituted 2-(Trifluoromethyl)piperidines.
Rioton S; Orliac A; Antoun Z; Bidault R; Gomez Pardo D; Cossy J
Org Lett; 2015 Jun; 17(12):2916-9. PubMed ID: 26000643
[TBL] [Abstract][Full Text] [Related]
32. Three- and Four-Carbon Elongating Ring Expansion of Cyclic Acetals to Medium-Sized Dioxacycloalkenones. Use of the Intramolecular Formation of Oxonium Ylides.
Oku A; Murai N; Baird J
J Org Chem; 1997 Apr; 62(7):2123-2129. PubMed ID: 11671517
[TBL] [Abstract][Full Text] [Related]
33. 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]
34. Strain-Driven Dyotropic Rearrangement: A Unified Ring-Expansion Approach to α-Methylene-γ-butyrolactones.
Lei X; Li Y; Lai Y; Hu S; Qi C; Wang G; Tang Y
Angew Chem Int Ed Engl; 2021 Feb; 60(8):4221-4230. PubMed ID: 33155345
[TBL] [Abstract][Full Text] [Related]
35. Chemoselective allene aziridination via Ag(I) catalysis.
Rigoli JW; Weatherly CD; Vo BT; Neale S; Meis AR; Schomaker JM
Org Lett; 2013 Jan; 15(2):290-3. PubMed ID: 23265391
[TBL] [Abstract][Full Text] [Related]
36. Catalytic enantioselective intermolecular desymmetrization of azetidines.
Wang Z; Sheong FK; Sung HH; Williams ID; Lin Z; Sun J
J Am Chem Soc; 2015 May; 137(18):5895-8. PubMed ID: 25921194
[TBL] [Abstract][Full Text] [Related]
37. Computational investigations on the general reaction profile and diastereoselectivity in sulfur ylide promoted aziridination.
Janardanan D; Sunoj RB
Chemistry; 2007; 13(17):4805-15. PubMed ID: 17487905
[TBL] [Abstract][Full Text] [Related]
38. Modular functionalization of allenes to aminated stereotriads.
Adams CS; Boralsky LA; Guzei IA; Schomaker JM
J Am Chem Soc; 2012 Jul; 134(26):10807-10. PubMed ID: 22708990
[TBL] [Abstract][Full Text] [Related]
39. Competing Rearrangements of Ammonium Ylides: A Quantum Theoretical Study.
Heard GL; Yates BF
J Org Chem; 1996 Oct; 61(21):7276-7284. PubMed ID: 11667650
[TBL] [Abstract][Full Text] [Related]
40. Aziridinium ion ring formation from nitrogen mustards: mechanistic insights from ab initio dynamics.
Mann DJ
J Phys Chem A; 2010 Apr; 114(13):4486-93. PubMed ID: 20222705
[TBL] [Abstract][Full Text] [Related]
[Previous] [Next] [New Search]
