121 related articles for article (PubMed ID: 25081839)
1. Furanosyl oxocarbenium ion stability and stereoselectivity.
van Rijssel ER; van Delft P; Lodder G; Overkleeft HS; van der Marel GA; Filippov DV; Codée JD
Angew Chem Int Ed Engl; 2014 Sep; 53(39):10381-5. PubMed ID: 25081839
[TBL] [Abstract][Full Text] [Related]
2. Stereoselectivity in the Lewis acid mediated reduction of ketofuranoses.
van Rijssel ER; van Delft P; van Marle DV; Bijvoets SM; Lodder G; Overkleeft HS; van der Marel GA; Filippov DV; Codée JD
J Org Chem; 2015 May; 80(9):4553-65. PubMed ID: 25826382
[TBL] [Abstract][Full Text] [Related]
3. Furanosyl Oxocarbenium Ion Conformational Energy Landscape Maps as a Tool to Study the Glycosylation Stereoselectivity of 2-Azidofuranoses, 2-Fluorofuranoses and Methyl Furanosyl Uronates.
van der Vorm S; Hansen T; van Rijssel ER; Dekkers R; Madern JM; Overkleeft HS; Filippov DV; van der Marel GA; Codée JDC
Chemistry; 2019 May; 25(29):7149-7157. PubMed ID: 30882938
[TBL] [Abstract][Full Text] [Related]
4. Synthesis, Reactivity, and Stereoselectivity of 4-Thiofuranosides.
Madern JM; Hansen T; van Rijssel ER; Kistemaker HAV; van der Vorm S; Overkleeft HS; van der Marel GA; Filippov DV; Codée JDC
J Org Chem; 2019 Feb; 84(3):1218-1227. PubMed ID: 30605336
[TBL] [Abstract][Full Text] [Related]
5. Origin of Stereoselectivity in S
Remmerswaal WA; Hansen T; Hamlin TA; Codée JDC
Chemistry; 2023 Mar; 29(14):e202203490. PubMed ID: 36511875
[TBL] [Abstract][Full Text] [Related]
6. Stereoelectronic Model To Explain Highly Stereoselective Reactions of Seven-Membered-Ring Oxocarbenium-Ion Intermediates.
Beaver MG; Buscagan TM; Lavinda O; Woerpel KA
Angew Chem Int Ed Engl; 2016 Jan; 55(5):1816-9. PubMed ID: 26791884
[TBL] [Abstract][Full Text] [Related]
7. Scanning the potential energy surface of furanosyl oxocarbenium ions: models for reactive intermediates in glycosylation reactions.
Rhoad JS; Cagg BA; Carver PW
J Phys Chem A; 2010 Apr; 114(15):5180-6. PubMed ID: 20353189
[TBL] [Abstract][Full Text] [Related]
8. Nucleophilic additions of trimethylsilyl cyanide to cyclic oxocarbenium ions: evidence for the loss of stereoselectivity at the limits of diffusion control.
Shenoy SR; Smith DM; Woerpel KA
J Am Chem Soc; 2006 Jul; 128(26):8671-7. PubMed ID: 16802834
[TBL] [Abstract][Full Text] [Related]
9. Stereochemistry of nucleophilic substitution reactions depending upon substituent: evidence for electrostatic stabilization of pseudoaxial conformers of oxocarbenium ions by heteroatom substituents.
Ayala L; Lucero CG; Romero JA; Tabacco SA; Woerpel KA
J Am Chem Soc; 2003 Dec; 125(50):15521-8. PubMed ID: 14664599
[TBL] [Abstract][Full Text] [Related]
10. Reductive openings of benzylidene acetals revisited: a mechanistic scheme for regio- and stereoselectivity.
Johnsson R; Ohlin M; Ellervik U
J Org Chem; 2010 Dec; 75(23):8003-11. PubMed ID: 21033762
[TBL] [Abstract][Full Text] [Related]
11. Theoretical study on the factors controlling the stability of the borate complexes of ribose, arabinose, lyxose, and xylose.
Sponer JE; Sumpter BG; Leszczynski J; Sponer J; Fuentes-Cabrera M
Chemistry; 2008; 14(32):9990-8. PubMed ID: 18810746
[TBL] [Abstract][Full Text] [Related]
12. Glycosyl Oxocarbenium Ions: Structure, Conformation, Reactivity, and Interactions.
Franconetti A; Ardá A; Asensio JL; Blériot Y; Thibaudeau S; Jiménez-Barbero J
Acc Chem Res; 2021 Jun; 54(11):2552-2564. PubMed ID: 33930267
[TBL] [Abstract][Full Text] [Related]
13. Nucleophilic substitution reactions of sulfur-substituted cyclohexanone acetals: an analysis of the factors controlling stereoselectivity.
Billings SB; Woerpel KA
J Org Chem; 2006 Jul; 71(14):5171-8. PubMed ID: 16808503
[TBL] [Abstract][Full Text] [Related]
14. Nucleophilic substitution reactions of pyranose polytosylates.
McGeary RP; Rasoul Amini S; Tang VW; Toth I
J Org Chem; 2004 Apr; 69(8):2727-30. PubMed ID: 15074919
[TBL] [Abstract][Full Text] [Related]
15. Mechanism of a chemical glycosylation reaction.
Crich D
Acc Chem Res; 2010 Aug; 43(8):1144-53. PubMed ID: 20496888
[TBL] [Abstract][Full Text] [Related]
16. Stereoselectivity control by torsional steering in an intramolecular Diels-Alder reaction of vinyl oxocarbenium ions.
Iafe RG; Houk KN
Org Lett; 2006 Aug; 8(16):3469-72. PubMed ID: 16869637
[TBL] [Abstract][Full Text] [Related]
17. Using stereoelectronic effects to explain selective reactions of 4-substituted five-membered ring oxocarbenium ions.
Smith DM; Woerpel KA
Org Lett; 2004 Jun; 6(12):2063-6. PubMed ID: 15176819
[TBL] [Abstract][Full Text] [Related]
18. Stereoselective C-glycosylation reactions of ribose derivatives: electronic effects of five-membered ring oxocarbenium ions.
Larsen CH; Ridgway BH; Shaw JT; Smith DM; Woerpel KA
J Am Chem Soc; 2005 Aug; 127(31):10879-84. PubMed ID: 16076193
[TBL] [Abstract][Full Text] [Related]
19. Highly Stereoselective Glycosylation Reactions of Furanoside Derivatives via Rhenium (V) Catalysis.
Casali E; Othman ST; Dezaye AA; Chiodi D; Porta A; Zanoni G
J Org Chem; 2021 Jun; 86(11):7672-7686. PubMed ID: 34033490
[TBL] [Abstract][Full Text] [Related]
20. Substituent dependence of the diastereofacial selectivity in iodination and bromination of glycals and related cyclic enol ethers.
Boschi A; Chiappe C; De Rubertis A; Ruasse MF
J Org Chem; 2000 Dec; 65(25):8470-7. PubMed ID: 11112566
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
