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.
25. Electron transfer reduction of unactivated esters using SmI2-H2O. Szostak M; Spain M; Procter DJ Chem Commun (Camb); 2011 Oct; 47(37):10254-6. PubMed ID: 21858308 [TBL] [Abstract][Full Text] [Related]
26. SmI(2)-promoted radical addition of nitrones to alpha,beta-unsaturated amides and esters: synthesis of gamma-amino acids via a nitrogen equivalent to the ketyl radical. Riber D; Skrydstrup T Org Lett; 2003 Jan; 5(2):229-31. PubMed ID: 12529147 [TBL] [Abstract][Full Text] [Related]
27. Direct entry to peptidyl ketones via SmI2-mediated C-C bond formation with readily accessible N-peptidyl oxazolidinones. Mittag T; Christensen KL; Lindsay KB; Nielsen NC; Skrydstrup T J Org Chem; 2008 Feb; 73(3):1088-92. PubMed ID: 18163647 [TBL] [Abstract][Full Text] [Related]
28. Selective cleavage of 3,5-bis-(trifluoromethyl)benzylcarbamate by SmI2-Et3N-H2O. Ankner T; Stålsmeden AS; Hilmersson G Chem Commun (Camb); 2013 Aug; 49(61):6867-9. PubMed ID: 23792542 [TBL] [Abstract][Full Text] [Related]
29. SmI2-mediated coupling of nitrones and tert-butanesulfinyl imines with allenoates: synthesis of β-methylenyl-γ-lactams and tetramic acids. Xu CP; Huang PQ; Py S Org Lett; 2012 Apr; 14(8):2034-7. PubMed ID: 22489917 [TBL] [Abstract][Full Text] [Related]
30. Ketone-imide versus ketone-oxime reductive cross-coupling promoted by samarium diiodide: new mechanistic insight gained from a failed aminocyclopentitol synthesis. Chiara JL; García A; Cristóbal-Lumbroso G J Org Chem; 2005 May; 70(10):4142-51. PubMed ID: 15876107 [TBL] [Abstract][Full Text] [Related]
31. Estimating the limiting reducing power of SmI2/H2O/amine and YbI2/H2O/amine by efficient reduction of unsaturated hydrocarbons. Dahlén A; Nilsson A; Hilmersson G J Org Chem; 2006 Feb; 71(4):1576-80. PubMed ID: 16468808 [TBL] [Abstract][Full Text] [Related]
32. Selective reductions of cyclic 1,3-diesters by using SmI(2) and H(2)O. Collins KD; Oliveira JM; Guazzelli G; Sautier B; De Grazia S; Matsubara H; Helliwell M; Procter DJ Chemistry; 2010 Sep; 16(33):10240-9. PubMed ID: 20645340 [TBL] [Abstract][Full Text] [Related]
33. SmI2/water/amine mediates cleavage of allyl ether protected alcohols: application in carbohydrate synthesis and mechanistic considerations. Dahlén A; Sundgren A; Lahmann M; Oscarson S; Hilmersson G Org Lett; 2003 Oct; 5(22):4085-8. PubMed ID: 14572255 [TBL] [Abstract][Full Text] [Related]
34. Highly diastereoselective samarium diiodide induced cyclizations of new 3-substituted indole derivatives. Beemelmanns C; Reissig HU Org Biomol Chem; 2009 Nov; 7(21):4475-80. PubMed ID: 19830298 [TBL] [Abstract][Full Text] [Related]
35. Towards the core structure of Strychnos alkaloids using samarium diiodide-induced reactions of indole derivatives. Beemelmanns C; Gross S; Reissig HU Chemistry; 2013 Dec; 19(52):17801-8. PubMed ID: 24273006 [TBL] [Abstract][Full Text] [Related]
38. Mass spectrometric studies of cyclopentanol derivatives in the reductive coupling of alpha,beta-unsaturated ketones assisted by samarium diiodide. Le Lagadec R; Rubio L; Velasco L; Pérez-Flores J; Miranda R; Cabrera A Rapid Commun Mass Spectrom; 2003; 17(15):1699-702. PubMed ID: 12872273 [TBL] [Abstract][Full Text] [Related]
39. Determination of the effective redox potentials of SmI₂, SmBr₂, SmCl₂, and their complexes with water by reduction of aromatic hydrocarbons. Reduction of anthracene and stilbene by samarium(II) iodide-water complex. Szostak M; Spain M; Procter DJ J Org Chem; 2014 Mar; 79(6):2522-37. PubMed ID: 24517639 [TBL] [Abstract][Full Text] [Related]
40. Asymmetric conjugate reductions with samarium diiodide: asymmetric synthesis of (2S,3R)- and (2S,3S)-[2-2H,3-2H]-leucine-(S)-phenylalanine dipeptides and (2S,3R)-[2-(2)H,3-2H]-phenylalanine methyl ester. Davies SG; Rodriguez-Solla H; Tamayo JA; Cowley AR; Concellon C; Garner AC; Parkes AL; Smith AD Org Biomol Chem; 2005 Apr; 3(8):1435-47. PubMed ID: 15827639 [TBL] [Abstract][Full Text] [Related] [Previous] [Next] [New Search]