Year |
Citation |
Score |
2015 |
Janjetovic M, Träff AM, Hilmersson G. Mild and selective activation and substitution of strong aliphatic C-F bonds. Chemistry (Weinheim An Der Bergstrasse, Germany). 21: 3772-7. PMID 25601723 DOI: 10.1002/chem.201406097 |
0.3 |
|
2013 |
Ankner T, Stålsmeden AS, Hilmersson G. Selective cleavage of 3,5-bis-(trifluoromethyl)benzylcarbamate by SmI2-Et3N-H2O. Chemical Communications (Cambridge, England). 49: 6867-9. PMID 23792542 DOI: 10.1039/C3Cc41642A |
0.754 |
|
2013 |
Janjetovic M, Träff AM, Ankner T, Wettergren J, Hilmersson G. Solvent dependent reductive defluorination of aliphatic C-F bonds employing Sm(HMDS)2. Chemical Communications (Cambridge, England). 49: 1826-8. PMID 23358653 DOI: 10.1039/C3Cc37828D |
0.772 |
|
2012 |
Rönnholm P, Gräfenstein J, Norrby PO, Hilmersson G, Lill SO. A computational study of the enantioselective addition of n-BuLi to benzaldehyde in the presence of a chiral lithium N,P amide. Organic & Biomolecular Chemistry. 10: 2807-14. PMID 22378179 DOI: 10.1039/C2Ob06910E |
0.668 |
|
2012 |
Rönnholm P, Lill SON, Gräfenstein J, Norrby PO, Pettersson M, Hilmersson G. Aggregation and solvation of chiral N, P-amide ligands in coordinating solvents: A computational and NMR spectroscopic study Chempluschem. 77: 799-806. DOI: 10.1002/Cplu.201200033 |
0.626 |
|
2011 |
Rönnholm P, Hilmersson G. NMR studies of chiral lithium amides with phosphine chelating groups reveal strong Li-P-interactions in ethereal solvents Arkivoc. 2011: 200-210. DOI: 10.3998/Ark.5550190.0012.517 |
0.513 |
|
2010 |
Carbone G, O'Brien P, Hilmersson G. Asymmetric deprotonation using s-BuLi or i-PrLi and chiral diamines in THF: the diamine matters. Journal of the American Chemical Society. 132: 15445-50. PMID 20936816 DOI: 10.1021/Ja107672H |
0.502 |
|
2010 |
Wettergren J, Ankner T, Hilmersson G. Selective α-defluorination of polyfluorinated esters and amides using SmI2/Et3N/H2O. Chemical Communications (Cambridge, England). 46: 7596-7. PMID 20838692 DOI: 10.1039/C0Cc02009E |
0.777 |
|
2010 |
Ankner T, Fridén-Saxin M, Pemberton N, Seifert T, Grøtli M, Luthman K, Hilmersson G. KHMDS enhanced SmI(2)-mediated reformatsky type alpha-cyanation. Organic Letters. 12: 2210-3. PMID 20429501 DOI: 10.1021/Ol100424Y |
0.756 |
|
2010 |
Lennartson A, Sundberg J, Wiklund T, Hilmersson G, Håkansson M. Spontaneous resolution and carbonation of chiral Benzylithium complexes European Journal of Inorganic Chemistry. 3029-3039. DOI: 10.1002/Ejic.200901172 |
0.443 |
|
2009 |
Ankner T, Hilmersson G. Instantaneous deprotection of tosylamides and esters with SmI(2)/amine/water. Organic Letters. 11: 503-6. PMID 19123840 DOI: 10.1021/Ol802243D |
0.768 |
|
2009 |
Ankner T, Hilmersson G. SmI2/H2O/amine promoted reductive cleavage of benzyl-heteroatom bonds: optimization and mechanism Tetrahedron. 65: 10856-10862. DOI: 10.1016/J.Tet.2009.10.086 |
0.786 |
|
2009 |
Hilmersson G, Granander J. Structure and Dynamics of Chiral Lithium Amides Patai's Chemistry of Functional Groups. 381-409. DOI: 10.1002/9780470682531.Pat0342 |
0.752 |
|
2007 |
Rönnholm P, Södergren M, Hilmersson G. Improved and efficient synthesis of chiral N,P-ligands via cyclic sulfamidates for asymmetric addition of butyllithium to benzaldehyde. Organic Letters. 9: 3781-3. PMID 17696545 DOI: 10.1021/Ol701504C |
0.485 |
|
2007 |
Ankner T, Hilmersson G. Instantaneous SmI2/H2O/amine mediated reduction of nitroalkanes and α,β-unsaturated nitroalkenes Tetrahedron Letters. 48: 5707-5710. DOI: 10.1016/J.Tetlet.2007.05.105 |
0.746 |
|
2006 |
Granander J, Sott R, Hilmersson G. Correlation between the 6Li,15N coupling constant and the coordination number at lithium. Chemistry (Weinheim An Der Bergstrasse, Germany). 12: 4191-7. PMID 16526078 DOI: 10.1002/Chem.200501371 |
0.783 |
|
2006 |
Dahlén A, Nilsson A, Hilmersson G. Estimating the limiting reducing power of SmI2/H2O/amine and YbI2/H2O/amine by efficient reduction of unsaturated hydrocarbons. The Journal of Organic Chemistry. 71: 1576-80. PMID 16468808 DOI: 10.1021/Jo052268K |
0.618 |
|
2006 |
Sott R, Håkansson M, Hilmersson G. Studies of complexes between phenyllithium and (-)-sparteine in ether solutions Organometallics. 25: 6047-6053. DOI: 10.1021/Om050872F |
0.781 |
|
2006 |
Granander J, Eriksson J, Hilmersson G. Highly enantioselective 1,2-additions of various organolithium reagents to aldehydes Tetrahedron Asymmetry. 17: 2021-2027. DOI: 10.1016/j.tetasy.2006.07.009 |
0.38 |
|
2006 |
Granander J, Eriksson J, Hilmersson G. Highly enantioselective 1,2-additions of various organolithium reagents to aldehydes Tetrahedron Asymmetry. 17: 2021-2027. DOI: 10.1016/J.Tetasy.2006.07.009 |
0.831 |
|
2005 |
Dahlén A, Hilmersson G. Mechanistic study of the SmI2/H2O/amine-mediated reduction of alkyl halides: amine base strength (pKBH+) dependent rate. Journal of the American Chemical Society. 127: 8340-7. PMID 15941267 DOI: 10.1021/Ja043323U |
0.657 |
|
2005 |
Sott R, Granander J, Williamson C, Hilmersson G. Kinetic and NMR spectroscopic studies of chiral mixed sodium/lithium amides used for the deprotonation of cyclohexene oxide. Chemistry (Weinheim An Der Bergstrasse, Germany). 11: 4785-92. PMID 15929140 DOI: 10.1002/Chem.200500121 |
0.799 |
|
2005 |
Dahlén A, Prasad E, Flowers RA, Hilmersson G. Exploring SmBr2-, SmI2-, and YbI2-mediated reactions assisted by microwave irradiation. Chemistry (Weinheim An Der Bergstrasse, Germany). 11: 3279-84. PMID 15786498 DOI: 10.1002/Chem.200401320 |
0.693 |
|
2004 |
Sott R, Granander J, Hilmersson G. Mixed complexes formed by lithioacetonitrile and chiral lithium amides: observation of (6)li,(15)N and (6)Li,(13)C couplings due to both C-Li and N-Li contacts. Journal of the American Chemical Society. 126: 6798-805. PMID 15161308 DOI: 10.1021/Ja0388461 |
0.793 |
|
2004 |
Sott R, Granander J, Dinér P, Hilmersson G. Solution structures of chiral lithium amides with internal sulfide coordination: Sulfide versus ether coordination in chiral lithium amides Tetrahedron Asymmetry. 15: 267-274. DOI: 10.1016/j.tetasy.2003.11.009 |
0.358 |
|
2004 |
Sott R, Granander J, Dinér P, Hilmersson G. Solution structures of chiral lithium amides with internal sulfide coordination: Sulfide versus ether coordination in chiral lithium amides Tetrahedron Asymmetry. 15: 267-274. DOI: 10.1016/J.Tetasy.2003.11.009 |
0.816 |
|
2004 |
Dahlén A, Hilmersson G. Samarium(II) iodide mediated reductions - Influence of various additives European Journal of Inorganic Chemistry. 3393-3403. DOI: 10.1002/Ejic.200400442 |
0.665 |
|
2004 |
Dahlén A, Hilmersson G. Microwave-assisted generation of lanthanide(II) halides in THF and simple quantitative determination European Journal of Inorganic Chemistry. 3020-3024. DOI: 10.1002/Ejic.200400309 |
0.662 |
|
2003 |
Dahlén A, Sundgren A, Lahmann M, Oscarson S, Hilmersson G. SmI2/water/amine mediates cleavage of allyl ether protected alcohols: application in carbohydrate synthesis and mechanistic considerations. Organic Letters. 5: 4085-8. PMID 14572255 DOI: 10.1021/Ol0354831 |
0.772 |
|
2003 |
Dahlén A, Petersson A, Hilmersson G. Diastereoselective intramolecular SmI2-H2O-amine mediated couplings. Organic & Biomolecular Chemistry. 1: 2423-6. PMID 12956056 DOI: 10.1039/B305428D |
0.761 |
|
2003 |
Dahlén A, Hilmersson G, Knettle BW, Flowers RA. Rapid SmI2-mediated reductions of alkyl halides and electrochemical properties of SmI2/H2O/amine. The Journal of Organic Chemistry. 68: 4870-5. PMID 12790593 DOI: 10.1021/Jo034173T |
0.797 |
|
2003 |
Dahlén A, Hilmersson G. Instantaneous SmI2/H2O/amine-mediated reductions in THF. Chemistry (Weinheim An Der Bergstrasse, Germany). 9: 1123-8. PMID 12596148 DOI: 10.1002/Chem.200390129 |
0.766 |
|
2003 |
Granander J, Sott R, Hilmersson G. Chiral lithium amido sulfide ligands for asymmetric addition reactions of alkyllithium reagents to aldehydes Tetrahedron Asymmetry. 14: 439-447. DOI: 10.1016/S0957-4166(02)00864-9 |
0.797 |
|
2003 |
Granander J, Sott R, Hilmersson G. Chiral lithium amido sulfide ligands for asymmetric addition reactions of alkyllithium reagents to aldehydes Tetrahedron Asymmetry. 14: 439-447. DOI: 10.1016/S0957-4166(02)00864-9 |
0.388 |
|
2003 |
Dahlén A, Hilmersson G. Selective reduction of carbon-carbon double and triple bonds in conjugated olefins mediated by SmI2/H2O/amine in THF Tetrahedron Letters. 44: 2661-2664. DOI: 10.1016/S0040-4039(03)00369-1 |
0.773 |
|
2003 |
Vestergren M, Eriksson J, Hilmersson G, Håkansson M. Giving phenyllithium a right-handed double-helical twist. Syntheses and crystal structures of enantiopure alkyl-, aryl-, and amidolithium aggregates Journal of Organometallic Chemistry. 682: 172-179. DOI: 10.1016/S0022-328X(03)00779-4 |
0.383 |
|
2003 |
Kim M, Knettle BW, Dahlén A, Hilmersson G, Flowers RA. Reduction and reductive coupling of imines by Sm(II)-based reagents Tetrahedron. 59: 10397-10402. DOI: 10.1016/J.Tet.2003.06.004 |
0.655 |
|
2002 |
Sott R, Granander J, Hilmersson G. Solvent-dependent mixed complex formation-NMR studies and asymmetric addition reactions of lithioacetonitrile to benzaldehyde mediated by chiral lithium amides. Chemistry (Weinheim An Der Bergstrasse, Germany). 8: 2081-7. PMID 11981893 DOI: 10.1002/1521-3765(20020503)8:9<2081::Aid-Chem2081>3.0.Co;2-Q |
0.819 |
|
2002 |
Johansson A, Hilmersson G, Davidsson O. Chelate ring size controls the formation of mixed complexes involving butyllithium and sodium amides Organometallics. 21: 2283-2292. DOI: 10.1021/Om0109410 |
0.465 |
|
2002 |
Dahlén A, Hilmersson G. Instantaneous SmI2-H2O-mediated reduction of dialkyl ketones induced by amines in THF Tetrahedron Letters. 43: 7197-7200. DOI: 10.1016/S0040-4039(02)01673-8 |
0.756 |
|
2002 |
Granander J, Sott R, Hilmersson G. Asymmetric addition of n-butyllithium to aldehydes: New insights into the reactivity and enantioselectivity of the chiral amino ether accelerated reaction Tetrahedron. 58: 4717-4725. DOI: 10.1016/S0040-4020(02)00378-2 |
0.823 |
|
2002 |
Granander J, Sott R, Hilmersson G. Asymmetric addition of n-butyllithium to aldehydes: New insights into the reactivity and enantioselectivity of the chiral amino ether accelerated reaction Tetrahedron. 58: 4717-4725. DOI: 10.1016/S0040-4020(02)00378-2 |
0.803 |
|
2002 |
Arvidsson PI, Hilmersson G, Davidsson O?. On the mechanism of internal ortho-lithiation in a mixed complex between BuLi and a chiral lithium amide Helvetica Chimica Acta. 85: 3814-3822. DOI: 10.1002/1522-2675(200211)85:11<3814::Aid-Hlca3814>3.0.Co;2-O |
0.479 |
|
2002 |
Arvidsson PI, Hilmersson G, Davidsson O?. On the mechanism of internal ortho-lithiation in a mixed complex between BuLi and a chiral lithium amide Helvetica Chimica Acta. 85: 3814-3822. DOI: 10.1002/1522-2675(200211)85:11<3814::AID-HLCA3814>3.0.CO;2-O |
0.342 |
|
2002 |
Sott R, Granander J, Hilmersson G. Solvent-dependent mixed complex formation - NMR studies and asymmetric addition reactions of lithioacetonitrile to benzaldehyde mediated by chiral lithium amides Chemistry - a European Journal. 8: 2081-2087. DOI: 10.1002/1521-3765(20020503)8:9<2081::AID-CHEM2081>3.0.CO;2-Q |
0.81 |
|
2002 |
Sott R, Granander J, Hilmersson G. Solvent-dependent mixed complex formation - NMR studies and asymmetric addition reactions of lithioacetonitrile to benzaldehyde mediated by chiral lithium amides Chemistry - a European Journal. 8: 2081-2087. DOI: 10.1002/1521-3765(20020503)8:9<2081::AID-CHEM2081>3.0.CO;2-Q |
0.446 |
|
2001 |
Hilmersson G, Malmros B. Mixed dimer and mixed trimer complexes of nBuLi and a chiral lithium amide. Chemistry (Weinheim An Der Bergstrasse, Germany). 7: 337-41. PMID 11271518 DOI: 10.1002/1521-3765(20010119)7:2<337::Aid-Chem337>3.0.Co;2-I |
0.454 |
|
2001 |
Dahlén A, Hilmersson G. Chelating alcohols accelerate the samarium diiodide mediated reduction of 3-heptanone Tetrahedron Letters. 42: 5565-5569. DOI: 10.1016/S0040-4039(01)00958-3 |
0.75 |
|
2000 |
Hilmersson G. An NMR and computational study of a lithium amide and ethereal ligand exchange Chemistry (Weinheim An Der Bergstrasse, Germany). 6: 3069-75. PMID 10993268 DOI: 10.1002/1521-3765(20000818)6:16<3069::Aid-Chem3069>3.0.Co;2-5 |
0.385 |
|
1999 |
Håkansson M, Vestergren M, Gustafsson B, Hilmersson G. Isolation and Spontaneous Resolution of Eight-Coordinate Stereoisomers. Angewandte Chemie (International Ed. in English). 38: 2199-2201. PMID 10425480 DOI: 10.1002/(Sici)1521-3773(19990802)38:15<2199::Aid-Anie2199>3.0.Co;2-S |
0.379 |
|
1999 |
Santamaría J, Martín T, Hilmersson G, Craig SL, Rebek J. Guest exchange in an encapsulation complex: a supramolecular substitution reaction. Proceedings of the National Academy of Sciences of the United States of America. 96: 8344-7. PMID 10411877 DOI: 10.1073/Pnas.96.15.8344 |
0.582 |
|
1999 |
Karlsson A, Hilmersson G, Davidsson O, Löwendahl M, Ahlberg P. Solvent catalysis, mechanisms of degenerate metallation and solvation of ferrocenophanylpotassium and ferrocenophanylsodium studied by UV and NMR spectroscopy Acta Chemica Scandinavica. 53: 693-698. DOI: 10.3891/Acta.Chem.Scand.53-0693 |
0.534 |
|
1999 |
Arvidsson PI, Hilmersson G, Ahlberg P. Stereoselective diamine chelates of a chiral lithium amide dimer: New insights into the coordination chemistry of chiral lithium amides Journal of the American Chemical Society. 121: 1883-1887. DOI: 10.1021/Ja9827550 |
0.661 |
|
1999 |
Arvidsson PI, Hilmersson G, Ahlberg P. Stereoselective diamine chelates of a chiral lithium amide dimer: New insights into the coordination chemistry of chiral lithium amides Journal of the American Chemical Society. 121: 1883-1887. DOI: 10.1021/ja9827550 |
0.387 |
|
1999 |
Arvidsson PI, Davidsson O?, Hilmersson G. Enantioselective butylation of aliphatic aldehydes by mixed chiral lithium amide/n-BuLi dimers Tetrahedron Asymmetry. 10: 527-534. DOI: 10.1016/S0957-4166(99)00033-6 |
0.427 |
|
1999 |
Arvidsson PI, Davidsson O?, Hilmersson G. Enantioselective butylation of aliphatic aldehydes by mixed chiral lithium amide/n-BuLi dimers Tetrahedron Asymmetry. 10: 527-534. DOI: 10.1016/S0957-4166(99)00033-6 |
0.527 |
|
1999 |
Arvidsson PI, Hilmersson G, Davidsson Ö. Rational Design of Chiral Lithium Amides for Asymmetric Alkylation Reactions-NMR Spectroscopic Studies of Mixed Lithium Amide/Alkyllithium Complexes Chemistry - a European Journal. 5: 2348-2355. DOI: 10.1002/(SICI)1521-3765(19990802)5:8<2348::AID-CHEM2348>3.0.CO;2-A |
0.423 |
|
1999 |
Arvidsson PI, Hilmersson G, Davidsson O. Rational design of chiral lithium amides for asymmetric alkylation reactions - NMR spectroscopic studies of mixed lithium amide/alkyllithium complexes Chemistry - a European Journal. 5: 2348-2355. DOI: 10.1002/(Sici)1521-3765(19990802)5:8<2348::Aid-Chem2348>3.0.Co;2-A |
0.518 |
|
1999 |
Arvidsson PI, Ahlberg P, Hilmersson G. Intraaggregate fluxional lithium and carbanion exchanges in a chiral lithium amide/n-butyllithium mixed tetramer directly observed by multinuclear NMR Chemistry - a European Journal. 5: 1348-1354. DOI: 10.1002/(Sici)1521-3765(19990401)5:4<1348::Aid-Chem1348>3.0.Co;2-L |
0.654 |
|
1999 |
Arvidsson PI, Ahlberg P, Hilmersson G. Intraaggregate fluxional lithium and carbanion exchanges in a chiral lithium amide/n-butyllithium mixed tetramer directly observed by multinuclear NMR Chemistry - a European Journal. 5: 1348-1354. DOI: 10.1002/(SICI)1521-3765(19990401)5:4<1348::AID-CHEM1348>3.0.CO;2-L |
0.402 |
|
1999 |
Arvidsson PI, Hilmersson G, Davidsson O. Rational design of chiral lithium amides for asymmetric alkylation reactions - NMR spectroscopic studies of mixed lithium amide/alkyllithium complexes Chemistry - a European Journal. 5: 2348-2355. |
0.423 |
|
1998 |
Kang J, Santamaria J, Hilmersson G, Rebek J. J. Self-assembled molecular capsule catalyzes a diels-alder reaction [22] Journal of the American Chemical Society. 120: 7389-7390. DOI: 10.1021/Ja980927N |
0.305 |
|
1998 |
Kang J, Hilmersson G, Santamaría J, Rebek J. Diels - Alder reactions through reversible encapsulation Journal of the American Chemical Society. 120: 3650-3656. DOI: 10.1021/Ja973898+ |
0.343 |
|
1998 |
Tokunaga Y, Rudkevich DM, Santamaría J, Hilmersson G, Rebek J. Solvent controls synthesis and properties of supramolecular structures Chemistry - a European Journal. 4: 1449-1457. DOI: 10.1002/(Sici)1521-3765(19980807)4:8<1449::Aid-Chem1449>3.0.Co;2-Y |
0.307 |
|
1998 |
Hilmersson G, Rebek J. Coupling of molecular motions through non-bonding interactions: 13C NMR spin-lattice relaxation studies of a host-guest complex Magnetic Resonance in Chemistry. 36: 663-669. DOI: 10.1002/(Sici)1097-458X(199809)36:9<663::Aid-Omr350>3.0.Co;2-1 |
0.307 |
|
1997 |
Hilmersson G, Arvidsson PI, Davidsson O, Håkansson M. Chiral lithium amide/solute complexes: X-ray crystallographic and NMR spectroscopic studies Organometallics. 16: 3352-3362. DOI: 10.1021/Om960989R |
0.438 |
|
1997 |
Ahlberg P, Karlsson A, Davidsson O?, Hilmersson G, Löwendahl M. Mechanism and solvent catalysis of the degenerate 1,12-metalations of [1.1]ferrocenophanyllithium and [1.1]ferrocenophanylsodium studied by NMR spectroscopy Journal of the American Chemical Society. 119: 1751-1757. DOI: 10.1021/Ja964346E |
0.536 |
|
1997 |
Ahlberg P, Davidsson O, Löwendahl M, Hilmersson G, Karlsson A, Håkansson M. Structure of [1.1]ferrocenophanyllithium in the solution and the solid state. Absence of an intramolecular [C-H-C]- hydrogen bond Journal of the American Chemical Society. 119: 1745-1750. DOI: 10.1021/Ja9619519 |
0.554 |
|
1997 |
Karlsson A, Hilmersson G, Ahlberg P. Iron diprotonated [1.1] ferrocenophane generated in super-acid and directly observed by NMR spectroscopy Journal of Physical Organic Chemistry. 10: 590-592. DOI: 10.1002/(Sici)1099-1395(199707)10:7<590::Aid-Poc919>3.0.Co;2-M |
0.495 |
|
1996 |
Hilmersson G, Ahlberg P, Davidsson O?. Enantiomeric perturbation of equilibria. Differential solvation of a chiral lithium amide by the enantiomers of 2-methyltetrahydrofuran measured by NMR spectroscopy Journal of the American Chemical Society. 118: 3539-3540. DOI: 10.1021/Ja9540740 |
0.595 |
|
1996 |
Hilmersson G, Ahlberg P, Davidsson O?. Enantiomeric perturbation of equilibria. Differential solvation of a chiral lithium amide by the enantiomers of 2-methyltetrahydrofuran measured by NMR spectroscopy Journal of the American Chemical Society. 118: 3539-3540. DOI: 10.1021/ja9540740 |
0.302 |
|
1996 |
Karlsson A, Löwendahl M, Hilmersson G, Davidsson O, Ahlberg P. [1.1 ]Ferrocenophanes in solution - Anti or syn isomers? Journal of Physical Organic Chemistry. 9: 436-438. |
0.415 |
|
1995 |
Hilmersson G, Davidsson O. Solution structure of a key intermediate used in asymmetric alkylation reactions. 1H, 1H-NOESY and 6Li, 1H-HOESY studies of mixtures of a chiral lithium amide and n-butyllithium Journal of Organometallic Chemistry. 489: 175-179. DOI: 10.1016/0022-328X(94)05157-7 |
0.493 |
|
1995 |
Hilmersson G, Davidsson O?. A multinuclear NMR study of a chiral lithium amide with an intramolecular chelating methoxy group in coordinating solvents at the slow ligand exchange limit The Journal of Organic Chemistry. 60: 7660-7669. |
0.368 |
|
1995 |
Hilmersson G, Davidsson O?. A multinuclear NMR study of a chiral lithium amide with an intramolecular chelating methoxy group in coordinating solvents at the slow ligand exchange limit The Journal of Organic Chemistry. 60: 7660-7669. |
0.368 |
|
1995 |
Hilmersson G, Davidsson O. Stereogenic lithium centers in a complex between n-butyllithium and a dilithiated chiral amine: Solution studies by 6Li, 1H-HOESY, 6Li,6Li-COSY, and 6Li,6Li-EXSY NMR Organometallics. 14: 912-918. |
0.348 |
|
1995 |
Hilmersson G, Davidsson O. Stereogenic lithium centers in a complex between n-butyllithium and a dilithiated chiral amine: Solution studies by 6Li, 1H-HOESY, 6Li,6Li-COSY, and 6Li,6Li-EXSY NMR Organometallics. 14: 912-918. |
0.348 |
|
1995 |
Hilmersson G, Davidsson O. Solution structure of a key intermediate used in asymmetric alkylation reactions. 1H, 1H-NOESY and 6Li, 1H-HOESY studies of mixtures of a chiral lithium amide and n-butyllithium Journal of Organometallic Chemistry. 489: 175-179. |
0.308 |
|
1994 |
Ahlberg P, Davidsson O, Hilmersson G, Löwendahl M, Håkansson M. Crystal structure of ferrocenophanyllithium: Absence of an intramolecular C-H⋯-C hydrogen bond Journal of the Chemical Society, Chemical Communications. 1573-1574. DOI: 10.1039/C39940001573 |
0.525 |
|
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