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1
-
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84871450966
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-
note
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Synthetic procedures and spectral data of the free ligand compounds 1 - 38 as well as complete tables containing complexations shifts and dispersion effects are collected in the Supplementary Data file.
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-
-
-
2
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0028144275
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1H NMR spectroscopy in the presence of a chiral dirhodium complex
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1H NMR spectroscopy in the presence of a chiral dirhodium complex. Tetrahedron: Asymmetry, 5, 27-30.
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(a) Díaz Gómez E, Albert D, Duddeck H, Kozhushkov SI, de Meijere A. (2006) Enantiodifferentiation of aliphatic ethers by the dirhodium method. European Journal of Organic Chemistry, 2278-2280;
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13C complexation shifts in the adduct formation of 2-butyl phenyl ethers with a dirhodium tetracarboxylate complex. Magnetic Resonance in Chemistry, 46, 23-29;
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Díaz Gómez, E.1
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(d) Duddeck H, Díaz Gómez E. (2009) Chiral recognition of ethers by NMR spectroscopy (mini review). Chirality, 21, 51-68.
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Díaz Gómez, E.1
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Chiral lanthanide shift reagents
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(a) Sullivan GR. (1978) Chiral lanthanide shift reagents. Topics in Stereochemistry, 10, 287-329;
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Sullivan, G.R.1
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(b) Rinaldi PL. (1983) The determination of absolute configuration using nuclear magnetic resonance techniques. Progress in NMR Spectroscopy, 15, 291-352;
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(c) Parker D. (1991) NMR determination of enantiomeric purity. Chemical Reviews, 91, 1441-1457;
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Rothchild, R.1
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Highly enantioselective rhodium-catalyzed hydrognation of 2-(2-methoxy-2-oxoethyl)acrylic acid - A convenient access of enantiomerically pure isoprenoid building blocks
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For example: (a)
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For example: (a) Ostermeier M, Brunner B, Korff C, Helmchen G. (2003) Highly enantioselective rhodium-catalyzed hydrognation of 2-(2-methoxy-2- oxoethyl)acrylic acid - A convenient access of enantiomerically pure isoprenoid building blocks. European Journal of Organic Chemistry, 3453-3459;
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Ostermeier, M.1
Brunner, B.2
Korff, C.3
Helmchen, G.4
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15
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0346366647
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Total synthesis of (+)-xyloketal D, a secondary metabolite from the mangrove fungus Xylaria sp.
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DOI 10.1016/j.tetlet.2003.10.189
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(b) Krohn K, Riaz M. (2004) Total synthesis of (+)-xyloketal D, a secondary metabolite from the mangrove fungus Xylaria sp. Tetrahedron Letters, 45, 293-294. (Pubitemid 37542264)
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Krohn, K.1
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Asymmetric synthesis of chiral Roche ester and its derivatives via Rh-catalyzed enantioselective hydrogenation with chiral phosphine- phosphoramidite ligands
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For recent papers see for example
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For recent papers see for example: (a) Qiu M, Wang D-Y, Hu X-P, Huang J-D, Yu S-B, Deng J, Duan Z-C, Zheng Z. (2009) Asymmetric synthesis of chiral Roche ester and its derivatives via Rh-catalyzed enantioselective hydrogenation with chiral phosphine-phosphoramidite ligands. Tetrahedron: Asymmetry, 20, 210-213;
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Qiu, M.1
Wang, D.-Y.2
Hu, X.-P.3
Huang, J.-D.4
Yu, S.-B.5
Deng, J.6
Duan, Z.-C.7
Zheng, Z.8
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17
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49049096215
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Asymmetric synthesis of the Roche ester and its derivatives by rhodium-INDOLPHOS-catalyzed hydrogenation
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(b) Wassenaar J, Kuil M, Reek JNH. (2008) Asymmetric synthesis of the Roche ester and its derivatives by rhodium-INDOLPHOS-catalyzed hydrogenation. Advanced Synthesis and Catalysis, 350, 1610-1614.
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Wassenaar, J.1
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Reek, J.N.H.3
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18
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Selective pyrolysis of bifunctional compounds: Gas-phase elimination of carbonate-ester functionalities
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Al-Azemi TF, Dib HH, Al-Awadi NA, El-Dusouqui OME. (2008) Selective pyrolysis of bifunctional compounds: gas-phase elimination of carbonate-ester functionalities. Tetrahedron, 64, 4126-4134.
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Al-Azemi, T.F.1
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Al-Awadi, N.A.3
El-Dusouqui, O.M.E.4
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19
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0037007629
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Synthetic studies on callipeltin A: Stereoselective synthesis of (2R,3R,4S)-3-hydroxy-2,4,6-trimethylheptanoic acid
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DOI 10.1016/S0957-4166(02)00178-7, PII S0957416602001787
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Zampella A, Sorgente M, D'Auria MV. (2002) Synthetic studies on callipeltin A: stereoselective synthesis of (2R,3R,4S)-3-hydroxy-2,4,6- trimethylheptanoic acid. Tetrahedron: Asymmetry, 13, 681-685. (Pubitemid 34597027)
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Zampella, A.1
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Density functional calculations (B3LYP 6-31G*) using SPARTAN '08 version 1.0.0, Wave function Inc., Irvine, CA; see also
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Dachsel, H.29
Doerksen, R.J.30
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Lee, A.M.42
Lee, M.S.43
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Nair, N.46
Peters, B.47
Proynov, E.I.48
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Rhee, Y.M.50
Ritchie, J.51
Rosta, E.52
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Simmonett, A.C.54
Subotnik, J.E.55
Woodcock III, H.L.56
Zhang, W.57
Bell, A.T.58
Chakraborty, A.K.59
Chipman, D.M.60
Keil, F.J.61
Warshel, A.62
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