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For comprehensive reviews, see
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For comprehensive reviews, see:
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Acemoglu L., and Williams J.M.J. de Meijere, A., Assoc. Ed. In: Negishi E.-i. (Ed). Handbook of Organopalladium Chemistry for Organic Synthesis Vol. 2 (2002), J. Wiley & Sons, New York, NY 1689 Chapter. V2.1.2
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Acemoglu, L.1
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Moreno-Manas M., and Pleixats R. de Meijere, A., Assoc. Ed. In: Negishi E.-i. (Ed). Handbook of Organopalladium Chemistry for Organic Synthesis Vol. 2 (2002), J. Wiley & Sons, New York, NY 1707 Chapter. V.2.1.3
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Courillon C., Thorimbert S., and Malacria M. de Meijere, A., Assoc. Ed. In: Negishi E.-i. (Ed). Handbook of Organopalladium Chemistry for Organic Synthesis Vol. 2 (2002), J. Wiley & Sons, New York, NY 1795 Chapter V.2.1.5
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Trost B.M., and Verhoeven T.R. In: Wilkinson G., Stone F.G.A., and Abel E.W. (Eds). Comprehensive Organometallic Chemistry Vol. 8 (1982), Pergamon, Oxford 799
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Trost, B.M.1
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70449404821
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For review articles on catalytic asymmetric allylation with π-allyl palladium complexes, see
-
For review articles on catalytic asymmetric allylation with π-allyl palladium complexes, see:
-
-
-
-
17
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0003445429
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Jacobsen E.N., Pfaltz A., and Yamamoto H. (Eds), Springer, Heidelberg
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Pfaltz A., and Lautens M. In: Jacobsen E.N., Pfaltz A., and Yamamoto H. (Eds). Comprehensive Asymmetric Catalysis (2000), Springer, Heidelberg 833
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Pfaltz, A.1
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Trost, B.M.1
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21
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33846933027
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A review article on the use of Iridium complexes for asymmetric allylation reactions:
-
A review article on the use of Iridium complexes for asymmetric allylation reactions:. Helmchen G., Dahnz A., Dubon P., Schelwies M., and Weihofen R. Chem. Commun. (2007) 675
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Helmchen, G.1
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70449401457
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For review articles, see
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For review articles, see:
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24
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de Meijere, A., Assoc. Ed. Negishi E.-i. (Ed), J. Wiley & Sons, New York, NY Chapter V.2.1.4
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Negishi E.-i., and Liou S.-Y. de Meijere, A., Assoc. Ed. In: Negishi E.-i. (Ed). Handbook of Organopalladium Chemistry for Organic Synthesis Vol. 2 (2002), J. Wiley & Sons, New York, NY 1769 Chapter V.2.1.4
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42
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70449431260
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Unpublished results
-
Unpublished results.
-
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43
-
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4544291065
-
-
For the isolation and structure elucidation of Abyssomicin, see:
-
For the isolation and structure elucidation of Abyssomicin, see:. Bister B., Bishoff D., Strobele M., Riedlinger J., Reicke A., Wolter F., Bull A.T., Zahner H., Fiedler H.P., and Sussmuth R.D. Angew. Chem., Int. Ed. 43 (2004) 2574
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Bister, B.1
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Zahner, H.8
Fiedler, H.P.9
Sussmuth, R.D.10
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44
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63849306648
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For a review article on the synthetic approaches to Abyssomicin, see:
-
For a review article on the synthetic approaches to Abyssomicin, see:. Nicolaou K.C., Harrison S.T., and Chen J.S. Synthesis (2009) 33
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Synthesis
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Nicolaou, K.C.1
Harrison, S.T.2
Chen, J.S.3
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33749868637
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A review article on eliminations of π-allyl palladium derivatives:. de Meijere, A., Assoc. Ed.;. Negishi E.-i. (Ed), J. Wiley & Sons, New York, NY Chapter V.2.5.1
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A review article on eliminations of π-allyl palladium derivatives:. Shimizu I. de Meijere, A., Assoc. Ed.;. In: Negishi E.-i. (Ed). Handbook of Organopalladium Chemistry for Organic Synthesis Vol. 2 (2002), J. Wiley & Sons, New York, NY 1981 Chapter V.2.5.1
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Shimizu, I.1
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70449406851
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54
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70449421394
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For a recent application of double catalysis to a highly efficient asymmetric allylation of aldehydes, see
-
For a recent application of double catalysis to a highly efficient asymmetric allylation of aldehydes, see:
-
-
-
-
56
-
-
70449406853
-
-
See also Ref. 26
-
See also Ref. 26.
-
-
-
-
57
-
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70449401458
-
-
note
-
The relative stereochemistry was determined by NOESY experiment for compounds 26, 28, 30, 31, 42 and 43; stereochemistry of other cyclic products was assumed by analogy. The copies of spectra, along with schematic representations of the stereochemical correlations, can be found in the Supplementary data to this article.
-
-
-
-
59
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45549083295
-
-
Recently, a similar approach has been successfully applied in natural product synthesis:
-
Recently, a similar approach has been successfully applied in natural product synthesis:. Roulland E. Angew. Chem., Int. Ed. 47 (2008) 3762
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(2008)
Angew. Chem., Int. Ed.
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Roulland, E.1
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70449415995
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note
-
THF, acetonitrile, DMF, DMSO, nitromethane, N-methylpyrrolidone.
-
-
-
-
67
-
-
70449373176
-
-
note
-
Chloride, bromide, iodide, acetate, phenoxide, phosphate.
-
-
-
-
68
-
-
70449406852
-
-
note
-
Pyrrolidine, dimethylamine, diethylamine, dicyclohexylamine, diisopropylamine, hexamethyldisilazane, methyl cyclohexylamine, diphenylamine, methylaniline, chiral amines derived from proline, such as methoxymethylpyrrolidine, diphenylprolinol and its' TMS-ether.
-
-
-
-
69
-
-
70449384544
-
-
note
-
In addition to BINAP and axially chiral ligands mentioned in the text, chiral ferrocene based phosphane ligands and Box were also used.
-
-
-
-
70
-
-
65549099061
-
-
Recently, an interesting approach was described, where chiral aminophosphanes were used as both organocatalysts and ligands; however, enantioselectivities were modest:
-
Recently, an interesting approach was described, where chiral aminophosphanes were used as both organocatalysts and ligands; however, enantioselectivities were modest:. Sato T., and Tomioka K. Heterocycles 77 (2009) 587
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Heterocycles
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70449442462
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For description of the technique of dry-flash chromatography, see
-
For description of the technique of dry-flash chromatography, see:
-
-
-
-
73
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70449457957
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Textbook of Practical Organic Chemistry
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5th ed, London, New York, NY
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Vogel's1
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A recent account which includes some improvements of the separation technique: Pedersen, D. S.; Rosenbohm, C. Synthesis 2001, 2431.
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A recent account which includes some improvements of the separation technique: Pedersen, D. S.; Rosenbohm, C. Synthesis 2001, 2431.
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