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For an excellent paper on combining one-pot, step reduction and atom economy in organic chemistry see:. Clarke P.A., Santos S., and Martin W.H.C. Green Chem. 9 (2007) 438
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For excellent reviews on organocatalytic domino reactions see:. Enders D., Grondal C., and Hüttl M.R.M. Angew. Chem., Int. Ed. 46 (2007) 1570
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For selected reviews on quaternary stereocenters see:. Christoffers J., and Mann A. Angew. Chem., Int. Ed. 40 (2001) 4591
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To the best of our knowledge, there are only a few previous recent examples of the formation of an all-carbon stereocenter in chiral amine-catalyzed domino reactions see: Ref. 5w and
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To the best of our knowledge, there are only a few previous recent examples of the formation of an all-carbon stereocenter in chiral amine-catalyzed domino reactions see: Ref. 5w and. Rios R., Sundén H., Vesely J., Zhao G.-L., Dziedzic P., and Córdova A. Adv. Synth. Catal. 349 (2007) 1028
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For an excellent review on organocatalytic Michael additions see:. Sulzer Mossé S., and Alexakis A. Chem. Commun. (2007) 3123
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57
-
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65549170994
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-
note
-
6Na) requires m/z 355.0901, found 355.0897.
-
-
-
-
58
-
-
21244473265
-
-
Similar effects have been observed in organocatalytic Mannich-type reactions see:
-
Similar effects have been observed in organocatalytic Mannich-type reactions see:. Westermann B., and Neuhaus C. Angew. Chem., Int. Ed. 44 (2005) 4077
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Westermann, B.1
Neuhaus, C.2
-
62
-
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65549101593
-
-
note
-
4Na) requires m/z 344.0660, found 344.0657.
-
-
-
-
63
-
-
65549087459
-
-
note
-
4Na) requires m/z 344.0660, found 344.0658.
-
-
-
-
64
-
-
65549154311
-
-
note
-
CCDC 704580 contains the supplementary crystallographic data for this Letter. These data can be obtained free of charge from The Cambridge Crystallographic Data Centre via www.ccdc.cam.ac.uk/data_request/cif.
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