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Oxygen linker 1a:
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Oxygen linker 1a:. Matsunaga S., Das J., Roels J., Vogl E.M., Yamamoto N., Iida T., Yamaguchi K., and Shibasaki M. J. Am. Chem. Soc. 122 (2000) 2252
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Sulfur linker 1c:
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Sulfur linker 1c:. Kumagai N., Matsunaga S., Kinoshita T., Harada S., Okada S., Sakamoto S., Yamaguchi K., and Shibasaki M. J. Am. Chem. Soc. 125 (2003) 2169
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Nitrogen linker 1d:
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Nitrogen linker 1d:. Majima K., Takita R., Okada A., Ohshima T., and Shibasaki M. J. Am. Chem. Soc. 125 (2003) 15837
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23
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33646086659
-
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note
-
For the synthesis of linked-BINOL 1a, see [3a]. Linked-BINOL 1a is also commercially available from Wako Pure Chemical Industries, Ltd. Catalog No. for (S,S)-1a, No. 152-02431; and for (R,R)-1a, No. 155-02421.
-
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Kolb, H.C.1
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10844266525
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For a review on catalytic asymmetric Mannich-type reaction, see:. Jacobsen E.N., Pfaltz A., and Yamamoto H. (Eds), Springer, Berlin Supplement 1, (Chapter 29.5)
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For a review on catalytic asymmetric Mannich-type reaction, see:. Kobayashi S., and Ueno M. In: Jacobsen E.N., Pfaltz A., and Yamamoto H. (Eds). Comprehensive Asymmetric Catalysis (2003), Springer, Berlin 143 Supplement 1, (Chapter 29.5)
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For selected other examples of direct Mannich-type reactions using metal catalysts: ketones as donors. Yamasaki S., Iida T., and Shibasaki M. Tetrahedron Lett. 40 (1999) 307
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0035825097
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For selected other examples of direct Mannich reactions using unmodified ketone and/or aldehyde as donors with organocatalysts
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For selected other examples of direct Mannich reactions using unmodified ketone and/or aldehyde as donors with organocatalysts,. Notz W., Sakthivel K., Bui T., Zhong G., and Barbas III C.F. Tetrahedron Lett. 42 (2001) 199
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Use of diphenylphosphinoyl imine is favorable because removal of protective group is relatively easy. A review for the use of diphenylphosphinoyl imines 2 in organic synthesis:
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Use of diphenylphosphinoyl imine is favorable because removal of protective group is relatively easy. A review for the use of diphenylphosphinoyl imines 2 in organic synthesis:. Weinreb S.M., and Orr R.K. Synthesis (2005) 1205
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Weinreb, S.M.1
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For selected recent related examples using conformationally flexible biphenyl unit in asymmetric catalysis, see
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For exceptional examples in Mannich-type reactions using readily enolizable substrates with oxidation state of carboxylic acid, see [23d,23e,24i,24j].
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For recent examples in asymmetric aldol reactions:
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For recent examples in asymmetric aldol reactions:. Evans D.A., Downey C.W., and Hubbs J.L. J. Am. Chem. Soc. 125 (2003) 8706
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For application of N-acylpyrrole as a donor after conversion into enol silane, see:. Evans D.A., and Johnson D.S. Org. Lett. 1 (1999) 595
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Use of an α,β-unsaturated N-acylpyrrole as an electrophile:. Matsunaga S., Kinoshita T., Okada S., Harada S., and Shibasaki M. J. Am. Chem. Soc. 126 (2004) 7559
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