Results
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Zhou Li.
Evolution of chiral Lewis basic N-formamide as highly effective organocatalyst for asymmetric reduction of both ketones and ketimines with an unprecedented substrate scope
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Chemical Communications, 2007
[DOI: 10.1039/b703307a]
A NADPH-dependent (S)-imine reductase (SIR) from Streptomyces sp. GF3546 for asymmetric synthesis of optically active amines: purification, characterization, gene cloning, and expression
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Applied Microbiology and Biotechnology
[DOI: 10.1007/s00253-012-4629-4]
Oishi, M., Science of Synthesis, (2004) 7, 314..
Addition to Imines and Nitriles
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Science of Synthesis
Abbaspour Tehrani, K.; De Kimpe, N., Science of Synthesis, (2004) 27, 262..
With N,N-Bis(dichloroaluminio)aniline
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Science of Synthesis
O'Connor, J. M., Science of Synthesis, (2001) 1, 705..
Asymmetric Hydrogenation of Imines
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Science of Synthesis
Rendler, Sebastian; Oestreich, Martin, Synthesis 2005, 1727-1747.
Hypervalent Silicon as a Reactive Site in Selective Bond-Forming Processes
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Synthesis
[DOI: 10.1055/s-2005-869949]
Orito, Yuya; Nakajima, Makoto, Synthesis 2006, 1391-1401.
Lewis Base Catalyzed Asymmetric Reactions Involving Hypervalent Silicate Intermediates
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Synthesis
[DOI: 10.1055/s-2006-926405]
Korich, Andrew L.; Hughes, Thomas S., Synlett 2007, 2602-2604.
A Facile, One-Pot Procedure for Forming Diarylimines from Nitroarenes and Benzaldehydes
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Synlett
[DOI: 10.1055/s-2007-986668]
Collier, S. J., Science of Synthesis, (2007) 33, 477..
Direct Borylation of Imines (or Enamines)
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Science of Synthesis
Collier, S. J., Science of Synthesis, (2007) 33, 453..
Direct Silylation of Imines or Enamines
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Science of Synthesis
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