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Caine, D., Science of Synthesis, (2006) 8, 516..
Enantioselective Synthesis of Lithium Enolates by Deprotonation of Prochiral Ketones with Chiral, Nonracemic Lithium Amide Bases
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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]
Mahrwald, R.; Schetter, B., Science of Synthesis, (2008) 36, 849..
Additions to Lithium Enolates
,
Science of Synthesis
Seebach, Dieter; Beck, Albert K.; Capone, Stefania; Deniau, Gildas; Grošelj, Uroš; Zass, Engelbert, Synthesis 2009, 1-32.
Enantioselective Preparation of &bgr;²-Amino Acid Derivatives for &bgr;-Peptide Synthesis
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Synthesis
[DOI: 10.1055/s-0028-1087490]
Ljungdahl, Natalie; Pera, Núria Parera; Andersson, Kristian H. O.; Kann, Nina, Synlett 2008, 394-398.
The Development of an Asymmetric Nicholas Reaction Using Chiral Phosphoramidite Ligands
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Synlett
[DOI: 10.1055/s-2008-1032059]
Burtoloso, Antonio C. B., Synlett 2009, 320-327.
Catalytic Enantioselective α-Arylation of Carbonyl Compounds
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Synlett
[DOI: 10.1055/s-0028-1087673]
Nemoto, Tetsuhiro; Tsuruda, Kazuki; Yoshida, Mariko; Kono, Masato; Hamada, Yasumasa, Synthesis 2015, 47, 3914-3924.
Diastereoselective Synthesis of Trisubstituted Cyclopropanes by Palladium-Catalyzed Intramolecular Allylic Alkylation of ?-Aryl Esters?
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Synthesis
[DOI: 10.1055/s-0035-1560658]
Guizzetti, Stefania; Benaglia, Maurizio; Biaggi, Cinzia; Celentano, Giuseppe, Synlett 2010, 134-136.
A Convenient, Highly Stereoselective, Metal-Free Synthesis of Chiral Amines
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Synlett
[DOI: 10.1055/s-0029-1218541]
Gu, Zhenhua; Herrmann, Aaron T.; Stivala, Craig E.; Zakarian, Armen, Synlett 2010, 1717-1722.
Stereoselective Construction of Adjacent Quaternary Chiral Centers by the Ireland&endash;Claisen Rearrangement: Stereoselection with Esters of Cyclic Alcohols
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Synlett
[DOI: 10.1055/s-0029-1219965]
List, Benjamin; Mandrelli, Francesca.
Catalytic Asymmetric Synthesis of C2-Symmetric Secondary Amines
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Synfacts 2017, 13, 206
[DOI: 10.1055/s-0036-1589863]