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Walter Wever

Texas Tech University

18

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The GAP Chemistry for Chiral N-Phosphonyl Imine-Based Strecker Reaction.

2011 ChemInform
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New Multicomponent Domino Reactions (MDRs) in Water: Highly Chemo-, Regio- and Stereoselective Synthesis of Spiro{[1,3]dioxanopyridine}-4,6-diones and Pyrazolo[3,4-b]pyridines.

2011 ChemInform
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The GAP chemistry for chiral N-phosphonyl imine-based Strecker reaction

2011 Green Chemistry
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New multicomponent domino reactions (MDRs) in water: highly chemo-, regio- and stereoselective synthesis of spiro{[1,3]dioxanopyridine}-4,6-diones and pyrazolo[3,4-b]pyridines

2010 Green Chemistry
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Four-Component Domino Reaction Providing an Easy Access to Multifunctionalized Tricyclo[6.2.2.01.6]dodecane Derivatives.

2010 ChemInform
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Research Article: Asymmetric Hydrophosphylation of Chiral N‐Phosphonyl Imines Provides an Efficient Approach to Chiral α‐Amino Phosphonates

2010 Chemical Biology & Drug Design
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Asymmetric catalytic N-phosphonyl imine chemistry: the use of primary free amino acids and Et2AlCN for asymmetric catalytic Strecker reaction.

2010 Journal of Organic Chemistry
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Asymmetric hydrophosphylation of chiral N-phosphonyl imines provides an efficient approach to chiral α-amino phosphonates.

2010 Chemical Biology & Drug Design
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Research Article: Asymmetric Hydrophosphylation of Chiral N-Phosphonyl Imines Provides an Efficient Approach to Chiral α-Amino Phosphonates: Asymmetric Hydrophosphylation of Chiral N-Phosphonyl Imines

2010 Chemical Biology & Drug Design
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Asymmetric Catalytic N‐Phosphonyl Imine Chemistry: The Use of Primary Free Amino Acids and Et2AlCN for Asymmetric Catalytic Strecker Reaction.

2010 ChemInform
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