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- W2912269371 abstract "Abstract The conjugate addition of enantiopure lithium N‐benzyl‐N‐(amethylbenzyl) amide to α,β unsaturated esters and amides displays high diastereoselectivity with extremely wide substrate scope and thus this process has been recognized as one of the most robust and reliable methods to prepare β‐amino acid derivatives. This methodology has found numerous applications, including in the areas of target synthesis and molecular recognition phenomena. Several chemoselective deprotection methods for removal of the N‐protecting groups have been developed. In order to expand the structural diversity of the accessible β‐amino acid derivatives, α‐functionalisation of the β‐amino ester has been investigated. α‐Functionalisation of the β‐amino acid derivatives can be achieved via elaboration of the intermediate enolate resulting from conjugate addition of a lithium amide reagent to an α,β‐unsaturated ester with an electrophile (tandem manner). This conjugate addition will continuously contribute not only to the area of amino acid/peptide chemistry but also in the areas of natural products and pharmaceutically important target syntheses." @default.
- W2912269371 created "2019-02-21" @default.
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- W2912269371 date "2020-04-29" @default.
- W2912269371 modified "2023-10-14" @default.
- W2912269371 title "Discussion Addendum for: Lithium Amides as Homochiral Ammonia Equivalents for Conjugate Additions to α,β‐Unsaturated Esters: Asymmetric Synthesis of ( <i>S</i> )‐ β‐Leucine" @default.
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- W2912269371 doi "https://doi.org/10.1002/0471264229.os096.04" @default.
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