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Synthesis of quaternary ?-methyl ?-amino acids by asymmetric alkylation of pseudoephenamine alaninamide pivaldimine.


ABSTRACT: The utility of pseudoephenamine as a chiral auxiliary for the alkylative construction of quaternary ?-methyl ?-amino acids is demonstrated. The method is notable for the high diastereoselectivities of the alkylation reactions, for its versatility with respect to electrophilic substrate partners, and for its mild hydrolysis conditions, which provide ?-amino acids without salt contaminants. Alternatively, ?-amino esters can be obtained by direct alcoholysis.

SUBMITTER: Hugelshofer CL 

PROVIDER: S-EPMC3884032 | biostudies-literature | 2013 Jun

REPOSITORIES: biostudies-literature

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Synthesis of quaternary α-methyl α-amino acids by asymmetric alkylation of pseudoephenamine alaninamide pivaldimine.

Hugelshofer Cedric L CL   Mellem Kevin T KT   Myers Andrew G AG  

Organic letters 20130607 12


The utility of pseudoephenamine as a chiral auxiliary for the alkylative construction of quaternary α-methyl α-amino acids is demonstrated. The method is notable for the high diastereoselectivities of the alkylation reactions, for its versatility with respect to electrophilic substrate partners, and for its mild hydrolysis conditions, which provide α-amino acids without salt contaminants. Alternatively, α-amino esters can be obtained by direct alcoholysis. ...[more]

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