C-alkylation of chiral tropane- and homotropane-derived enamines

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Abstract

The synthesis and alkylation of chiral, nonracemic tropane- and homotropane-derived enamines is examined as an approach to enantioenriched α-alkylated aldehydes. The two bicyclic N auxiliaries, which differ by a single methylene group, give opposite senses of asymmetric induction on alkylation with EtI and provide modestly enantioenriched 2-ethylhexanal (following hydrolysis of the alkylated iminium). The observed stereoselectivity is supported by density functional studies of ethylation for both enamines. © 2013 American Chemical Society.

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β-Keto Acids in Organic Synthesis

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CITATION STYLE

APA

Hodgson, D. M., Charlton, A., Paton, R. S., & Thompson, A. L. (2013). C-alkylation of chiral tropane- and homotropane-derived enamines. Journal of Organic Chemistry, 78(4), 1508–1518. https://doi.org/10.1021/jo3025972

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