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Merck

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

The Journal of organic chemistry (2013-01-30)
David M Hodgson, Andrew Charlton, Robert S Paton, Amber L Thompson
要旨

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.

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Sigma-Aldrich
2-Ethylhexanal, 96%