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J Org Chem ; 80(20): 10294-8, 2015 Oct 16.
Article in English | MEDLINE | ID: mdl-26402510

ABSTRACT

N-Boc (S)-proline was converted into (2S)-2-[(phenylselanyl)methyl]pyrrolidine, which was alkylated on nitrogen with 2-bromo-1-(4-methoxyphenyl)ethan-1-one. Reaction with vinyllithium, 6-exo-trig radical cyclization (Bu3SnH, AIBN, PhMe, 110 °C), dehydration (P2O5, H3PO4), and demethylation (BBr3) gave (+)-ipalbidine with ee >99%.


Subject(s)
Amines/chemistry , Free Radicals/chemistry , Indolizines/chemical synthesis , Proline/chemistry , Pyrrolidines/chemical synthesis , Alkylation , Cyclization , Ethane/analogs & derivatives , Ethane/chemistry , Indolizines/chemistry , Molecular Structure , Organoselenium Compounds , Pyrrolidines/chemistry , Stereoisomerism
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