| Literature DB >> 18642833 |
Susumu Tsuchida1, Atsunori Kaneshige, Tokutaro Ogata, Hiromi Baba, Yasutomo Yamamoto, Kiyoshi Tomioka.
Abstract
Consecutive cyclization of allylaminoalkenes by tandem aminolithiation-carbolithiation proceeded smoothly by using a lithium amide as a lithiating agent as well as protonating agent to give bicyclic amines, octahydroindolizine and hexahydro-1 H-pyrrolizine, in reasonably high yield and diastereoselectivity.Entities:
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Year: 2008 PMID: 18642833 DOI: 10.1021/ol801397v
Source DB: PubMed Journal: Org Lett ISSN: 1523-7052 Impact factor: 6.005