| Literature DB >> 21516168 |
Gary A Molander1, Frédéric Cadoret.
Abstract
We describe herein our progress toward the synthesis of halicyclamine A, which possesses very interesting biological activities and has never been synthesized. For this purpose, we proposed a stereoselective Diels-Alder reaction as a key step for the establishment of the stereogenic triad of the bis(piperidinyl) core of this molecule. A series of NMR studies was then conducted to establish the correct stereochemical assignment subsequent to the Diels-Alder reaction.Entities:
Year: 2011 PMID: 21516168 PMCID: PMC3079922 DOI: 10.1016/j.tetlet.2010.11.162
Source DB: PubMed Journal: Tetrahedron Lett ISSN: 0040-4039 Impact factor: 2.415