| Article ID | Journal | Published Year | Pages | File Type |
|---|---|---|---|---|
| 5218788 | Tetrahedron | 2013 | 12 Pages |
Abstract
An enantiospecific total synthesis of indole alkaloids eburnamonine, aspidospermidine and quebrachamine is described from lactic acid. Synthesis of all three alkaloids is accomplished from a single chiral building block. Johnson-Claisen rearrangement of a chiral allyl alcohol is the main feature for the installation of the required quaternary centre.
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Related Topics
Physical Sciences and Engineering
Chemistry
Organic Chemistry
Authors
John Eugene Nidhiry, Kavirayani R. Prasad,