Article ID | Journal | Published Year | Pages | File Type |
---|---|---|---|---|
5217616 | Tetrahedron | 2014 | 6 Pages |
Abstract
An enantioselective synthesis of the macrolactone core of natural product Sch725674 was accomplished from furfural. Key reactions in assembly of the macrolactone are the use of furan as a but-2-ene-dione equivalent and ring closing metathesis.
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Related Topics
Physical Sciences and Engineering
Chemistry
Organic Chemistry
Authors
Sunil Kumar Sunnam, Kavirayani R. Prasad,