Article ID | Journal | Published Year | Pages | File Type |
---|---|---|---|---|
5281663 | Tetrahedron Letters | 2008 | 5 Pages |
Abstract
This Letter reports new and efficient synthetic approaches for biologically interesting cannabinoid analogues. The key strategies involve ethylenediamine diacetate/triethylamine-catalyzed cyclization. As an application of this methodology, one-step synthesis of biologically active natural (â)-hexahydrocannabinol and its unnatural enantiomer (+)-hexahydrocannabinol was carried out.
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Related Topics
Physical Sciences and Engineering
Chemistry
Organic Chemistry
Authors
Yong Rok Lee, Likai Xia,