Total synthesis of natural fregenedadiol and its diacetate, rearranged labdanes with aromatized B ring

Philkhana, Satish Chandra ; Reddy, D. Srinivasa (2017) Total synthesis of natural fregenedadiol and its diacetate, rearranged labdanes with aromatized B ring Tetrahedron Letters, 58 (13). pp. 1262-1264. ISSN 0040-4039

Full text not available from this repository.

Official URL: http://doi.org/10.1016/j.tetlet.2017.02.010

Related URL: http://dx.doi.org/10.1016/j.tetlet.2017.02.010

Abstract

Labdane based natural products are most abundant and widely distributed in nature with many compounds exhibiting exceptional biological properties. Fregenedadiol is a bicyclic diterpene isolated from Halimium viscosum and represents a new carbon skeleton fregenedane with its B ring aromatized. Here, we report a total synthesis of this interesting natural product using one-pot Diels-Alder/aromatization sequence and selective hydrogenolysis as key steps.

Item Type:Article
Source:Copyright of this article belongs to Elsevier B.V.
ID Code:121930
Deposited On:23 Jul 2021 08:29
Last Modified:30 Jul 2021 07:36

Repository Staff Only: item control page