Issue 9, 2017

Enabling syntheses of diterpenoid alkaloids and related diterpenes by an oxidative dearomatization/Diels–Alder cycloaddition strategy

Abstract

Covering: 2015 to March 2017

ortho-Benzoquinones generated from dearomatization of aromatic compounds are highly reactive intermediates in organic synthesis. One of their most important applications involves the participation in Diels–Alder cycloadditions, facilitating rapid access to molecular complexity. This powerful strategy has recently been utilized in the syntheses of diverse diterpenoid alkaloids and their biogenetically relevant diterpenes, which is the subject of this Highlight.

Graphical abstract: Enabling syntheses of diterpenoid alkaloids and related diterpenes by an oxidative dearomatization/Diels–Alder cycloaddition strategy

Article information

Article type
Highlight
Submitted
25 May 2017
First published
11 Aug 2017

Nat. Prod. Rep., 2017,34, 1044-1050

Enabling syntheses of diterpenoid alkaloids and related diterpenes by an oxidative dearomatization/Diels–Alder cycloaddition strategy

X. Liu and Y. Qin, Nat. Prod. Rep., 2017, 34, 1044 DOI: 10.1039/C7NP00033B

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