Covering: 2015. Previous review: Nat. Prod. Rep., 2016, 33, 382–431 This review covers the
literature published in 2015 for marine natural products (MNPs), with 1220 citations (792 for …

This review covers the literature published in 2015 for marine natural products (MNPs), with
1220 citations (792 for the period January to December 2015) referring to compounds …

The implementation of ortho-quinone methide (o-QM) intermediates in complex molecule
assembly represents a remarkably efficient strategy designed by Nature and utilized by …

Covering: 2011 to July 2017. Spiroketal (spiroacetal), a common moiety in numerous natural
products, drugs and functional molecules, has been a central topic in organic chemistry for a …

A new Ag/Brønsted acid co-catalyzed spiroketalization of β-alkynyl ketones with para-
quinone methides (p-QMs) has been established, enabling multiple C–C and C–O bond …

Herein presented is a review of the reactivity and synthetic utility of ortho-quinone methides
and ortho-quinone methide imines. These versatile intermediates have received significant …

Generation of reactive intermediates and interception of these fleeting species under
physiological conditions is a common strategy employed by Nature to build molecular …

Penilactones A and B consist of a γ-butyrolactone and two clavatol moieties. We identified
two separate gene clusters for the biosynthesis of these key building blocks in Penicillium …

Herein, we introduce an iodonium ylide strategy to achieve novel α-alkylation of cyclic 1, 3-
dicarbonyls through harnessing C (sp3)–Rh species generated from 5-exo-trig cyclization to …

The spiroketal moiety is an important privileged scaffold that occurs extensively in natural
products, drugs, and bioactive molecules. Naturally occurring spiroketals are numerous …