Transition metal-catalysed C–H activation has emerged as an increasingly powerful platform
for molecular syntheses, enabling applications to natural product syntheses, late-stage …

Over the past few decades, the advent of C–H activation has led to a rethink among
chemists about the synthetic strategies employed for multi-step transformations. Indeed …

In this review, recent examples featuring C–H functionalization in the synthesis of complex
natural products are discussed. A focus is given to the way in which C–H functionalization …

The advent of modern C–H functionalization chemistries has enabled medicinal chemists to
consider a synthetic strategy, late stage functionalization (LSF), which utilizes the C–H …

The oxidation of unactivated C–H bonds has emerged as an effective tactic in natural
product synthesis and has altered how chemists approach the synthesis of complex …

The pool of abundant chiral terpene building blocks (ie,“chiral pool terpenes”) has long
served as a starting point for the chemical synthesis of complex natural products, including …

C–H functionalization is a very active research field that has attracted the interest of
scientists from many disciplines. This Outlook describes the collaborative efforts within the …

Detailed herein are our synthesis studies of longiborneol and related natural products. Our
overarching goals of utilizing a “camphor first” strategy enabled by skeletal remodeling of …

The widespread use of transition‐metal‐mediated C− H bond activation has altered the field
of organic synthesis. Notwithstanding the immense effect this strategy has had on classical …

A novel enantioselective palladium‐catalyzed dearomative cyclization has been developed
for the efficient construction of a series of chiral phenanthrenone derivatives bearing an all …