Natural products (NPs) are important sources of clinical drugs due to their structural diversity
and biological prevalidation. However, the structural complexity of NPs leads to synthetic …

Conspectus Convergent synthesis strategies in which a target molecule is prepared by a
branched approach wherein two or more complex fragments are combined at a late stage …

Covering: 2011–2017 Radical cyclizations have a rich history in organic chemistry and have
been particularly generous to the field of natural product synthesis. Owing to their ability to …

Aplyviolene (1) and macfarlandinE (2, Scheme1A) are representative of the more complex
members of the rearranged spongian diterpene class of natural products.[1, 2] These …

Transition‐metal‐mediated cleavage of C− C single bonds can enable entirely new
retrosynthetic disconnections in the total synthesis of natural products. Given that C− C bond …

Covering: 1986 to 2020 Natural products are an enduring source of chemical information
useful for probing biologically relevant chemical space. Toward gathering further structure …

Natural products have had an immense influence on science and have directly led to the
introduction of many drugs. Organic chemistry, and its unique ability to tailor natural products …

The architecture and bioactivity of natural products frequently serve as embarkation points
for the exploration of biologically relevant chemical space. Total synthesis followed by …

The natural products of heterobranch molluscs display a huge variability both in structure
and in their bioactivity. Despite the considerable lack of information, it can be observed from …

The species diversity of marine heterobranch sea slugs found on field trips around Bunaken
Island (North Sulawesi, Indonesia) and adjacent islands of the Bunaken National Marine …