Tetrahydroquinoline is one of the most important simple nitrogen heterocycles, being
widespread in nature and present in a broad variety of pharmacologically active …

Oxidative cyclizations are important transformations that occur widely during natural product
biosynthesis. The transformations from acyclic precursors to cyclized products can afford …

Covering: up to September 2015 Meroterpenoids are hybrid natural products that partially
originate from the terpenoid pathway. The meroterpenoids derived from fungi display quite …

Abstract The Diels–Alder reaction is one of the most powerful and widely used methods in
synthetic chemistry for the stereospecific construction of carbon–carbon bonds. Despite the …

Covering: 2012 to 2021 Cyclopropane attracts wide interests in the fields of synthetic and
pharmaceutical chemistry, and chemical biology because of its unique structural and …

Covering: up to July 2019 Terpene synthases (TSs) are responsible for generating much of
the structural diversity found in the superfamily of terpenoid natural products. These elegant …

Attachment of isoprene units to various acceptors by prenylation plays an important role in
primary and secondary metabolism of living organisms. Protein prenylation belongs to …

Conspectus The Diels–Alder reaction is well known as a concerted [4+ 2] cycloaddition
governed by the Woodward–Hoffmann rules. Since Prof. Otto Diels and his student Kurt …

Fungal hybrid terpenoid saccharides constitute a new and growing family of natural products
with significant biomedical and agricultural activities. One representative family is the …

Diaporisoindoles A (1) and B (2), two novel isoprenylisoindole alkaloids, and an unusual
diisoprenylisoindole dimer diaporisoindole C (3), together with a precursor tenellone C (4) …