Covering: 1925 to July 2023 Among the sesquiterpenoids with rich structural diversity and
potential bioactivities, lindenane sesquiterpenoids (LSs) possess a characteristic cis, trans …

Covering: 2012. Previous review: Nat. Prod. Rep. 2012, 29, 1334. This review covers the
isolation, structural determination, synthesis and chemical and microbiological …

We report the first total synthesis of bolivanine in a 14-step pathway involving the synthesis
of onoseriolide. Our synthesis features a palladium-catalyzed intramolecular …

Covering: July 2010 to August 2019. Previous review: Nat. Prod. Rep., 2011, 28, 594 The
review covers recent progress on the isolation, identification, bioactivity and biomimetic …

Asymmetric total synthesis of the dimeric diterpenoid hispidanin A was accomplished by non‐
catalytic Diels–Alder cycloaddition at room temperature. The synthesis relies on iron …

The asymmetric total synthesis of three lindenane sesquiterpenoid oligomers, shizukaol J,
trichloranoid C and trishizukaol A, has been accomplished concisely in 15, 16 and 18 …

A previously proposed triene of the lindenane skeleton was synthesized, characterized, and
identified as the common intermediate for the non‐enzymatic synthesis of natural lindenane …

The syntheses of members of a family of lindenane sesquiterpenoid [4+ 2] dimers led to the
total syntheses of sarcandrolide J and shizukaol D. Inspired by a modified biosynthetic …

Disesquiterpenoids are constructed by two sesquiterpenoid molecules, containing at least
30 carbons with various connection patterns, and numerous new skeletons have been …

The dimeric lindenane sesquiterpenoids are mainly isolated from the plants of
Chloranthaceae family. Structurally, they have a crowded molecular scaffold decorated with …