Recent advances in the total synthesis of cyclobutane-containing natural products

J Li, K Gao, M Bian, H Ding - Organic Chemistry Frontiers, 2020 - pubs.rsc.org
Complex natural products bearing strained cyclobutane subunits, including terpenoids,
alkaloids and steroids, not only display fascinating architectures, but also show potent …

Natural product syntheses via carbonylative cyclizations

K Ma, BS Martin, X Yin, M Dai - Natural product reports, 2019 - pubs.rsc.org
Covering: 2000–2018 In this review, we highlight recent examples of natural product total
syntheses employing transition metal-mediated/catalyzed carbonylative cyclization …

Switching between the [2π+ 2σ] and Hetero‐[4π+ 2σ] Cycloaddition Reactivity of Bicyclobutanes with Lewis Acid Catalysts Enables the Synthesis of Spirocycles and …

JJ Wang, L Tang, Y Xiao, WB Wu, G Wang… - Angewandte …, 2024 - Wiley Online Library
The exploration of the complex chemical diversity of bicyclo [n. 1.1] alkanes and their use as
benzene bioisosteres has garnered significant attention over the past two decades …

syn-Selective Difunctionalization of Bicyclobutanes Enabled by Photoredox-Mediated C–S σ-Bond Scission

H Wang, JE Erchinger, M Lenz, S Dutta… - Journal of the …, 2023 - ACS Publications
Given the importance of cyclic frameworks in molecular scaffolds and drug discovery, it is
intriguing to precisely forge and manipulate ring systems in synthetic chemistry. In this field …

Stereoselective synthesis of cyclobutanes by contraction of pyrrolidines

C Hui, L Brieger, C Strohmann… - Journal of the American …, 2021 - ACS Publications
Here we report a contractive synthesis of multisubstituted cyclobutanes containing multiple
stereocenters from readily accessible pyrrolidines using iodonitrene chemistry. Mediated by …

Sesterterpenoids: chemistry, biology, and biosynthesis

K Li, KR Gustafson - Natural Product Reports, 2021 - pubs.rsc.org
Covering: July 2012 to December 2019 Over the last seven years, expanding research
efforts focused on sesterterpenoids has led to the isolation, identification, and …

Total Synthesis of Daphniphyllum Alkaloids: From Bicycles to Diversified Caged Structures

LD Guo, Y Chen, J Xu - Accounts of Chemical Research, 2020 - ACS Publications
Conspectus Native to the Asia-Pacific region and widely applied in traditional Chinese
medicine, the genus Daphniphyllum has produced over 330 known Daphniphyllum …

Two Terpenoid Derivatives with Different 3/5/6/6/5‐Fused Pentacyclic Skeletons from Hedyosmum orientale

YY Fan, CY Zheng, B Zhou, FM Zimbres… - Chinese Journal of …, 2023 - Wiley Online Library
Comprehensive Summary Chemical investigation of Hedyosmum orientale led to the
identification of two terpenoid derivatives, dyosmunoids A and B (1 and 2) featuring two …

Total Synthesis of the Diterpenes (+)-Randainin D and (+)-Barekoxide via Photoredox-Catalyzed Deoxygenative Allylation

O Vyhivskyi, O Baudoin - Journal of the American Chemical …, 2024 - ACS Publications
We report the first enantioselective total synthesis of diterpenoid randainin D, which
possesses a hydroazulenone core with a β-substituted butenolide moiety on the …

Unprecedented sesterterpenoids, orientanoids A–C: discovery, bioinspired total synthesis and antitumor immunity

CY Zheng, JX Zhao, CH Yuan, X Peng, M Geng… - Chemical …, 2023 - pubs.rsc.org
Sesterterpenoids are a very rare class of important natural products. Three new skeletal
spiro sesterterpenoids, named orientanoids A–C (1–3), were isolated from Hedyosmum …