Late-stage diversification of natural products

B Hong, T Luo, X Lei - ACS central science, 2020 - ACS Publications
Late-stage diversification of natural products is an efficient way to generate natural product
derivatives for drug discovery and chemical biology. Benefiting from the development of site …

Recent advances in the synthesis of ent-kaurane diterpenoids

X Zhao, B Cacherat, Q Hu, D Ma - Natural Product Reports, 2022 - pubs.rsc.org
Covering: 2015 to 2020 The ent-kaurane diterpenoids are integral parts of tetracyclic natural
products that are widely distributed in terrestrial plants. These compounds have been found …

Selective functionalization of benzylic C (sp3)–H bonds to synthesize complex molecules

Y Zhang, T Zhang, S Das - Chem, 2022 - cell.com
Functionalization of the benzylic C (sp 3)–H bond has become a compelling and robust tool
to speed up pre-clinical research for" lead discovery." Besides bring frequently utilizated to …

Total synthesis of sculponin U through a photoinduced radical cascade cyclization

W Cao, Z Wang, Y Hao, T Wang… - Angewandte Chemie …, 2023 - Wiley Online Library
We have accomplished the total synthesis of sculponin U, a polycyclic C‐20‐oxygenated
kaurane diterpenoid featuring a 7, 20‐lactone‐hemiketal bridge, through a radical cascade …

Leveraging Nonstrained C–C Bonds for Selective Carboacylation of an Unactivated Alkyne via Transient Dearomatization

J He, T Cao, K Chen, S Zhu - Organic Letters, 2024 - ACS Publications
Carboacylation of an unsaturated bond represents a powerful transformation. However, only
a few examples of carboacylation of alkyne have been reported through C–C bond scission …

Total Syntheses of Diepoxy-ent-Kaurane Diterpenoids Enabled by a Bridgehead-Enone-Initiated Intramolecular Cycloaddition

Y Li, Q Xue, X Zhao, D Ma - Journal of the American Chemical …, 2024 - ACS Publications
Here, we report the enantioselective total syntheses of four diepoxy-ent-kaurane
diterpenoids including (−)-Macrocalin B,(−)-Acetyl-macrocalin B, and (−)-Isoadenolin A and …

Total synthesis of (−)-oridonin: an interrupted Nazarov approach

L Kong, F Su, H Yu, Z Jiang, Y Lu… - Journal of the American …, 2019 - ACS Publications
An enantioselective total synthesis of (−)-oridonin is accomplished based on a key
interrupted Nazarov reaction. The stereochemistry of the Nazarov/Hosomi–Sakurai cascade …

Catalytic Asymmetric Total Synthesis of (−)-Garryine via an Enantioselective Heck Reaction

C Li, F Lu, Y Cai, C Zhang, Y Shao… - Journal of the …, 2023 - ACS Publications
The first asymmetric total synthesis of the hexacyclic veatchine-type C20-diterpenoid
alkaloid (−)-garryine is presented. Key steps include a Pd-catalyzed enantioselective Heck …

Tetracyclic diterpenoid synthesis facilitated by ODI-cascade approaches to bicyclo [3.2. 1] octane skeletons

K Gao, J Hu, H Ding - Accounts of Chemical Research, 2021 - ACS Publications
Conspectus Tetracyclic diterpenoids (C20) mainly refer to the plant terpenoids bearing
biogenetically related carbon skeletons derived from copalyl diphosphates (ent-CPP and …

New strategies in the efficient total syntheses of polycyclic natural products

W Liu, B Hong, J Wang, X Lei - Accounts of Chemical Research, 2020 - ACS Publications
Conspectus Polycyclic natural products are an inexhaustible source of medicinal agents,
and their complex molecular architecture renders challenging synthetic targets where …