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 …
derivatives for drug discovery and chemical biology. Benefiting from the development of site …
Bioinspired skeletal reorganization approach for the synthesis of steroid natural products
Y Wang, J Gui - Accounts of Chemical Research, 2024 - ACS Publications
Conspectus Steroids, termed “keys to life” by Rupert Witzmann, have a wide variety of
biological activities, including anti-inflammatory, antishock, immunosuppressive, stress …
biological activities, including anti-inflammatory, antishock, immunosuppressive, stress …
Divergent Total Syntheses of Illicium Sesquiterpenes through Late-Stage Skeletal Reorganization
P Fu, T Liu, Y Shen, X Lei, T Xiao, P Chen… - Journal of the …, 2023 - ACS Publications
We disclose unified, protecting-group-free, bioinspired divergent total syntheses of eight allo-
cedrane and seco-prezizaane Illicium sesquiterpenes and formal syntheses of five …
cedrane and seco-prezizaane Illicium sesquiterpenes and formal syntheses of five …
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 …
kaurane diterpenoid featuring a 7, 20‐lactone‐hemiketal bridge, through a radical 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 …
alkaloid (−)-garryine is presented. Key steps include a Pd-catalyzed enantioselective Heck …
Total synthesis of (−)-Rhodomollanol A
J Gao, P Rao, K Xu, S Wang, Y Wu… - Journal of the American …, 2020 - ACS Publications
An asymmetric approach for the first total synthesis of (−)-rhodomollanol A, a highly oxidized
diterpenoid, is described. The efficient synthetic strategy features three key …
diterpenoid, is described. The efficient synthetic strategy features three key …
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 …
products that are widely distributed in terrestrial plants. These compounds have been found …
New strategies in the efficient total syntheses of polycyclic natural products
Conspectus Polycyclic natural products are an inexhaustible source of medicinal agents,
and their complex molecular architecture renders challenging synthetic targets where …
and their complex molecular architecture renders challenging synthetic targets where …
Natural product total synthesis using rearrangement reactions
L Chen, G Li, L Zu - Organic Chemistry Frontiers, 2022 - pubs.rsc.org
Total synthesis of natural products has been an important pursuit in chemical synthesis due
to their fascinating structural complexity and/or interesting biological activities. In most …
to their fascinating structural complexity and/or interesting biological activities. In most …
Controllable skeletal reorganizations in natural product synthesis
Z Zhang, X Qian, Y Gu, J Gui - Natural Product Reports, 2024 - pubs.rsc.org
Covering: 2016 to 2023The synthetic chemistry community is always in pursuit of efficient
routes to natural products. Among the many available general strategies, skeletal …
routes to natural products. Among the many available general strategies, skeletal …