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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 …
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 …
Selective functionalization of benzylic C (sp3)–H bonds to synthesize complex molecules
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 …
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 …
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 …
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 …
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 …
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 …
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 …
biogenetically related carbon skeletons derived from copalyl diphosphates (ent-CPP and …
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 …