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Our Chem. Soc. Rev. Article! Radical Retrosynthesis: A Powerful Strategy for Modern Assembly of Terpenoid Natural Products. Modern radical chemistry—MHAT, RAE, XEC, photoredox, HAT—reshapes retrosynthetic logic for complex terpenoids. pubs.rsc.org/en/content/art…
Thrilled to share our progress on the synthesis of highly oxidized DMOA-derived meroterpenoids—now out in JACS:pubs.acs.org/doi/10.1021/ja…! The unexpected reaction we stumbled upon in the final step turned out to be especially fascinating.
#TotalSynthesis of DMOA-Derived Meroterpenoids: Achieving Selectivity in the Synthesis of (+)-Berkeleyacetal D and (+)-Peniciacetal I by Jianpeng Zhang, Xiaotong Luo, Jingfu Zhang, and Chao Li @LabChao in @J_A_C_S pubs.acs.org/doi/10.1021/ja…
Establishing the Comprehensive Structure-Activity Relationship of the Natural Antibiotic Kibdelomycin/Amycolamicin (Chao Li and co-workers) @LabChao onlinelibrary.wiley.com/doi/10.1002/an…
We're excited to have achieved a structure-activity relationship analysis of the complex natural antibiotics Kibdelomycin/Amycolamicin through total synthesis. We hope this work will contribute to the development of new antibiotic therapies. onlinelibrary.wiley.com/doi/10.1002/an…
The final version of this study was published today in @Nature : nature.com/articles/s4158…
Today we report in @ChemRxiv a scalable solution to the total synthesis (and structural reassignment) of the Portimines (bit.ly/3iJ61DT). In collaboration with @_chrisgparker_ and Luke Lairson the remarkable biological activity of this natural product family was revealed
Excited to share our latest paper on the total synthesis of Illicium sesquiterpenes. Not only access more targets but synthetically connect distinct molecular architectures of different subfamilies through late-stage skeletal reorganization triggered by Lewis acids or oxidants.
Divergent Total Syntheses of Illicium Sesquiterpenes through Late-Stage Skeletal Reorganization | Journal of the American Chemical Society @CHNSci @TotalSynthesis @TotalSyntheses #Divergent #TotalSynthesis #sesquiterpenes #Rearrangement #LateStage pubs.acs.org/doi/10.1021/ja…
pubs.acs.org
Divergent Total Syntheses of Illicium Sesquiterpenes through Late-Stage Skeletal Reorganization
We disclose unified, protecting-group-free, bioinspired divergent total syntheses of eight allo-cedrane and seco-prezizaane Illicium sesquiterpenes and formal syntheses of five anislactone sesquite...
Nickel-Catalyzed C-I-Selective C(sp2)-C(sp3) Cross-Electrophile Coupling of Bromo(iodo)arenes with Alkyl Bromides (Chao Li and co-workers) @LabChao onlinelibrary.wiley.com/doi/10.1002/an…
Hopefully, this recent work from our group will help some medicinal chemists. A general C(sp2)–I selective C(sp2)–C(sp3) cross-electrophile coupling. onlinelibrary.wiley.com/doi/10.1002/an…
Modern alchemy appearing today in @ScienceMagazine : science.org/doi/10.1126/sc… Commentary (thank you Prof. Ye!): science.org/doi/10.1126/sc…
Modern Alchemy with rAP. Appearing today in @ChemRxiv is a solution to the longstanding (>100 year) challenge of extending the scope of the original Kolbe reaction beyond simple hydrocarbons bearing no functional groups: bit.ly/3sBQ5Ve
Today we report in @ChemRxiv a scalable solution to the total synthesis (and structural reassignment) of the Portimines (bit.ly/3iJ61DT). In collaboration with @_chrisgparker_ and Luke Lairson the remarkable biological activity of this natural product family was revealed
Please check out our total synthesis of (−)-Peyssonnoside A @J_A_C_S. Big congratulations to Bo @BoXu44807071 and Chang! Catalysis-Enabled 13-Step Total Synthesis of (−)-Peyssonnoside A pubs.acs.org/doi/10.1021/ja…
pubs.acs.org
Catalysis-Enabled 13-Step Total Synthesis of (−)-Peyssonnoside A
We report a 13-step enantioselective and stereoselective total synthesis of (−)-peyssonnoside A, a unique diterpene glucoside with a rare and highly congested pentasubstituted cyclopropane and...
Congratulations to chemist Prof. Phil Baran, who has been awarded the 2022 Danisco Foundation Science Excellence Award from @IFF. Baran is recognized for advancing science and technology relevant to the future of food, nutrition, and health magazine.scripps.edu/awards-and-hon… @BaranLabReads
Final version of this study was published today in @J_A_C_S : bit.ly/3QGPDhP
Simple, practical, and broadly applicable. Next generation decarboxylative arylation, appearing today in @ChemRxiv : bit.ly/3z6Ko5Y
🎁Do you recognize this PhD student in front of his hood in 1999? There he started out to become a true artist in @TotalSynthesis. Birthday present: autobio of S. Kent l-i-c.org/1129, the artist of Total Synthesis of #Peptides/#Proteins & #NativeChemicalLigation. Cheers!
An atroposelective synthesis of Darobactin, appearing today in @ChemRxiv : bit.ly/3z9tJyC
Electroaffinity labeling: a powerful new tool for target identification and Chemical Biology. Appearing today in @ChemRxiv, a collaboration with brilliant @Merck scientists: bit.ly/3B5eSEv
#LCSOSynthesisProblem of the week! Elija challenged us with the synthesis of Amycolamicin and Kibdelomycin from @LabChao in @J_A_C_S ! #Totalsynthesis Take a look: epfl.ch/labs/lcso/wp-c… For original paper: pubs.acs.org/doi/pdf/10.102…
I am very glad to discover some new TEMPO chemistry in natural product synthesis!
Reductive Radical Annulation Strategy toward Bicyclo[3.2.1]octanes: Synthesis of ent-Kaurane and Beyerane Diterpenoids by Junming Zhuo, Chunlin Zhu, Jinbao Wu, Zijian Li, and Chao Li @LabChao in @J_A_C_S pubs.acs.org/doi/10.1021/ja…
So happy to finish this complex natural product!
Total Synthesis of the Potent and Broad-Spectrum Antibiotics Amycolamicin and Kibdelomycin @TotalSyntheses @Total_Synthesis #Synthesis #Antibioic #Broadspectrum #Amycolamicin #Kibdelomycin pubs.acs.org/doi/10.1021/ja…
#TotalSynthesis of the Potent and Broad-Spectrum Antibiotics Amycolamicin and Kibdelomycin by Shaoqiang Yang, Chenglong Chen, Jie Chen, and Chao Li @LabChao in @J_A_C_S pubs.acs.org/doi/10.1021/ja…
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