Long ago, as an REU student, I worked on these molecules and they were HARD. The project was ultimately abandoned but this group was able to make a member of the family! Really impressed! They even used a cycloisomerization! #chemtwitter https://t.co/LaLnGFqwTN
Asymmetric Total Synthesis of Pre-schisanartanin C.
Mentions
Extended reach
Total likes
Video views
Mentions per month
Dec 2019 – May 2023Where it's discussed
-
X / Twitter14 posts
-
YouTube2 videos
-
News2 articles
AI synopsis
What people are saying
The discussions reveal a positive attitude toward the article, with posts mentioning techniques like cyclopropanation and Stille coupling, and expressing admiration for the researchers’ achievements, which underscores their high interest and recognition of the study's scientific importance.
Most discussions express appreciation and admiration for the complexities of the synthesis, indicating general agreement with the significance of the work.
The majority of posts show high curiosity, referencing specific methods and expressing fascination, reflecting strong interest.
Many discussions detail the synthesis steps and acknowledge personal familiarity or previous work, showing moderate to deep engagement.
Some posts highlight the innovative techniques and the potential influence on future research, suggesting moderate impact.
Abstract in brief
- The paper details the enantioselective total synthesis of Preschisanartanin C, a potent nortriterpenoid with antihepatitis, antitumor, and anti-HIV properties, using advanced organic chemistry techniques.
- It highlights key steps such as a gold-catalyzed intramolecular cyclopropanation to create a bicyclo[6.10]nonane core and a sequence of reactions including Pd-catalyzed Stille coupling, Sharpless asymmetric dihydroxylation, and lactonization to construct the molecule's side chain.
- The methods developed not only enable synthesis of Preschisanartanin C but also open pathways for creating other related compounds with similar rigid bicyclic cores.]
Top posts
Most liked on X and BlueskyPre-schisanartanin Cの全合成 超大作ですね ぜひ合成研の論文紹介に Asymmetric Total Synthesis of Pre-schisanartanin C https://t.co/7gs55mHF3O
#Chemlearning #Organicsynthesis #Totalsynthesis An interesting.... Asymmetric Total Synthesis of Pre-schisanartanin C ...#cyclopropanation ...#asymmetric #Diels–Alder ...#Pd-catalyzed #Stille coupling ...#Sharpless #dihydroxylation ...#lactonization https://t.co/qTxLonSB5H
Peking大Zhen Yang先生。お家芸感ある骨格の化合物の全合成ですね。 #学ぶの論文紹介 Asymmetric Total Synthesis of Pre-schisanartanin C https://t.co/WW2ClJ8hBF
Just Published: Asymmetric Total Synthesis of Pre-schisanartanin C https://t.co/1yxYFSliKn
Asymmetric Total Synthesis of Pre-schisanartanin C https://t.co/UTu0LiSd4X
All mentions
Understanding the Mukaiyama Aldol Reaction in Organic Chemistry
The Mukaiyama aldol reaction is a Lewis acid-catalyzed addition of silyl enol ethers to carbonyl compounds, highlighting the reaction mechanism and key steps involved.
Takai Olefination Reaction Mechanism and Applications
The Takai Olefination is a chromiumII-mediated homologation of aldehydes with haloform, producing E-configured alkenes. It involves chromium chloride reacting with haloform and aldehyde, leading to a nucleophilic…
RT @MlnProf: #Chemlearning #Organicsynthesis #Totalsynthesis An interesting.... Asymmetric Total Synthesis of Pre-schisanartanin C ...#c…
#Chemlearning #Organicsynthesis #Totalsynthesis An interesting.... Asymmetric Total Synthesis of Pre-schisanartanin C ...#cyclopropanation ...#asymmetric #Diels–Alder ...#Pd-catalyzed #Stille coupling ...#Sharpless #dihydroxylation ...#lactonization https://t.co/qTxLonSB5H
RT @EurekaMag: Asymmetric Total Synthesis of Pre-schisanartanin C https://t.co/UTu0LiSd4X
RT @EurekaMag: Asymmetric Total Synthesis of Pre-schisanartanin C https://t.co/UTu0LiSd4X
Asymmetric Total Synthesis of Pre-schisanartanin C https://t.co/UTu0LiSd4X
Peking大Zhen Yang先生。お家芸感ある骨格の化合物の全合成ですね。 #学ぶの論文紹介 Asymmetric Total Synthesis of Pre-schisanartanin C https://t.co/WW2ClJ8hBF
RT @Phil_Knutson_: Long ago, as an REU student, I worked on these molecules and they were HARD. The project was ultimately abandoned but th…
Long ago, as an REU student, I worked on these molecules and they were HARD. The project was ultimately abandoned but this group was able to make a member of the family! Really impressed! They even used a cycloisomerization! #chemtwitter https://t.co/LaLnGFqwTN
Asymmetric Total Synthesis of Pre-schisanartanin C https://t.co/92gB1hZnhu
Asymmetric Total Synthesis of Pre-schisanartanin C https://t.co/418Nz7MLZS
RT @OrgChemRarikuma: Pre-schisanartanin Cの全合成 超大作ですね ぜひ合成研の論文紹介に Asymmetric Total Synthesis of Pre-schisanartanin C https://t.co/7gs55mHF3O
Pre-schisanartanin Cの全合成 超大作ですね ぜひ合成研の論文紹介に Asymmetric Total Synthesis of Pre-schisanartanin C https://t.co/7gs55mHF3O
Just Published: Asymmetric Total Synthesis of Pre-schisanartanin C https://t.co/1yxYFSliKn
PhD group work. Familiar with every step... Asymmetric Total Synthesis of Pre-schisanartanin C https://t.co/7Alzo2uj2J