(2-Ethylamino-5-acetamido)tropone (CAS 18188-69-7)
(2-Ethylamino-5-acetamido)tropone (CAS:
18188-69-7) has molecular formula C11H14N2O2 and molecular weight 206.24 g/mol. This compound has been the subject of numerous scientific investigations due to its structural features and practical utility in synthetic chemistry and industrial processes. View product details →
Product Background
This comprehensive research profile examines the scientific literature surrounding (2-Ethylamino-5-acetamido)tropone.
Key Research Findings
- For each substrate class, we elucidate the distinct activation modes enabled by two predominant organocatalytic strategies: nucleophilic amine catalysis and N-heterocyclic carbene
- Cephalotane-type diterpenoids, a class of natural products exclusively found in Cephalotaxus plants, are well known for their attractive structures and potent biological activities
Detailed Literature Analysis
Below are the top-ranked research papers for (2-Ethylamino-5-acetamido)tropone, presented with bibliographic details and scientific abstracts.
Synthetic Chemistry
1. Organocatalytic Strategies for Higher-Order Cycloadditions: A Review of Substrate Activation and Enantiocontrol.
The construction of complex chiral cyclic architectures, ubiquitous in bioactive natural products, represents a perennial pursuit in organic synthesis. Among the myriad of strategies, cycloaddition reactions are unparalleled in their ability to efficiently assemble such structures with high atom economy. While higher-order cycloadditions (involving
2. Four Cytochrome P450 Enzymes Mediate Oxidation Cascades in the Biosynthesis of Cephalotane-Type Diterpenoids.
Cephalotane-type diterpenoids, a class of natural products exclusively found in Cephalotaxus plants, are well known for their attractive structures and potent biological activities. However, their low natural abundance and intricate cage-like structures hinder their accessibility. Recently, the identification of a cephalotene synthase (CsCTS) has a
3. An Enantioselective Nucleophilic Aromatic
This work presents the first leaving-group-directed aminocatalytic enantioselective nucleophilic aromatic
4. Enantioselective Pd-Catalyzed Electrochemical Dearomative Allylation of Tropones: Construction of All-C Quaternary Stereocenters.
A Pd-catalyzed electroreductive enantioselective dearomatization of tropones is documented. High levels of chemoselectivity toward the formation of seven-membered ring ketones featuring a stereochemically controlled all-carbon α-stereocenter are successfully accomplished by means of a Tsuji-Trost-like process (24 examples, regioselectivity >25:1,
Other Research
5. Stereoselective
Metalloenamines, generated through α-deprotonation of
Conclusion
The research literature on (2-Ethylamino-5-acetamido)tropone demonstrates sustained scientific interest, with publications continuing through 0. The compound serves as an important building block in synthetic chemistry and has been explored for various applications. Researchers and industrial users can view detailed specifications or submit an inquiry for pricing and availability.
Data Sources: PubMed/MEDLINE, CrossRef. 5 papers analyzed. Last updated: 2026-05-25. This article is automatically generated from peer-reviewed research data.