127102-62-9Relevant academic research and scientific papers
Total synthesis of proposed cephalosporolides H and i
Li, Jinshan,Zhao, Chuanfang,Liu, Jun,Du, Yuguo
, p. 3885 - 3889 (2015)
An efficient total synthesis toward spiroketal diastereomers of cephalosporolides H and I was achieved, respectively, taking advantage of intramolecular Wacker-type spiroketalization on the common olefin-containing dihydroxy-γ-lactone substrate. By compar
Identification and Enantiodivergent Synthesis of (5 Z,9 S)-Tetradec-5-en-9-olide, a Queen-Specific Volatile of the Termite Silvestritermes minutus
Machara, Ale?,K?ivánek, Jan,Dolej?ová, Klára,Havlí?ková, Jana,Bednárová, Lucie,Hanus, Robert,Majer, Pavel,Kyjaková, Pavlína
, p. 2266 - 2274 (2018)
The queens of social insects differ from sterile colony members in many aspects of their physiology. Besides adaptations linked with their specialization for reproduction and extended lifespan, the queens also invest in the maintenance of their reproducti
Enantiomeric Recognition of Organic Ammonium Salts by Chiral Dialkyl-, Dialkenyl-, and Tetramethyl-Substituted Pyridino-18-crown-6 and Tetramethyl-Substituted Bis-pyridino-18-crown-6 Ligands: Comparison of Temperature-Dependent 1H NMR and Empirical Force
Bradshaw, Jerald S.,Huszthy, Peter,McDaniel, Christopher W.,Zhu, Cheng Y.,Dalley, N. Kent,et al.
, p. 3129 - 3137 (2007/10/02)
Six new chiral pyridino-18-crown-6 and one chiral bis-pyridino-18-crown-6 ligands have been prepared.The pyridino-crowns contain either two isopropyl, two isobutyl, two (S)-sec-butyl, two benzyl, two 3-butenyl, or four methyl substituents on chiral macror
