Open Access
Issue
E3S Web Conf.
Volume 267, 2021
7th International Conference on Energy Science and Chemical Engineering (ICESCE 2021)
Article Number 02011
Number of page(s) 6
Section Environmental Chemistry Research and Chemical Preparation Process
DOI https://doi.org/10.1051/e3sconf/202126702011
Published online 04 June 2021
  1. Wenlai Fan and Michael C. Qian. Characterization of Aroma Comopounds of Chinese “Wulianhye” and “Jiannanchun” Liquors by Aroma Extract Dilution Analysis. Journal of Agricultural and Food Chemistry. 2006, 54, 7, 2695-2704. [Google Scholar]
  2. Zoran Radic, Natilie A. Pickering, Daniel C. Vellom, Shelley Camp, and Palmer Taylor. Three distinct domains in the cholinesterase molecule confer selectivity for acetyl- and butyrylcholinesterase inhibitors. Biochemistry. 1993, 32, 45, 12074-12084. [Google Scholar]
  3. Jana Maríkova, Aneta Ritomska, Jan Korabecny, Rozalie Perinova, Abdullah Al Mamun, Tomas Kucera, Eliska Kohelova, Daniela Hulcova, Tereza Kobrlova, Jirí Kunes, Lucie Novakova, and Lucie Cahlíkova*. Aromatic Esters of the Crinane Amaryllidaceae Alkaloid Ambelline as Selective Inhibitors of Butyrylcholinesterase. J. Nat. Prod., 2020, 83, 1359-1367. [Google Scholar]
  4. Michael O. Frederick, Mark A. Pietz, Douglas P. Kjell, Rachel N. Richey, Gregg A. Tharp, Taichiro Touge, Naota Yokoyama, Michio Kida, and Toshiyasu Matsuo. Development of a Leuckart-Wallach Reation in Flow for the synthesis of Abemaciclib. Organic Process Research&Development 2017, 21(9), 1447-1451. [Google Scholar]
  5. A. Lukasiewicz. A study of the mechanism of certain chemical reactions—I : The mechanism of the leuckart-wallach reaction and of the reduction of schiff bases by formic acid. Tetrahedron. 19, 1963, 1789-1799. [Google Scholar]
  6. William A. Kleschick, Charles T. Buse, and Clayton H. Heathcock. Stereoselection in the aldol condensation. J. Am. Chem. Soc. 1977, 99, 1, 247-248. [Google Scholar]
  7. Rusli Daik, W. James Feast, Andrei S. Batsanov and Judith A. K. Howard. Stereochemical outcome of McMurry coupling. New Journal of Chemistry. 1998, 22, 1047-1049. [Google Scholar]
  8. B. H. Liu, Z. P. Li A review: Hydrogen generation from borohydride hydrolysis reaction. Journal of Power Sources. 2009, 187, 527-534. [Google Scholar]
  9. M. Niyaz Khan. Suggested Improvement in the Ing-Manske Producedure and Gabriel Synthesis of Primary Amines: Kinetic Study on Alkaline Hydrolysis of N-Phthaloylglycine and Acid Hydrolysis of N-(o-Carbosybenzoyl)glycine in Aqueous Organic Solvents. The Journal of Organic Chemistry. 1996, 61, 23, 8063-8068. [Google Scholar]
  10. Yingze Cao, Xiaoyong Zhang, Lei Tao, Kan Li, Zhongxin Xue, Lin Feng, and Yen Wei. Mussel-Inspired Chemistry and Michael Addition Reaction for Efficient Oil/Water Separation. ACS Appl. Mater. Interfaces 2013, 5, 10, 4438–4442. [Google Scholar]
  11. (a) Name Reactions (A Collection of Detailed Reaction Mechanisms), Jie Jack Li, Diels–Alder reaction., page 211-212.(b) Gao, S.; Wang, Q.; Chen, C. J. Am. Chem. Soc., 2009, 131, 1410-1412.(c) Diels, O.; Alder, K. Ann., 1928, 460, 98-122. [Google Scholar]
  12. (a) Vilsmeier, A.; Haack, A. Ber., 1927, 60, 119–122. German chemists Anton Vilsmeier and Albrecht Haack discovered this recation in 1927.(b) Lancelot, J.-C.; Ladureé, D.; Robba, M. Chem. Pharm. Bull., 1985, 33, 3122–3128.(c) Name Reactions (A Collection of Detailed Reaction Mechanisms), Jie Jack Li, Vilsmeier-Haack reaction,page 615-616. [Google Scholar]

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