The Theoretical Total Synthesis of an Aromatic Esters of the Crinane Amaryllidaceae Alkaloid Ambelline

Danyang Liu; Zhijian Zhou; Hao Liu

doi:10.1051/e3sconf/202126702011

All issues

Volume 267 (2021)

E3S Web Conf., 267 (2021) 02011

References

Open Access

Issue		E3S Web Conf. Volume 267, 2021 7^th 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

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]
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]
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]
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]
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]
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]
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]
B. H. Liu, Z. P. Li A review: Hydrogen generation from borohydride hydrolysis reaction. Journal of Power Sources. 2009, 187, 527-534. [Google Scholar]
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]
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]
(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]
(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]

Current usage metrics show cumulative count of Article Views (full-text article views including HTML views, PDF and ePub downloads, according to the available data) and Abstracts Views on Vision4Press platform.

Data correspond to usage on the plateform after 2015. The current usage metrics is available 48-96 hours after online publication and is updated daily on week days.

Initial download of the metrics may take a while.

[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]