參考文獻 |
1. Johnson, A. W.; LaCount, R. B., The Chemistry of Ylids. VI. Dimethylsulfonium Fluorenylide—A Synthesis of Epoxides1. J. Am. Chem. Soc. 1961, 83 (2), 417-423.
2. Corey, E. J.; Chaykovsky, M., Dimethyloxosulfonium methylide ((CH3)2SOCH2) and dimethylsulfonium methylide ((CH3)2SCH2). Formation and application to organic synthesis. J. Am. Chem. Soc. 1965, 87 (6), 1353-1364.
3. Aggarwal, V. K.; Bae, I.; Lee, H. Y.; Richardson, J.; Williams, D. T., Sulfur‐Ylide‐Mediated Synthesis of Functionalized and Trisubstituted Epoxides with High Enantioselectivity; Application to the Synthesis of CDP‐840. Angew. Chem., Int. Ed. 2003, 42 (28), 3274-3278.
4. Deng, X.-M.; Cai, P.; Ye, S.; Sun, X.-L.; Liao, W.-W.; Li, K.; Tang, Y.; Wu, Y.-D.; Dai, L.-X., Enantioselective synthesis of vinylcyclopropanes and vinylepoxides mediated by camphor-derived sulfur ylides: rationale of enantioselectivity, scope, and limitation. J. Am. Chem. Soc. 2006, 128 (30), 9730-9740.
5. Duan, Y.; Zhou, B.; Lin, J.-H.; Xiao, J.-C., Diastereoselective Johnson–Corey–Chaykovsky trifluoroethylidenation. Chem. Commun. 2015, 51 (66), 13127-13130.
6. Bernard, A. M.; Frongia, A.; Piras, P. P.; Secci, F.; Spiga, M., Regioselective synthesis of trisubstituted 2,3-dihydrofurans from donor− acceptor cyclopropanes or from reaction of the corey ylide with α-sulfenyl-, α-sulfinyl-, or α-sulfonylenones. Org. Lett. 2005, 7 (21), 4565-4568.
7. Zheng, J.-C.; Zhu, C.-Y.; Sun, X.-L.; Tang, Y.; Dai, L.-X., Highly Diastereoselective and Enantioselective Formal [4+1] Ylide Annulation for the Synthesis of Optically Active Dihydrofurans. J. Org. Chem. 2008, 73 (17), 6909−6912.
8. Lu, L.-Q.; Cao, Y.-J.; Liu, X.-P.; An, J.; Yao, C.-J.; Ming, Z.-H.; Xiao, W.-J., A new entry to cascade organocatalysis: reactions of stable sulfur ylides and nitroolefins sequentially catalyzed by thiourea and DMAP. J. Am. Chem. Soc. 2008, 130 (22), 6946-6948.
9. Cheng, B.-Y.; Wang, Y.-N.; Li, T.-R.; Lu, L.-Q.; Xiao, W.-J., Synthesis of polysubstituted pyrroles through a formal [4+1] cycloaddition/E1cb elimination/aromatization sequence of sulfur ylides and α,β-unsaturated imines. J. Org. Chem. 2017, 82 (23), 12134-12140.
10. Zhu, C.; Ding, Y.; Ye, L.-W., Ylide formal [4+1] annulation. Org. Biomol. Chem. 2015, 13 (9), 2530-2536.
11. Payne, G. B., Cyclopropanes from reactions of ethyl dimethylsulfuranylideneacetate with α,β-unsaturated compounds. J. Org. Chem. 1967, 32 (11), 3351-3355.
12. Clagett, M.; Gooch, A.; Graham, P.; Holy, N.; Mains, B.; Strunk, J., Organocopper intermediates. Synthesis of 2-isoxazoline N-oxides and cyclopropanes. J. Org. Chem. 1976, 41 (25), 4033-4035.
13. Chagarovsky, A. O.; Budynina, E. M.; Ivanova, O. A.; Villemson, E. V.; Rybakov, V. B.; Trushkov, I. V.; Melnikov, M. Y., Reaction of Corey ylide with α,β-unsaturated ketones: tuning of chemoselectivity toward dihydrofuran synthesis. Org. Lett. 2014, 16 (11), 2830-2833.
14. Liu, Y.-Q.; Li, Q.-Z.; Zhu, H.-P.; Feng, X.; Peng, C.; Huang, W.; Li, J.-L.; Han, B., Direct sulfide-catalyzed diastereoselective [4+1] annulations of ortho-Quinone Methides and bromides. J. Org. Chem. 2018, 83 (20), 12753-12762.
15. Zhang, Y.; Yu, A.; Jia, J.; Ma, S.; Li, K.; Wei, Y.; Meng, X., NaH promoted [4+3] annulation of crotonate-derived sulfur ylides with thioaurones: synthesis of 2,5-dihydrobenzo [4,5] thieno [3,2-b] oxepines. Chem. Commun. 2017, 53 (77), 10672-10675.
16. Chen, J.; Jia, P.; Huang, Y., Divergent Domino Reactions of Sulfur Ylides: Access to Functionalized Six-and Seven-Membered Nitrogen–Heterocycles. Org. Lett. 2018, 20 (21), 6715-6718.
17. Wu, H.-Y.; Chang, C.-W.; Chein, R.-J., Enantioselective Synthesis of (Thiolan-2-yl) diphenylmethanol and Its Application in Asymmetric, Catalytic Sulfur Ylide-Mediated Epoxidation. J. Org. Chem. 2013, 78 (11), 5788-5793.
18. Huang, M.-T.; Wu, H.-Y.; Chein, R.-J., Enantioselective synthesis of diaryl aziridines using tetrahydrothiophene-based chiral sulfides as organocatalysts. Chem. Commun. 2014, 50 (9), 1101-1103.
19. Wang, S.-H.; Chein, R.-J., (Thiolan-2-yl) diphenylmethyl benzyl ether/N,N′-diarylurea cocatalyzed asymmetric aziridination of cinnamyl bromide and aryl aldimine. Tetrahedron 2016, 72 (21), 2607-2615.
20. 郭昱成, 「以手性有機硫催化劑進行不對稱環丙烷化反應之研究與新型手性呋喃化合物開發」, 國立中正大學, 2017.
21. Wang, S.; Xu, L.; Lu, Y.-T.; Liu, Y.-F.; Han, B.; Liu, T.; Tang, J.; Li, J.; Wu, J.; Li, J.-Y., Discovery of benzofuran-3 (2H)-one derivatives as novel DRAK2 inhibitors that protect islet β-cells from apoptosis. Eur. J. Med. Chem. 2017, 130, 195-208.
22. Rong, Z. Q.; Wang, M.; Chow, C. H. E.; Zhao, Y., A Catalyst‐Enabled Diastereodivergent Aza‐Diels–Alder Reaction: Complementarity of N‐Heterocyclic Carbenes and Chiral Amines. Chem. - Eur. J. 2016, 22 (28), 9483-9487.
23. Clergue, S.; Rousseau, O.; Delaunay, T.; Dequirez, G.; Tran, T. V.; El Aakchioui, S.; Barozzino‐Consiglio, G.; Robiette, R., Asymmetric Sulfur‐Ylide‐Mediated Formal [4+1]‐Annulation Reaction: Scope and Mechanism. Chem. - Eur. J. 2018, 24 (44), 11417-11425.
24. King, L. C.; Ostrum, G. K., Selective Bromination with copper (II) bromide. J. Org. Chem. 1964, 29 (12), 3459-3461.
25. Wang, Z.-P.; He, Y.; Shao, P.-L., Transition-metal-free synthesis of polysubstituted pyrrole derivatives via cyclization of methyl isocyanoacetate with aurone analogues. Org. Biomol. Chem. 2018, 16 (30), 5422-5426.
26. Kafle, A.; Bhattarai, S.; Handy, S. T., An Unusual Triazole Synthesis from Aurones. Synthesis 2020, 52 (16), 2337-2346.
27. Taylor, K. M.; Taylor, Z. E.; Handy, S. T., Rapid synthesis of aurones under mild conditions using a combination of microwaves and deep eutectic solvents. Tetrahedron Lett. 2017, 58 (3), 240-241.
28. Morimoto, M.; Fukumoto, H.; Nozoe, T.; Hagiwara, A.; Komai, K., Synthesis and insect antifeedant activity of aurones against Spodoptera litura larvae. J. Agric. Food Chem. 2007, 55 (3), 700-705.
29. Manjulatha, K.; Srinivas, S.; Mulakayala, N.; Rambabu, D.; Prabhakar, M.; Arunasree, K. M.; Alvala, M.; Rao, M. B.; Pal, M., Ethylenediamine diacetate (EDDA) mediated synthesis of aurones under ultrasound: Their evaluation as inhibitors of SIRT1. Bioorg. Med. Chem. Lett. 2012, 22 (19), 6160-6165.
30. Varma, R. S.; Varma, M., Alumina-mediated condensation. A simple synthesis of aurones. Tetrahedron Lett. 1992, 33 (40), 5937-5940.
31. Carrasco, M. P.; Newton, A. S.; Gonçalves, L.; Góis, A.; Machado, M.; Gut, J.; Nogueira, F.; Hänscheid, T.; Guedes, R. C.; dos Santos, D. J., Probing the aurone scaffold against Plasmodium falciparum: design, synthesis and antimalarial activity. Eur. J. Med. Chem. 2014, 80, 523-534.
32. Fang, Q.-Y.; Yi, M.-H.; Wu, X.-X.; Zhao, L.-M., Regio-and Diastereoselective Spirocyclopropanation of Benzofuran-Derived Azadienes through 1, 4-Addition-Induced Dearomatization Reaction under Mild Conditions. Org. Lett. 2020, 22 (13), 5266-5270.
33. Trost, B. M.; Zuo, Z., Highly Regio‐, Diastereo‐, and Enantioselective Synthesis of Tetrahydroazepines and Benzo [b] oxepines through Palladium‐Catalyzed [4+ 3] Cycloaddition Reactions. Angew. Chem., Int. Ed. 2020, 59 (3), 1243-1247. |