[4] Vartanyan S A, Banbanyan S O. Rearrangement of acetylenic compounds with participation of the π-electrons of the triple bond[J]. Russian Chemical Reviews.1967,36:670-673.
[5] Engel D A, Dudley G B. The Meyer-Schuster rearrangement for the synthesis of α,β-unsaturated carbonyl compounds[J]. Organic and Biomolecular Chemistry.2009,7(20);4149-4158
[6] Sugawara Y, Yamada W, Yoshida S, Ikeno T, Yamada T. Carbon dioxide-mediated catalytic rearrangement of propargyl alcohols into α,β-unsaturated ketones[J]. Journal of the American Chemical Society,2009,129;12902-12903
[7] Hongchao Zheng, Michal Lejkowski, Dennis G. Mild and selective boronic acid catalyzed 1,3-transpositon of allylic alcohols and Meyer-Schuster rearrangement of propargylic alcohols[J]. HallChem.2011,2;1305-1310
[8] Edens M.Boerner D. Chase C R. Nass D. Schiavelli M D. The mechanism of the Meyer-Schuster rearrangement[J]. The Journal of Organic Chemistry.1977.42:3403 3408.
[9] Andres J. Cardenas R. Silla E, Tapia O. A theoretical study of the Meyer-Schuster reaction mechanism: minimum-energy profile and properties of transition-state structure[J] Journal of the American Chemical Society.1988.110:666-674
[10] Tapia O. Lluch J M, Cardena R, Andres J. Theoretical study of salvation effects on chemical reactions. A combined quantum chemical/Monte Carlo study of the Meyer-Schuster reaction mechanism in water[J]. Journal of the American Chemical Society.1989,111:829-835
[11] 钟传蓉,卢爱,炔醇的应用与生产[J].油田化学,2000,17(3):285-288
[12] 李春颖,王佳,刘明婧等.氢氧化钠溶液中丙炔醇对铝的缓蚀作用及吸附热力学研究.表面技术,36(3):12-39
[13] Ting A, Schaus S E. Organocatalytic Asymmetric Mannich Reactions: New Methodology, Catalyst Design, and Synthetic Applications[J]. Eur J org Chem,2007:5797-5815
[14] 徐秀娟,陈光旭.芳香胺参加的Mannich反应[J]. 化学学报,1982,40(5):463-468.
[15] Manabe K, Kobayashi S. Mannich-type Reactions of Aldehydes, Amines, and Ketones in a Colloidal Dispersion System Created by a Bronsted Acid-surfactant-combined Catalyst in Water[J]. Org let,1999,1;1965-1967
[16] Seayad Jayasree, Tillack Anngeret ,Hartung Christian G, Beller Matthias. Base-catalyzed hydroamination of olefins: an environmentally friendly route to amines [J]. Advanced Synthesis &Catalysis.2002,344(8):795-813
[17] a) Brunet J, Neibecker D. Catalytic Hydroamination of Unsaturated Carbon-Carbon Bonds[J]. Catalytic Heterofunctionalization[J].2001,4:91-132; b) Roesky P W, Muller T E, Asymmetric Catalytic Hydroamination of Activated Olefins in lonic Liquids[J]. Angewandte. Chemic.2003,115:2812-2814.
[18] Casimir, J.R.; Turetta, C.; Ettouati,L.; Pairs, J. Tetrahedron Lett.1995,36,4797.
[19]Tiwari, A.K.; Nakamura, R. M.; Agawane, S.B.; Ali, A.Z.; Ku-mac,K.V. Bioorg.Med.Chem.Lett.2008,18,4130
[20] 严汉英.论β-氨基酮的药理活性[J]. 南药译丛,1962,3(372):63-64
[21] Nakib T A, Bezjak V K, Meegan M J. Synthesis and antifungal activity of some 3-benzylidenechroman-4-ones, 3-benzylidenethiochroman-4-ones and 2- benzyl-idene-1-tetrelones[J]. Eur. J. Med.Chem.1990,25:455
[22] Nakib T A. A new synthesis of [1]benzothiopyran[4,3-b]-pyridines and pyrans[J]. J. Med. Res.1988,1:10
[23] Shaoguang, S.; Qian, Z.; Qun, L.; Jing, K.; Yanbing, Y.; Dongwei, L.; Dewen, D Tetrahedron Lett 2005,46,6271
[24] Kamogawa H, Kuhota K, Nanasawa M. Bull Soc Jap,1970,51(5);1571
[25] 张传新,程铁明,李润涛. M(OTf)3催化IV-烷氧羰基吡咯或噻吩与甲醛和盐酸伯胺的新颖Mannich反应[J]. 化学学报,2002,60(3):481-486.
[26] 肖立伟,孔洁,周秋香,胡悦立. 聚苯乙烯负载氯化铁一锅法合成β-氨基酮类衍生物[J]. 应用化学学报,2014.06-0715-06 β-氨基酮类化合物文献综述和参考文献(3):http://www.youerw.com/wenxian/lunwen_80499.html