Rujukan Enamina

  1. ↑ Clayden, Jonathan (2001). Organic chemistry. Oxford, Oxfordshire: Oxford University Press. ISBN 978-0-19-850346-0.
  2. ↑ Enamines: Synthesis: Structure, and Reactions, Second Edition, Gilbert Cook (Editor). 1988, Marcel Dekker, NY. ISBN 0-8247-7764-6
  3. ↑ Imines and Enamines | PharmaXChange.info
  4. ↑ Stork, Gilbert.; Brizzolara, A.; Landesman, H.; Szmuszkovicz, J.; Terrell, R. (1963). "The Enamine Alkylation and Acylation of Carbonyl Compounds". Journal of the American Chemical Society (dalam bahasa Inggeris). 85 (2): 207–222. doi:10.1021/ja00885a021. ISSN 0002-7863.
  5. ↑ Mannich, C.; Davidsen, H. (1936). "Über einfache Enamine mit tertiär gebundenem Stickstoff" [On simple enamines with triple-bonded nitrogen]. Berichte der Deutschen Chemischen Gesellschaft (A and B Series) (dalam bahasa Jerman). 69 (9): 2106–2112. doi:10.1002/cber.19360690921. ISSN 0365-9488.
  6. ↑ Capon, Brian; Wu, Zhen Ping (April 1990). "Comparison of the tautomerization and hydrolysis of some secondary and tertiary enamines". The Journal of Organic Chemistry. 55 (8): 2317–2324. doi:10.1021/jo00295a017.
  7. ↑ Lockner, James. "Stoichiometric Enamine Chemistry" (PDF). Baran Group, The Scripps Research Institute. Dicapai pada 26 November 2014.
  8. ↑ Farmer, Steven (2013-10-16). "Enamine Reactions". UC Davis Chem Wiki.
  9. ↑ Carlson, R; Nilsson, A (1984). "Improved Titanium Tetrachloride Procedure for Enamine Synthesis". Acta Chemica Scandinavica. 38B: 49–53. doi:10.3891/acta.chem.scand.38b-0049.
  10. ↑ Lockner, James. "Stoichiometric Enamine Chemistry" (PDF). Baran Group, The Scripps Research Institute. Dicapai pada 26 November 2014.
  11. ↑ White, William Andrew; Weingarten, Harold (January 1967). "A versatile new enamine synthesis". The Journal of Organic Chemistry. 32 (1): 213–214. doi:10.1021/jo01277a052.
  12. ↑ Wade, L.G. (1999). Organic Chemistry. Saddle River, NJ: Prentice Hall. m/s. 1019. ISBN 9780139227417.
  13. ↑ Farmer, Steven (2013-10-16). "Enamine Reactions". UC Davis Chem Wiki.
  14. ↑ Meyers, A. I.; Williams, Donald R. (August 1978). "Asymmetric alkylation of acyclic ketones via chiral metallo enamines. Effect of kinetic vs. thermodynamic metalations". The Journal of Organic Chemistry. 43 (16): 3245–3247. doi:10.1021/jo00410a034.
  15. ↑ Seufert, Walter; Eiffenberger, Franz (1979). "Zur Halogenierung von Enaminen — Darstellung von β-Halogen-iminium-halogeniden". Chemische Berichte. 112 (5): 1670–1676. doi:10.1002/cber.19791120517.
  16. ↑ Ito, Y; Konoike, T; Saegusa, T (1975). "Synthesis of 1,4-diketones by the reaction of silyl enol ether with silver oxide. Regiospecific formation of silver(I) enolate intermediates". Journal of the American Chemical Society. 97 (3): 649–651. doi:10.1021/ja00836a034.
  17. ↑ Jang, HY; Hong, JB; MacMillan, DWC (2007). "Enantioselective organocatalytic singly occupied molecular orbital activation: the enantioselective alpha-enolation of aldehydes" (PDF). J. Am. Chem. Soc. 129 (22): 7004–7005. doi:10.1021/ja0719428. PMID 17497866.
  18. ↑ Li, Q; Fan, A; Lu, Z; Cui, Y; Lin, W; Jia, Y (2010). "One-pot AgOAc-mediated synthesis of polysubstituted pyrroles from primary amines and aldehydes: application to the total synthesis of purpurone". Organic Letters. 12 (18): 4066–4069. doi:10.1021/ol101644g. PMID 20734981.
  19. ↑ Guo, Fenghai; Clift, Michael D.; Thomson, Regan J. (September 2012). "Oxidative Coupling of Enolates, Enol Silanes, and Enamines: Methods and Natural Product Synthesis". European Journal of Organic Chemistry. 2012 (26): 4881–4896. doi:10.1002/ejoc.201200665. PMC 3586739. PMID 23471479.
  20. ↑ List, Benjamin (2002). "Proline-catalyzed asymmetric reactions". Tetrahedron. 58 (28): 5573–5590. doi:10.1016/s0040-4020(02)00516-1.
  21. ↑ Bui, Tommy; Barbas (2000). "A proline-catalyzed asymmetric Robinson Annulation". Tetrahedron Letters. 41 (36): 6951–6954. doi:10.1016/s0040-4039(00)01180-1.
  22. ↑ Wiener, Jake. "Enantioselective Organic Catalysis:Non-MacMillan Approaches" (PDF). Diarkibkan daripada yang asal (PDF) pada 26 October 2017. Dicapai pada 29 November 2014.
  23. ↑ Hickmott, Peter (May 1982). "Enamines: Recent advances in synthetic, spectroscopic, mechanistic, and stereochemical aspects—II". Tetrahedron. 38 (23): 3363–3446. doi:10.1016/0040-4020(82)85027-8.
  24. ↑ Mayr, H. (2003). "Structure-Nucleophilicity Relationships for Enamines". Chem. Eur. J. 9 (10): 2209–18. doi:10.1002/chem.200204666. PMID 12772295.
  25. ↑ Hickmott, Peter (May 1982). "Enamines: Recent advances in synthetic, spectroscopic, mechanistic, and stereochemical aspects—II". Tetrahedron. 38 (23): 3363–3446. doi:10.1016/0040-4020(82)85027-8.
  26. ↑ Lockner, James. "Stoichiometric Enamine Chemistry" (PDF). Baran Group, The Scripps Research Institute. Dicapai pada 26 November 2014.

Rujukan

WikiPedia: Enamina http://www.scripps.edu/baran/images/grpmtgpdf/Lock... http://chemwiki.ucdavis.edu/Organic_Chemistry/Reac... http://pharmaxchange.info/press/2011/04/imines-and... https://onlinelibrary.wiley.com/doi/10.1002/cber.1... https://authors.library.caltech.edu/76937/2/ja0719... https://www.princeton.edu/chemistry/macmillan/grou... https://d-nb.info/gnd/4152121-3 https://id.ndl.go.jp/auth/ndlna/00561928 https://pubs.acs.org/doi/abs/10.1021/ja00885a021 https://archive.org/details/organicchemistry00clay...