ΠŸΠΎΠΌΠΎΡ‰ΡŒ Π² написании студСнчСских Ρ€Π°Π±ΠΎΡ‚
АнтистрСссовый сСрвис

Π›ΠΈΡ‚Π΅Ρ€Π°Ρ‚ΡƒΡ€Π°. 
АлкилированиС Π΅Π½Π°ΠΌΠΈΠ½ΠΎΠ², Π΄ΠΈΠΊΠ΅Ρ‚ΠΎΠ½ΠΎΠ² ΠΈ Π΅Π½Π°ΠΌΠΈΠ½ΠΎΠΊΠ΅Ρ‚ΠΎΠ½ΠΎΠ²

Π Π΅Ρ„Π΅Ρ€Π°Ρ‚ΠŸΠΎΠΌΠΎΡ‰ΡŒ Π² Π½Π°ΠΏΠΈΡΠ°Π½ΠΈΠΈΠ£Π·Π½Π°Ρ‚ΡŒ ΡΡ‚ΠΎΠΈΠΌΠΎΡΡ‚ΡŒΠΌΠΎΠ΅ΠΉ Ρ€Π°Π±ΠΎΡ‚Ρ‹

T. Tiner-Harding, P. Mariano // Intramolecular photoarylations of N-(haloaryl)ethyl-Π²-enaminones. // J. Org. Chem., 1982, 47, 482βˆ’485. J. Whitesell, M. Whitesell // Alkylation of ketones and aldehydes via their nitrogen derivatives. // Synthesis, 1983, 7, 517βˆ’536. S. Lu, A. Lewin // Enamine-imine tautomerism in Π±, Π²-unsaturated Π±-amino acids. // Tetrahedron, 1998, 54, 15 097βˆ’15 014. A. Cook (ed… Π§ΠΈΡ‚Π°Ρ‚ΡŒ Π΅Ρ‰Ρ‘ >

Π›ΠΈΡ‚Π΅Ρ€Π°Ρ‚ΡƒΡ€Π°. АлкилированиС Π΅Π½Π°ΠΌΠΈΠ½ΠΎΠ², Π΄ΠΈΠΊΠ΅Ρ‚ΠΎΠ½ΠΎΠ² ΠΈ Π΅Π½Π°ΠΌΠΈΠ½ΠΎΠΊΠ΅Ρ‚ΠΎΠ½ΠΎΠ² (Ρ€Π΅Ρ„Π΅Ρ€Π°Ρ‚, курсовая, Π΄ΠΈΠΏΠ»ΠΎΠΌ, ΠΊΠΎΠ½Ρ‚Ρ€ΠΎΠ»ΡŒΠ½Π°Ρ)

S. Dyke // Chemistry of enamines. // Cambridge University Press, Cambridge, 1973.

A. Cook (ed) // Enamines: synthesis, structure and reactions. // Marcell Decker, New York, 1969.

I. Chaaban, J. Greenhill, M. Ramli // Reactions between enaminones and enones. Part 2. C versus N-alkylation with cyclohex-2-enone. Structure confirmation by reduction of a dienaminone derivative of a dehydrated dimedone dimer. // J. Chem. Soc. Perkin Trans., 1981, 1, 3120−3124.

J. Whitesell, M. Whitesell // Alkylation of ketones and aldehydes via their nitrogen derivatives. // Synthesis, 1983, 7, 517−536.

A. Zanina, S. Shergina, I. Sokolov, M. Shvartsberg // Alkylation of sterically hindered 1,3-diketones under phase-transfer conditions. // Russ. Chem. Bl., 1996, 45, 2389−2392 // Izv. Akad. Nauk Ser. Khim. 1996, 10, 2518−2521.

S. Lu, A. Lewin // Enamine-imine tautomerism in Π±, Π²-unsaturated Π±-amino acids. // Tetrahedron, 1998, 54, 15 097−15 014.

J. Henriksen, S. Hammerum // Heats of formation of imine and enamine radical cations and the corresponding neutral molecules // Int. J. Mass Spect, 1998 179/180, 301−308.

S. Caccamese, G Principato // Resolution of the enantiomers of tetrahydrozoline by chiral HPLC. The racemization of the enantiomers via an imine-enamine tautomerism. // Tetrahedron: Asymmetry, 1998, 9, 2939−2945.

M. Shimizu, A. Morita, T. Kaga // Double nucleophilic addition to Π±, Π²-unsaturated aldimines induced by titanium tetrahalides. // Tetrahedron Lett., 1999, 40, 8401−8405.

S. Knьppel, R. FrΡ†lich, G. Erker // Formation of functionalized [3]ferrocenophane derivatives by an enamine condensation reaction.// J. Organomet. Chem., 2000, 595, 308−312.

A. Tkachev, A. Rukavishnikov // Enaminones of the 2-acetylcyclopent-1-en-1-ylamine type derived from the terpenic compounds limonene, 3-carene and Π΄-cadinol. // Mendeleev Commun., 1992, 1, 161−162.

S. Popov, A. Tkachev // New chiral agents for resolution of racemic cis-permethric and cis-Z-cyhalothric acids. // Tetrahedron: Asymmetry, 1995, 6, 4, 1013−1018.

J. Greenhill, A. Moten // N-Alkylation of enaminones. // Tetrahedron, 1983, 39, 3405−3408.

A. Tkachev, S. Popov // Alkylation of enaminoketone with a modified carane skeleton. Formation of stable Π²-diketone monoimines. // Russ. J. Org. Chem., 1997, 33, 5, 601−606.

T. Tiner-Harding, P. Mariano // Intramolecular photoarylations of N-(haloaryl)ethyl-Π²-enaminones. // J. Org. Chem., 1982, 47, 482−485.

P. Bugler, I. Cottrell, C. Cowden, A. Davies, U. Dolling // An investigation into the alkylation of 1,2,4-triazole // Tetrahedron Lett., 2000, 41, 1297−1301.

ΠŸΠΎΠΊΠ°Π·Π°Ρ‚ΡŒ вСсь тСкст
Π—Π°ΠΏΠΎΠ»Π½ΠΈΡ‚ΡŒ Ρ„ΠΎΡ€ΠΌΡƒ Ρ‚Π΅ΠΊΡƒΡ‰Π΅ΠΉ Ρ€Π°Π±ΠΎΡ‚ΠΎΠΉ