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Rationalization of the mechanism and chemoselectivity of versatile Au-catalyzed reactions of diazoesters with allyl-functionalized sulfides, selenides, amines, or ethers by DFT
Gao C., Cao T., Kirillov A.M., Fang R., Yang L.
free ylide intermediate. With an allyl amine as the second reactant, the main pathway is a selective
Amine adducts of triallylborane as highly reactive allylborating agents for Cu(i)-catalyzed allylation of chiral sulfinylimines
Alexeev Michael S., Strelkova Tatiana V., Ilyin Michael M., Nelyubina Yulia V., Bespalov Ivan A., Medvedev Michael G., Khrustalev Victor N., Kuznetsov Nikolai Yu.
Convenient, atom-efficient allylation reagents with high selectivity and tunable reactivity
Application of New Efficient Hoveyda-Grubbs Catalysts Comprising an N→Ru Coordinate Bond in a Six-Membered Ring for the Synthesis of Natural Product-Like Cyclopenta[b]furo[2,3-c]pyrroles
Antonova A.S., Vinokurova M.A., Kumandin P.A., Merkulova N.L., Sinelshchikova A.A., Grigoriev M.S., Novikov R.A., Kouznetsov V.V., Polyanskii K.B., Zubkov F.I.
The ring rearrangement metathesis (RRM) of a trans-cis diastereomer mixture of methyl 3-allyl-3a,6
The short route to chalcogenurea-substituted 3a,6-epoxyisoindoles via an intramolecular Diels-Alder furan (IMDAF) reaction. Antibacterial and antifungal activity
Mertsalov D.F., Shchevnikov D.M., Lovtsevich L.V., Novikov R.A., Khrustalev V.N., Grigoriev M.S., Romanycheva A.A., Shetnev A.A., Bychkova O.P., Trenin A.S., Zaytsev V.P.
Allyl amine
Application of the intramolecular Diels-Alder vinylarene (IMDAV) reaction for the synthesis of benzo-, carbocyclo-, thienothiopheneisoindolecarboxylic acids and its limitations
Yakovleva E.D., Shelukho E.R., Nadirova M.A., Erokhin P.P., Simakova D.N., Khrustalev V.N., Grigoriev M.S., Novikov A.P., Romanycheva A.A., Shetnev A.A., Bychkova O.P., Trenin A.S., Zubkov F.I., Zaytsev V.P.
Allyl amine
An intramolecular Diels–Alder reaction in the synthesis of N-aroyl-3a,6-epoxyisoindole-2-carbothioamides
Mertsalov D.F., Lovtsevich L.V., Shchevnikov D.M., Dobrushina Y.M., Sorokina E.A., Grigoriev M.S., Zaytsev V.P.
(Figure presented.) The reaction of allyl(furfuryl)amines with aroyl isothiocyanates was studied
Synthesis of 2-furilpergidroaza heterocycles and their transformation under the influence of anhydrides unsaturated's acids
Miteo Yvan
if the furan fragment is in the α-position. We synthesized cyclic α-furilsubstituted amines, and the example
Not all carbon—carbon bonds are equivalent: anomeric effect of sp-hybridized carbon atom
Vatsadze S.Z., Medved’ko A.V., Mirakbarov M.K., Minyaev M.E., Khrustalev V.N., Zaripov D.U., Medvedev M.G., Alabugin I.V.
, which can affect the reactivity of acetylenes. For the N-benzyl systems (9.4 kcal mol−1) and N-allyl (9
Imino [4+4] cycloaddition products as exclusive and biologically relevant acrolein-amine conjugates are intermediates of 3-formyl-3,4-dehydropiperidine (FDP), an acrolein biomarker
Takamatsu M., Fukase K., Kurbangalieva A., Tanaka K.
of the reaction, through an imino [4+4] cycloaddition, of biologically relevant amines with acrolein
Synthesis of epoxyisoindolo[1,2-a]isoquinolinium salts by an intramolecular [2+4] cycloaddition reaction in 2-allyl-1-furylisoquinolinium halides
Zubkov F.I., Zaytsev V.P., Obushak M.D., Ershova Y.D., Mertsalov D.F., Sorokina E.A., Nikitina E.V., Gorak Y.I., Lytvyn R.Z., Varlamov A.V.
by various allyl halides. It was found that the process occurred through the intermediate formation of 2

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