Pure and Applied Chemistry

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• Nowrouzi Farhad, Batey Robert A.: Regio- and Stereoselective Allylation and Crotylation of Indoles at C2 Through the Use of Potassium Organotrifluoroborate Salts. Angew. Chem. 2013, 125, 926. <http://dx.doi.org/10.1002/ange.201207978>
• Lichtenberg Crispin, Okuda Jun: Strukturell definierte Allylverbindungen der Hauptgruppenmetalle: Koordination und Reaktivität. Angew. Chem. 2013, 125, 5336. <http://dx.doi.org/10.1002/ange.201208942>
• Nowrouzi Farhad, Batey Robert A.: Regio- and Stereoselective Allylation and Crotylation of Indoles at C2 Through the Use of Potassium Organotrifluoroborate Salts. Angew. Chem. Int. Ed. 2013, 52, 892. <http://dx.doi.org/10.1002/anie.201207978>
• Lichtenberg Crispin, Okuda Jun: Structurally Defined Allyl Compounds of Main Group Metals: Coordination and Reactivity. Angew. Chem. Int. Ed. 2013, 52, 5228. <http://dx.doi.org/10.1002/anie.201208942>
• Lebed Ekaterina G., Belov Alexander S., Dolganov Alexander V., Vologzhanina Anna V., Novikov Valentin V., Kuznetsov Evgenii V., Voloshin Yan Z.: Template synthesis, structure and properties of 4-pyridinylboron-capped iron(II) clathrochelate precursors for Bubnov diallylation reaction. Inorganic Chemistry Communications 2013, 33, 57. <http://dx.doi.org/10.1016/j.inoche.2013.04.021>
• Lichtenberg Crispin, Spaniol Thomas P., Okuda Jun: Bis(allyl)gallium Cation, Tris(allyl)gallium, and Tetrakis(allyl)gallate: Synthesis, Characterization, and Reactivity. Inrog Chem 2012, 51, 2254. <http://dx.doi.org/10.1021/ic202293t>
• Oshima Kazuyuki, Ohmura Toshimichi, Suginome Michinori: Dearomatizing conversion of pyrazines to 1,4-dihydropyrazine derivatives via transition-metal-free diboration, silaboration, and hydroboration. Chem. Commun. 2012, 48, 8571. <http://dx.doi.org/10.1039/c2cc34086k>
• Jochmann Phillip, Leich Valeri, Spaniol Thomas P., Okuda Jun: Calcium-Mediated Dearomatization, CH Bond Activation, and Allylation of Alkylated and Benzannulated Pyridine Derivatives. Chem. Eur. J. 2011, 17, 12115. <http://dx.doi.org/10.1002/chem.201101489>
• Lichtenberg Crispin, Spaniol Thomas P., Okuda Jun: Reactivity of Tris(allyl)aluminum toward Pyridine: Coordination versus Carbometalation. Organomettalics 2011, 30, 4409. <http://dx.doi.org/10.1021/om200492f>
• BUBNOV YU. N.: ChemInform Abstract: Reductive Mono- and Trans-α,α′-diallylation of Aromatic Nitrogen Heterocycles by Allylboranes. ChemInform 2010, 25, no. <http://dx.doi.org/10.1002/chin.199432287>
• Gurskii M.E., Bubnov Yu.N., Erdyakov S.Yu., Kizas O.A., Kolomnikova G.D., Kuznetsov N.Yu., Potapova T.V., Varzatskii O.A., Voloshin Y.Z.: Allylic boranes are chemist’s best friends: Reactivity, applications, new opportunities. J Organomet Chem 2009, 694, 1754. <http://dx.doi.org/10.1016/j.jorganchem.2008.12.050>
• Zhun I. V., Ignatenko A. V.: Use of allylic boranes in organic syntheses. Synthesis of an analog of the alkaloid flustrabromine. Russ Chem Bull 2004, 53, 2221. <http://dx.doi.org/10.1007/s11172-005-0103-0>
• Pastukhov Fedor V, Yampolsky Ilia V, Bubnov Yuri N: Allylboration of functionalized isoquinolines. J Organomet Chem 2002, 657, 123. <http://dx.doi.org/10.1016/S0022-328X(02)01406-7>
• Bubnov Yu. N., Klimkina E. V.: Synthesis of some alkaloids using the allyl derivatives of boron (review). Chem Heterocycl Compd 1999, 35, 888. <http://dx.doi.org/10.1007/BF02252156>
• Bubnov Yu. N., Klimkina E. V., Lavrinovich L. I., Zykov A. Yu., Ignatenko A. V.: Reductive allylation of pyrrole with allylboranes. Synthesis oftrans- andcis-2,5-disubstituted pyrrolidines. Russ Chem Bull 1999, 48, 1696. <http://dx.doi.org/10.1007/BF02494816>
• Bubnov Yu. N., Demina E. E., Bel'sky V. K., Zatonsky G. V., Ignatenko A. V.: Stereoselective reductive tetraallylation of pyridinecarboxylic acids with triallylborane. Russ Chem Bull 1998, 47, 2249. <http://dx.doi.org/10.1007/BF02494291>
• Bubnov Yu. N., Klimkina E. V., Ignatenko A. V.: Preparation oftrans- andcis-2-allyl-6-alkyl(aryl)-1,2,3,6-tetrahydropyridines based on the reductivetrans-2,6-dialkylation of pyridine. Synthesis of (±)-epidihydropinidine and (±)-dihydropinidine. Russ Chem Bull 1998, 47, 451. <http://dx.doi.org/10.1007/BF02495652>
• Bubnov Yu. N., Klimkina E. V., Ignatenko A. V.: Stereoselective synthesis of (±)-indolizidines 167B and 209D and theirtrans-isomers based on the reductive allylboration of pyridine. Russ Chem Bull 1998, 47, 941. <http://dx.doi.org/10.1007/BF02498166>
• Bubnov Yu. N., Klimkina E. V., Ignatenko A. V.: Reductivetrans-1,3-dialkylation of isoquinoline on treatment with RLi and triallylborane. Russ Chem Bull 1998, 47, 1175. <http://dx.doi.org/10.1007/BF02503493>
• Bubnov Yu. N., Demina E. E., Ignatenko A. V.: Transformations of pyridine and deuteropyridine under the action of trimethallylborane and alcohols. Synthesis oftrans- andcis-2,6-dimethallyl-1,2,3,6-tetrahydropyridines and theirN-derivatives. Russ Chem Bull 1997, 46, 1306. <http://dx.doi.org/10.1007/BF02495933>
• Bubnov Yu. N., Pastukhov F. V., Ignatenko A. V.: Allylzinc bromide: reductivetrans-1,3-diallylation of isoquinoline and intramolecular cyclization of 2,4-dizinc derivative. Russ Chem Bull 1997, 46, 1975. <http://dx.doi.org/10.1007/BF02503803>
• Bubnov Yuri N., Klimkina Elena V., Ignatenko Anatoly V., Gridnev Ilya D.: trans-cis-Isomerization of trans-2-allyl-6-alkyl(aryl)-1,2,3,6-tetrahydropyridines on heating with triallylborane. Synthesis of (±)-dihydropinidine. Tetrahetron Lett 1997, 38, 4631. <http://dx.doi.org/10.1016/S0040-4039(97)00953-2>
• Bubnov Yuri N, Klimkina Elena V, Ignatenko Anatoly V, Gridnev Ilya D: Preparation of trans-2-allyl-6-alkyl(aryl)-1,2,3,6-tetrahydropyridines by reductive trans-2,6-dialkylation of pyridine. Synthesis of (±)-epidihydropinidine. Tetrahetron Lett 1996, 37, 1317. <http://dx.doi.org/10.1016/0040-4039(95)02383-6>
• Katritzky Alan R., Rachwal Stanislaw, Rachwal Bogumila: Recent progress in the synthesis of 1,2,3,4,-tetrahydroquinolines. Tetrahedron 1996, 52, 15031. <http://dx.doi.org/10.1016/S0040-4020(96)00911-8>
• Bubnov Yu. N.: Allylboranes: reductive mono andtrans-diallylation of aromatic nitrogen-containing heterocyclic compounds. Russ Chem Bull 1995, 44, 1156. <http://dx.doi.org/10.1007/BF00700882>