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AtanasP. Venkov & Stela Statkova-Abeghe. (1998) α-Amidoalkylation Reactions and Oxidation of Adducts of Benzimidazoles and Acyl Chlorides. Synthetic Communications 28:10, pages 1857-1864.
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AtanasP. Venkov & Stela Statkova-Abeghe. (1996) Synthesis of 1-(2-Oxoalkyl)-2-acyltetrahydro-isoquinolines by α-Amidoalkylation of Methylene Active Carbonyl Compounds with N-Acyliminium Intermediates. Synthetic Communications 26:11, pages 2135-2144.
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AtanasP. Venkov & Stela Statkova-Abeghe. (1996) Synthesis of 1-Aryl-2-acyltetrahydroisoquinolines with an Electron Withdrawing Group in the Aromatic Ring of Heterocycle. Synthetic Communications 26:1, pages 127-134.
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AtanasP. Venkov & StelaM. Statkova-Abeghe. (1995) Application of the Intermolecular α-Amido-alkylation Reaction for the Synthesis of Tertiary Amides and 1-Substituted 2-Acyltetrahydroiso-Quinolines. Synthesis of (±)-Carnegine. Synthetic Communications 25:12, pages 1817-1824.
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Articles from other publishers (5)
Erwan Le Gall, Antoine Pignon & Thierry Martens. (2011) A practical route to tertiary diarylmethylamides or -carbamates from imines, organozinc reagents and acyl chlorides or chloroformates. Beilstein Journal of Organic Chemistry 7, pages 997-1002.
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George A. Olah, G. K. Surya Prakash, Qi Wang, Xing-ya Li & Thomas Ziegler. 2001. Encyclopedia of Reagents for Organic Synthesis. Encyclopedia of Reagents for Organic Synthesis.
Atanas Venkov, Stela Statkova-Abeghe & Atanaska Donova. (2004) Amidoalkylation of heteroaromatic compounds with adducts of acyl chlorides and 3,4-dihydroisoquinoline and isoquinoline. Open Chemistry 2:1, pages 234-246.
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Atanas P. Venkov & Stela M. Statkova-Abeghe. (1996) Synthesis of 3,4-dihydroisoquinolines, 2-alkyl(Acyl)-1(2H)-3,4-dihydroisoquinolinones, 2-alkyl-1(2H)-isoquinolinones and 1-alkyl-2(2H)-quinolinones by oxidation with potassium permanganate. Tetrahedron 52:4, pages 1451-1460.
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A. P. VENKOV, S. M. STATKOVA & I. I. IVANOV. (2010) ChemInform Abstract: Synthesis of 1‐Phenyl‐2‐acyltetrahydroisoquinolines by Intermolecular . alpha.‐Amidoalkylation Reaction.. ChemInform 23:23.
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