Нуклеофильное раскрытие донорно-акцепторных циклопропанов азид-ионом в синтезе N-гетероциклов (1105641), страница 32
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– P. 138–147.136. Ravelli, D. Benzoyl radicals from (hetero)aromatic aldehydes. Decatungstate photocatalyzedsynthesis of substituted aromatic ketones / D. Ravelli, M. Zema, M. Mella, M. Fagnoni, A. Albini //Org. Biomol. Chem. – 2010. – V. 8. – № 18. – P. 4158–4164.137. Kato, T. An approach to the synthesis of fujenoic acid / T. Kato, T. Suzuki, N. Ototani, H. Maeda,K. Yamada, Y. Kitahara // J. Chem. Soc.
Perkin Trans. 1 – 1977. – № 2. – P. 206–210.138. McKennis, H. Metabolites of nicotine and a synthesis of nornicotine / H. McKennis, L. B.Turnbull, H. N. Wingfield, L. J. Dewey // J. Am. Chem. Soc. – 1958. – V. 80. – № 7. – P. 1634–1636.139. Vo-Thanh, G. Synthesis of 15N-labelled nornicotine and 15N-labelled nicotine / G. Vo-Thanh, F.X. Felpin, G. Nourrisson, M. Trierweiler, R. J.
Robins, J. Lebreton // J. Label. Compd. Radiopharm. –2001. – V. 44. – № 13. – P. 881–888.140. Dehnel, A. Α-Aminophosphonates. III. Cycloaddition anionique-1,3 des esters α,β-insaturés:préparation et transformations des Δ1-pyrrolines / A. Dehnel, J. M. Kanabus-Kaminska, G. Lavielle //Can. J. Chem. – 1988. – V. 66. – № 2. – P. 310–318.141. Petruso, S. Oxidative halogenation of substituted pyrroles with Cu(II). Part II. Bromination ofsome ethyl 3-pyrrolecarboxylates and corresponding acids / S.
Petruso, S. Caronna, M. Sferlazzo, V.Sprio // J. Heterocycl. Chem. – 1990. – V. 27. – № 5. – P. 1277–1280.142. Tsuge, O. A new general route to N-protonated azomethine ylides from N-(silylmethyl)amidinesand -thioamides. Cycloaddition of synthetic equivalents of nitrile ylides / O. Tsuge, S. Kanemasa, K.Matsuda // J. Org. Chem. – 1986. – V.
51. – № 11. – P. 1997–2004.143. Mataka, S. A novel ring transformation of 3a,5,6a-triaryl-3,3a-dihydro-2H-furo(3,2-b)pyrrole2,6(6aH)-diones into 3-aroyl-2,5-diarylpyrrole derivatives / S. Mataka, H. Suzuki, K. Uehara, M.Tashiro // Bull. Chem. Soc. Jpn. – 1992. – V. 65. – № 10. – P.
2611–2615.144. Lui, K. Synthesis and chemistry of azolenines. Part 16. Preparation of both 3H- and 2H-pyrrolesfrom 2,2-disubstituted 1,4-diketones via the Paal-Knorr reaction, and isolation of intermediate 2hydroxy-3,4-dihydro-2H-pyrroles / K. Lui, M. P. Sammes // J. Chem. Soc. Perkin Trans. 1 – 1990. –№ 3. – P. 457–468.174145. Terry, W. G. 809.
Pyrroles and related compounds. Part VII. A synthesis of pyrroles from estersof toluene-p-sulphonylglycine / W. G. Terry, A. H. Jackson, G. W. Kenner, G. Kornis // J. Chem. Soc.– 1965. – P. 4389–4393.146. Brown, D. Synthesis of N-substituted prodigiosenes / D. Brown, D. Griffiths, M. E. Rider, R. C.Smith // J. Chem. Soc. Perkin Trans. 1 – 1986. – P. 455–463.147. Bratton, L. D. Discovery of pyrrole-based hepatoselective ligands as potent inhibitors of HMGCoA reductase / L.
D. Bratton, B. Auerbach, C. Choi, L. Dillon, J. C. Hanselman, S. D. Larsen, G. Lu,K. Olsen, J. A. Pfefferkorn, A. Robertson, C. Sekerke, B. K. Trivedi, P. C. Unangst // Bioorg. Med.Chem. – 2007. – V. 15. – № 16. – P. 5576–5589.148. Chang, C. K. Phenylpyrroles by Suzuki cross coupling and a synthesis of type Itetramethyltetraphenylporphyrin / C.
K. Chang, N. Bag // J. Org. Chem. – 1995. – V. 60. – № 21. – P.7030–7032.149. Kim, M.-S. Synthetic intermediates, process for preparing pyrrolylheptanoic acid derivativestherefrom / M.-S. Kim, M.-H. Yoo, J.-K. Rhee, Y.-J. Kim, S.-J. Park, J.-H. Choi, S.-Y. Sung, H.-G.Lim, D.-W. Cha // Патент WO2009084827A2 рег. 09.07.2008 по заявке WO2008KR07350 от12.12.2008.150. Galliford, C. V. Pyrrolidinyl-spirooxindole natural products as inspirations for the development ofpotential therapeutic agents / C. V. Galliford, K. A.
Scheidt // Angew. Chem. Int. Ed. – 2007. – V. 46.– № 46. – P. 8748–8758.151. Lin, W. Reduction of azides to amines or amides with zinc and ammonium chloride as reductingagent / W. Lin, X. Zhang, Z. He, Y. Jin, L. Gong, A. Mi // Synth. Commun. – 2002. – V. 32. – № 21. –P. 3279–3284.152. Bella, M. Organocatalytic regio- and asymmetric C-Selective SNAr reactions–stereoselectivesynthesis of optically active spiro-pyrrolidone-3,3‘-oxoindoles / M.
Bella, S. Kobbelgaard, K. A.Jørgensen // J. Am. Chem. Soc. – 2005. – V. 127. – № 11. – P. 3670–3671.153. Campaña, A. G. Sodium tetramethoxyborate: an efficient catalyst for Michael additions ofstabilized carbon nucleophiles / A. G. Campaña, N. Fuentes, E. Gómez-Bengoa, C. Mateo, J. E. Oltra,A. M. Echavarren, J. M. Cuerva // J. Org. Chem. – 2007. – V. 72.
– № 21. – P. 8127–8130.154.Иванов,К.Л.Способполученияпроизводных5-(гетеро)арил-4,5,6,7-тетрагидротриазоло[1,5-a]пиридина / К. Л. Иванов, Е. В. Виллемсон, Е. М. Будынина, О. А.Иванова, И. В. Трушков // Патент РФ 2563254 рег. в Госреестре 21.08.2015 по заявке №2013131190 от 08.07.2013.175155. Akué-Gédu, R. Studies on pyrrolidinones. Synthesis of 4,5-fused-3-hydroxypyridinyl-2-propionicacid derivatives / R. Akué-Gédu, D. Couturier, J.-P. Hénichart, B.
Rigo, G. Sanz, L. Van Hijfte, A.Bourry // Tetrahedron – 2012. – V. 68. – № 4. – P. 1117–1127.156. Armarego, W. L. F.Purification of Laboratory Chemicals / W. L. F. Armarego, D. D. Perrin –Butterworth Heinemann, 1996. – Ed. 4 – 529 p.157. Беккер, Х. Органикум. В 2 т. / Х. Беккер, В.
Бергер – М.: Мир, 2008. – Т. 2. – 488 с.158. Berestovitskaya, V. M. 1,1-Bis(methoxycarbonyl)ethenes containing pyridine and benzimidazolefragments: synthesis and reactions with nitromethane / V. M. Berestovitskaya, E. S. Ostroglyadov, O.S. Vasil’yeva // Russ. J. Org.
Chem. – 2003. – V. 39. – № 2. – P. 282–283.159. O’Bannon, P. E. Catalytic cyclopropanation of alkenes with ethyl nitrodiazoacetate. A facilesynthesis of ethyl 1-nitrocyclopropanecarboxylates / P. E. O’Bannon, W. P. Dailey // J. Org. Chem. –1989. – V. 54.
– № 13. – P. 3096–3101.160. Johnson, C. R. S-Ethenylsulfoximine derivatives. Reagents for ethylenation of protic nucleophiles/ C. R. Johnson, J. P. Lockard, E. R. Kennedy // J. Org. Chem. – 1980. – V. 45. – № 2. – P. 264–271.161. Nilsson, B. M. Phenyl-substituted analogs of oxotremorine as muscarinic antagonists / B. M.Nilsson, H. M. Vargas, B.
Ringdahl, U. Hacksell // J. Med. Chem. – 1992. – V. 35. – № 2. – P. 285–294.162. Cheemala, M. N. New P,N-ferrocenyl ligands for the asymmetric Ir-catalyzed hydrogenation ofimines / M. N. Cheemala, P. Knochel // Org. Lett. – 2007. – V. 9. – № 16. – P. 3089–3092.163. Shu, C. Gold-catalyzed oxidative cyclization of chiral homopropargyl amides: synthesis ofenantioenriched γ-lactams / C. Shu, M.-Q. Liu, S.-S. Wang, L.
Li, L.-W. Ye // J. Org. Chem. – 2013. –V. 78. – № 7. – P. 3292–3299.164. McKennis, H. Demethylation of cotinine in vivo 1 / H. McKennis, L. B. Turnbull, E. R. Bowman,E. Wada // J. Am. Chem. Soc. – 1959. – V. 81. – № 15. – P. 3951–3954.165. Isomura, S. An immunotherapeutic program for the treatment of nicotine addiction: hapten designand synthesis / S.
Isomura, P. Wirsching, K. D. Janda // J. Org. Chem. – 2001. – V. 66. – № 12. – P.4115–4121.166. Welter, C. Enantioselective synthesis of (+)(R)- and (–)(S)-nicotine based on Ir-catalysed allylicamination / C. Welter, R. M. Moreno, S. Streiff, G. Helmchen // Org. Biomol. Chem. – 2005. – V. 3. –№ 18. – P. 3266–3268..