Краткие описания именных реакций .
Схема и ссылка на встреченные мною в современной литературе именные реакции.
Русские названия предлагаются по моему разумению в скобках.
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Схема и ссылка на встреченные мною в современной литературе именные реакции. Русские названия предлагаются по моему разумению в скобках. |
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Англ. Название |
Литература |
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Aza-Baylis-Hillman Reaction |
Shi, Y.-L.; Shi, M. , European J. of Org. Chem. 2007, (18), 2905-16. (Обзор) |
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Barbier-type allylation reaction |
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| Biginelli Pyrimidine Synthesis | |
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Blaser-Heck reaction (Blaser reaction) |
H.-U. Blaser, A. Spencer, J. Organomet. Chem. 1982, 233, 267. |
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Cacсhi reaction (Arcadi-Cacchi reaction) |
G. Balme, D. Bouyssi et al. Synthesis 2003, 2115-2134. (Обзор) |
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Claisen rearrangement, 102, 277 |
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Doering/Parikh conditions SO^-pyridine complex, 302 |
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Gennari-Evans-Vederas ("GEV") hydrazination, 12 |
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Clark zirconium allylation, 251 |
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Fischer glycosidation, 365 |
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Evans-Tishchenko reduction |
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Favorskii rearrangement, 443 |
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Grubbs-Hoveyda ring-closing metathesis reaction |
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Jones oxidation, 452 |
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Cope rearrangement, 387 |
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Corey-Brunelle macrolactonisation/method |
A. Parenty, X. Moreau, J.-M. Campagne, Chem. Rev. 2006, 106, 911-939. (Обзор) |
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Corey-Fuchs addition reaction, 214 |
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Corey-Nicolaou macrolactonisation/method |
A. Parenty, X. Moreau, J.-M. Campagne, Chem. Rev. 2006, 106, 911-939. (Обзор) |
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Darzens type reaction, 87 |
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Eschenmoser fragmentation, 73 |
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Finkelstein reaction, 289 |
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| Friedlander Quinoline Synthesis | Organic Reactions,Vol. 28 |
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Gerlach modification/macrolactonisation |
A. Parenty, X. Moreau, J.-M. Campagne, Chem. Rev. 2006, 106, 911-939. (Обзор) |
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Gif oxidation |
P. Stavropoulos, R. Çelenigil-Çetin, A. E. Tapper, Acc. Chem. Res. 2001, 34, 745–752. (Обзор) |
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Glaser coupling, 402, 407 |
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Glaser reaction |
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Halogen Dance Reaction |
Nora de Souza, M. V. Current Organic Chemistry 2007, 11(7), 637-46. (Обзор) M. Schnuerch, P. Stanetty et al. Chem. Soc. Rev., 2007, 36, 1046–1057. (Обзор) |
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Hofmann rearrangement, 302 |
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Johnson ortho-ester Claisen rearrangement, 260 |
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Johnson-Bartlett procedure, 54 |
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Julia coupling, 182 |
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Kinugasa Reaction. |
Pal, R.; Ghosh, S. C.; Chandra, K.; Basak, A., Synlett 2007, (15), 2321-30. (Обзор) |
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Krapcho decarbomethoxylation, 454 |
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Kunieda cleavage, 20 |
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Kunieda reaction, 21 |
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Lindgren oxidation, 484 |
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Lingrin oxidation, 432 |
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Luche conditions, 486 |
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Mannich reaction, 300, 302, 388 |
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Masamune reaction |
A. Parenty, X. Moreau, J.-M. Campagne, Chem. Rev. 2006, 106, 911-939. (Обзор) |
| Nef Reaction | Organic Reactions, Vol. 38 |
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Nicholas Reaction |
Diaz, D. D.; Betancort, J. M.; Martin, V. S. Synlett, 2007, (3), 343-59. (Обзор) |
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Hough-Richardson aziridine |
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Oppenauer oxidation |
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| Passerini reaction |
Doemling, A. Chemical Reviews 2006, 106(1), 17-89. (Обзор) L. Banfi, R. Riva, Organic Reactions, vol.65.. |
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Pauson-Khand reaction, 211, 212, 231, 232, 235, 236 |
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| Payne Rearrangement | |
| Petasis reaction |
Doemling, A. Chemical Reviews 2006, 106(1), 17-89. (Обзор) |
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Peterson elimination, 278 |
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Pictet-Spengler Reaction |
Organic Preparations and Procedures International 2006, 38(6), 505-91. (Обзор) |
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Pinner reaction, 329 |
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Prelog-Djerassi lactone, 173 |
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Prins Reaction.
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Pastor, I. M.; Yus, M. Current Organic Chemistry 2007, 11(10), 925-57. (Обзор) |
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Pudovik reaction |
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| Pummerer reaction | Organic Reactions, Vol. 40 |
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Garner-type oxidation, 8 |
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| Ramberg-Backlund reaction | Organic Reactions, Vol. 25 |
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Rebek's imide, 378 |
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The Rauhut-Currier Reaction |
10.1016/j.tet.2009.02.066 |
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Reformatsky Reaction |
Cozzi, P. G. Angewandte Chemie, Int. Ed. 2007, 46(15), 2568-71. (Обзор) |
| Reimer-Tiemann Reaction | Organic Reactions, Vol .28 |
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Rossi reaction |
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Schmidt or Beckmann rearrangement, 349 |
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Schotten-Baumann conditions, 18 |
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Schreiber ozonolysis, 15 |
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Sharpless-Kresze allylic amination, 360 |
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Shilov reaction |
A. E. Shilov, G.B. Shul’pin, Chem. Rev. 1997, 97, 2879–2932. (Обзор) |
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sila-Sonogashira reaction |
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Simmons-Smith reaction |
Organic Reactions Vol. 58 |
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Garner oxidation, 11 |
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Smiles rearangement |
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Staudinger reduction, |
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Steglich reaction/esterification |
A. Parenty, X. Moreau, J.-M. Campagne, Chem. Rev. 2006, 106, 911-939. (Обзор) |
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Stork-Wittig reaction, 124 |
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Strecker reaction, 324, 329 |
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Takai-Utimoto reagent, 173, 191-192, 208, 211 |
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Takeda reagent, 206 |
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Tennant quinoline synthesis, 7 |
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Tykwinski's triyne synthesis, 225 |
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| Ugi reaction |
Doemling, A. Chemical Reviews 2006, 106(1), 17-89. (Обзор) |
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Ullmann coupling, 163, 422, 424 |
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Ullmann reaction, 146 |
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Vasella reductive ring-cleavage, 369, 375 |
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| Vilsmeier reaction | Organic Reactions, Vol 49. |
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Wacker-Tsuji reaction |
T. Takahashi, K. Kasuga, J. Tsuji, Tetrahedron Lett. 1978, 4917. (b) J. Tsuji, Synthesis 1984, 369. (Обзор) |
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Witkop-Winterfeldt Oxidation of Indoles |
Mentel, M.; Breinbauer, R. Current Organic Chemistry, 2007, 11(2), 159-76. (Обзор) |
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Wolff-Kishner reaction, 53 |
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Yamaguchi-Yonemitsu protocol, 200 |
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Zhao olefination, 288, 289 |