Collect. Czech. Chem. Commun.
1948, 13, 300-315
https://doi.org/10.1135/cccc19480300
L'acétylacétate γ-chlorocrotylé et sa cyclisation par l'acide sulfurique
O. Wichterle, J. Procházka and J. Hofman
Crossref Cited-by Linking
- Lin Zhaowei, Lu Maojian, Liu Boyi, Gao Jing, Huang Mingqiang, Gan Zhenhong, Cai Shunyou: Oxidative alkylation of alkenes with carbonyl compounds through concomitant 1,2-aryl migration by photoredox catalysis. New J. Chem. 2020, 44, 16031. <https://doi.org/10.1039/D0NJ03733H>
- Hagihara Shuichi, Hanaya Kengo, Sugai Takeshi, Shoji Mitsuru: Syntheses of Englerin A, a Potent Renal Cancer Inhibitor. Asian J Org Chem 2019, 8, 48. <https://doi.org/10.1002/ajoc.201800609>
- Chu Xue‐Qiang, Meng Hua, Zi You, Xu Xiao‐Ping, Ji Shun‐Jun: Metal‐Free Oxidative Radical Addition of Carbonyl Compounds to α,α‐Diaryl Allylic Alcohols: Synthesis of Highly Functionalized Ketones. Chemistry A European J 2014, 20, 17198. <https://doi.org/10.1002/chem.201404463>
- Rao H. Surya Prakash, Rao A. Veerabhadra, Desai Avinash: Domino Products from Select Mannich Salts and β-Keto Esters/β-Keto Nitriles. Proc. Natl. Acad. Sci., India, Sect. A Phys. Sci. 2013, 83, 195. <https://doi.org/10.1007/s40010-013-0076-6>
- Gao Peng, Cook Silas P.: A Reductive-Heck Approach to the Hydroazulene Ring System: A Formal Synthesis of the Englerins. Org. Lett. 2012, 14, 3340. <https://doi.org/10.1021/ol3013167>
- Yadav J. S., Antony Aneesh, George Jimil, Subba Reddy Basi V.: Recent Developments in Indium Metal and Its Salts in Organic Synthesis. Eur J Org Chem 2010, 2010, 591. <https://doi.org/10.1002/ejoc.200900895>
- Chapelon Anne-Sophie, Moraléda Delphine, Rodriguez Raphaël, Ollivier Cyril, Santelli Maurice: Enantioselective synthesis of steroids. Tetrahedron 2007, 63, 11511. <https://doi.org/10.1016/j.tet.2007.08.087>
- Konstantinova Olga, Sarabèr Florence C.E., Melguizo Enrique, Jansen Ben J.M., de Groot Aede: 1-Phenylthio-3-vinyl-3-cyclohexenol, a new reagent for bis-annelation of silyl enol ethers. Tetrahedron 2006, 62, 1749. <https://doi.org/10.1016/j.tet.2005.11.060>
- Claramunt Rosa M., López Concepción, Pérez-Medina Carlos, Pinilla Elena, Torres M. Rosario, Elguero José: Synthesis and structural study of tetrahydroindazolones. Tetrahedron 2006, 62, 11704. <https://doi.org/10.1016/j.tet.2006.09.043>
- van der Steen R., Biesheuvel P. L., Lugtenburg J., Erkelens C., Mathies R. A.: 8,16‐ And 8,18‐methanobacteriorhodopsin. Synthesis and spectroscopy of 8,16‐ and 8,18‐methanoretinal and their interaction with bacterioopsin. Recl. Trav. Chim. Pays‐Bas 1989, 108, 83. <https://doi.org/10.1002/recl.19891080302>
- Bhattacharya Apurba, Dolling Ulf‐H., Grabowski Edward J. J., Karady Sandor, Ryan Kenneth M., Weinstock Leonard M.: Enantioselektive Robinson‐Anellierung unter Phasentransfer‐Katalyse. Angewandte Chemie 1986, 98, 442. <https://doi.org/10.1002/ange.19860980507>
- Bhattacharya Apurba, Dolling Ulf‐H., Grabowski Edward J. J., Karady Sandor, Ryan Kenneth M., Weinstock Leonard M.: Enantioselective Robinson Annelations via Phase‐Transfer Catalysis. Angew. Chem. Int. Ed. Engl. 1986, 25, 476. <https://doi.org/10.1002/anie.198604761>
- Duhamel P., Hennequin L., Poirier J.M., Tavel G., Vottero C.: 1,5-Dicarbonyl compounds. Tetrahedron 1986, 42, 4777. <https://doi.org/10.1016/S0040-4020(01)82058-5>
- Duhamel Pierre, Poirier Jean-Marie, Tavel Gilbert: Nouvelle Méthode d'annelation par l'intermédiaire de dicétones-1,5. Tetrahedron Letters 1984, 25, 43. <https://doi.org/10.1016/S0040-4039(01)91143-8>
- Conrow Raymond E., Marshall James A.: Improved Preparation of Methyl 3-Chloro-2-Butenoate; Precursor of the Wichterle Annulation Reagent, 1,3-Dichloro-2-Butene. Synthetic Communications 1981, 11, 419. <https://doi.org/10.1080/00397918108064310>
- Fráter György: Über die Stereoselektivität der α‐Alkylierung von (1R, 2S) (+)‐cis‐2‐hydroxy‐cyclohexancarbonsäureäthylester. Helvetica Chimica Acta 1980, 63, 1383. <https://doi.org/10.1002/hlca.19800630605>
- Kobayashi Makoto, Matsumoto Takeshi: Modifizierte Wichterle-Reaktion. Ein Weg zur Darstellung von 2-Cyclohexenonen und 1,4-Diketonen. Synthese von 4-Estren-3,17-dion und Dihydrojasmon. Bulletin of the Chemical Society of Japan 1979, 52, 2978. <https://doi.org/10.1246/bcsj.52.2978>
- Jung Michael E.: A review of annulation. Tetrahedron 1976, 32, 3. <https://doi.org/10.1016/0040-4020(76)80016-6>
- Kobayashi Makoto, Matsumoto Takeshi: MODIPIZIERTE WICHTERLE REAKTION. EIN NEUER WEG ZUR SYNTHESE VON Δ2-CYCLOHEXENONEN. Chemistry Letters 1973, 2, 957. <https://doi.org/10.1246/cl.1973.957>
- Muntyan G. E., Smit V. A., Semenovskii A. V., Kucherov V. F.: Synthesis of 2-methyl-1-hepten-6-one (?-methylheptenone) and some other terpenes of the?-series. Russ Chem Bull 1972, 21, 861. <https://doi.org/10.1007/BF00854488>
- Lawesson Sven‐Olov, Larsen Erik Holger, Jakobsen Hans Jørgen, Frisell Christer: Studies on elimination VII. Syntheses of D,L‐Piperitone (D,L‐Δ1‐p‐Menthen‐3‐one) and Related Compounds from t‐butyl β‐keto‐esters. Recl. Trav. Chim. Pays‐Bas 1964, 83, 464. <https://doi.org/10.1002/recl.19640830505>
- Adam Günter: Wege zur Totalsynthese pflanzlicher Steroide Teil I. Zeitschrift fuer Chemie 1963, 3, 379. <https://doi.org/10.1002/zfch.19630031004>
- Velluz L., Nominé G., Mathieu J.: Neuere Ergebnisse bei der Totalsynthese von Steroiden. Angewandte Chemie 1960, 72, 725. <https://doi.org/10.1002/ange.19600721903>
- Prelog V., Barman P., Zimmermann M.: Zur Kenntnis des Kohlenstoffringes. 51. Mitteilung. Weitere Untersuchungen über die Gültigkeitsgrenzen der Bredt'schen Regel. Eine Variante der Robinson'schen Synthese von cyclischen ungesättigten Ketonen. Helvetica Chimica Acta 1949, 32, 1284. <https://doi.org/10.1002/hlca.19490320418>