Collection of Czechoslovak Chemical Communications - digital archive 

Crossref Cited-by Linking

• Lou Guanhua, Huang Yan, Wang Yu, Chen Shiyun, Liu Chang, Li Ying, Feng Jianan: Germacrone, A Novel and Safe Anticancer Agent from Genus Curcuma: A Review of its Mechanism. ACAMC 2023, 23, 1490. <https://doi.org/10.2174/1871520623666230420094628>
• Xu Houchao, Dickschat Jeroen S: Germacrene B – a central intermediate in sesquiterpene biosynthesis. Beilstein J. Org. Chem. 2023, 19, 186. <https://doi.org/10.3762/bjoc.19.18>
• Srivilai Jukkarin, Khorana Nantaka, Waranuch Neti, Wisuitiprot Wudtichai, Suphrom Nungruthai, Suksamrarn Apichart, Ingkaninan Kornkanok: Germacrene Analogs are Anti-androgenic on Androgen-dependent Cells. Natural Product Communications 2016, 11, 1934578X1601100. <https://doi.org/10.1177/1934578X1601100906>
• Adio Adewale M.: Germacrenes A–E and related compounds: thermal, photochemical and acid induced transannular cyclizations. Tetrahedron 2009, 65, 1533. <https://doi.org/10.1016/j.tet.2008.11.050>
• Barrero Alejandro F., Herrador M. Mar, Arteaga Pilar, Catalán Julieta V.: Germacrone: Occurrence, Synthesis, Chemical Transformations and Biological Properties. Natural Product Communications 2008, 3, 1934578X0800300. <https://doi.org/10.1177/1934578X0800300418>
• Hooper A. M., Farcet J.-B., Mulholland N. P., Pickett J. A.: Synthesis of 9-methylgermacrene B, racemate of the sex pheromone of Lutzomyia longipalpis (Lapinha), from the renewable resource, Geranium macrorrhizum essential oil. Green Chem. 2006, 8, 513. <https://doi.org/10.1039/b602875f>
• Hanuš Lumír O., Řezanka Tomáš, Dembitsky Valery M., Moussaieff Arieh: Myrrh - Commiphora chemistry. Biomed Pap Med Fac Univ Palacky Olomouc Czech Repub 2005, 149, 3. <https://doi.org/10.5507/bp.2005.001>
• Piet Dennis P., Schrijvers Robert, Franssen Maurice C.R., de Groot Aede: Biotransformation of germacrane epoxides by Cichorium intybus. Tetrahedron 1995, 51, 6303. <https://doi.org/10.1016/0040-4020(95)00272-A>
• Enev Valentin, Tsankova Elena: Biomimetic germacrene-humulene rearrangement. Tetrahedron Letters 1988, 29, 1829. <https://doi.org/10.1016/S0040-4039(00)82056-0>
• Jacobsson Ulla, Norin Torbjörn, Weber Michael, Tsankova Elena: The configuration and conformation of isogermacrone. The significance of crossed conformations in olefinic cyclisations. Tetrahedron 1985, 41, 2033. <https://doi.org/10.1016/S0040-4020(01)96572-X>
• Simova S. D., Bozhkova N. V., Orahovats A. S.: 1H and 13C NMR studies of some germacrones and isogermacrones. Org. Magn. Reson. 1984, 22, 431. <https://doi.org/10.1002/mrc.1270220707>
• Fransen Harrie R., Dormans Guido J.M., Buck Henk M.: Conformational dependent regio- and stereo-selectivity in transformations of germacrenes. Tetrahedron 1983, 39, 2981. <https://doi.org/10.1016/S0040-4020(01)92160-X>
• Tsankova E., Ognyanov I., Norin T.: Transannular cyclisation of germacrone and isogermacrone via oxymercuration-demercuration. Tetrahedron 1980, 36, 669. <https://doi.org/10.1016/0040-4020(80)88012-4>
• Marshall James A.: Trans-cycloalkenes and [a.b]betweenanenes, molecular jump ropes and double bond sandwiches. Acc. Chem. Res. 1980, 13, 213. <https://doi.org/10.1021/ar50151a004>
• Talman E., Verwiel P. E. J., Ritter F. J., Persoons C. J.: Sex Pheromones of the American Cockroach, Periplaneta americana. Israel Journal of Chemistry 1978, 17, 227. <https://doi.org/10.1002/ijch.197800040>
• Hill Richard K., Fracheboud Michel G., Sawada Seiji, Carlson Robert M., Yan Shou-Jen: Partial resolution of germacrone. An optically active dissymmetric trans, trans-1,5-cyclodecadiene. Tetrahedron Letters 1978, 19, 945. <https://doi.org/10.1016/S0040-4039(01)85421-6>
• Tsankova E., Ognyanov I.: Germazone, a novel tricyclic sesquiterpene ketone in the essential oil from geranium macrorrhizum L. Tetrahedron Letters 1976, 17, 3833. <https://doi.org/10.1016/S0040-4039(00)93123-X>
• Yeh Ping–Hsien: Essential Oils XVII. Oil of Pogostemon Formosanus Oliv. II Isolation and Chemistry of Germacrone. J Chinese Chemical Soc 1975, 22, 237. <https://doi.org/10.1002/jccs.197500028>
• Sutherland J.K.: Regio- and stereo-specificity in the cyclisation of medium ring 1,5-dienes. Tetrahedron 1974, 30, 1651. <https://doi.org/10.1016/S0040-4020(01)90687-8>
• Rüiker Gerhard: Sesquiterpene. Angewandte Chemie 1973, 85, 895. <https://doi.org/10.1002/ange.19730852003>
• Rücker Gerhard: Sesquiterpenes. Angew. Chem. Int. Ed. Engl. 1973, 12, 793. <https://doi.org/10.1002/anie.197307931>
• Nakashima Ruka, Yoshikawa Masaharu, Matsuura Teruo: Quercetin 3,7,3′,4′-tetramethyl ether from Germanium macrorhizum. Phytochemistry 1973, 12, 1502. <https://doi.org/10.1016/0031-9422(73)80600-4>
• Ganter C., Keller‐Wojtkiewicz Frau B.: Pyrolysen‐ und Hydrierungsversuche in der Elemol‐ und Dihydrogeijeren‐Reihe. Helvetica Chimica Acta 1971, 54, 183. <https://doi.org/10.1002/hlca.19710540117>
• Morikawa K., Hirose Y.: Germacrene-c, precursor of δ-elemene. Tetrahedron Letters 1969, 10, 1799. <https://doi.org/10.1016/S0040-4039(01)88015-1>
• Šorm F.: Sesquiterpenoide mit zehngliedrigem Ring. Angewandte Chemie 1967, 79, 64. <https://doi.org/10.1002/ange.19670790128>
• Šorm F.: Sesquiterpenoids with Ten‐Membered Rings. Angew. Chem. Int. Ed. Engl. 1967, 6, 94. <https://doi.org/10.1002/anie.196700942>
• Joshi B.N., Chakravarti K.K., Bhattacharyya S.C.: Terpenoids—XCVII. Tetrahedron 1967, 23, 1251. <https://doi.org/10.1016/0040-4020(67)85075-0>
• Mathur S.B., Kulkarni G.H., Kelkar G.R., Bhattacharyya S.C.: Terpenoids—LVII. Tetrahedron 1964, 20, 2903. <https://doi.org/10.1016/S0040-4020(01)98511-4>
• Ohloff G.: Zur Pyrolyse des Germacrons. Angew. Chem. 1959, 71, 162. <https://doi.org/10.1002/ange.19590710413>
• Ohloff Günther, Farnow Heinz, Philipp Wolfgang, Schade Gerhard: Über Germacron und seine pyrolytische Umwandlung. Justus Liebigs Ann. Chem. 1959, 625, 206. <https://doi.org/10.1002/jlac.19596250127>
• Hendrickson J.B.: Stereochemical implications in sesquiterpene biogenesis. Tetrahedron 1959, 7, 82. <https://doi.org/10.1016/0040-4020(59)80055-7>