Manuel Jiménez
National Autonomous University of Mexico
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Featured researches published by Manuel Jiménez.
Tetrahedron | 1977
Lydia Rodríguez-Hahn; Manuel Jiménez; Eduardo Díaz; Carlos A. Guerrero; Alfredo Ortega; A.Romo de Vivar
Abstract The structure 1 previously proposed tor mortonin, is revised to 2 based on spectroscopic and chemical evidence, and on biogenetic considerations.
Phytochemistry | 1982
Mariano Martínez; A. Romo de Vivar; Eduardo Díaz; Manuel Jiménez; Lydia Rodríguez-Hahn
Abstract The structure of mortonol B, a sesquiterpene constituent of Mortonia hidalgensis , was established as 2β-acetoxy-mortonol A. Mortonol B is propose
Phytochemistry | 1981
Lydia Rodríguez-Hahn; M. Mora; Manuel Jiménez; R. Saucedo; Eduardo Díaz
Abstract The structure of mortonol A isolated from Mortonia greggii was established as a benzoate diester of 1α,4β,9β-trihydroxy-dihydroagarofurane-6-one. Its structure and stereochemistry were determined by chemical and spectroscopic means.
Phytochemistry | 1988
Manuel Jiménez; Edgar Tovar García; Leticia Gardida; Alfonso Lira-Rocha
Abstract The structures of Rzedowskins A, B, C and D, new sesquiterpenes of the polyhydroxyagarofuran-type and constituents of Rzedowskia tolantonguensis, were established by chemical and spectroscopic methods.
Phytochemistry | 1978
Alfonso Romo de Vivar; Ana L. Pérez; Héctor Daniel Hernández Flores; Lydia Rodríguez-Hahn; Manuel Jiménez
Abstract Four sesquiterpene lactones were isolated from several populations of Parthenium confertum var. lyratum (Gray) collected in Sierra de Arteaga, southern Coahuila. Three of the compounds, hysterin, tetraneurin E and hymenin were previously isolated from other Parthenium species. The fourth constituent is the new cyclopropanoid sesquiterpene dilactone confertdiolide which represents a new structural type. The photolytic conversion of hymenin into confertdiolide confirmed its structure.
Tetrahedron | 1977
Lydia Rodríguez-Hahn; Manuel Jiménez; Eduardo Díaz; Carlos A. Guerrero; Alfredo Ortega; A. Romo de Vivar
Abstract Irradiation of mortonin (2a), gave an isomeric photoproduct called photomortonin, whose structure was proved to be 3a.
Tetrahedron | 1983
Lydia Rodríguez-Hahn; Manuel Jiménez; R. Saucedo; Manuel Soriano-García; Rubén A. Toscano; Eduardo Díaz
Abstract The photolysis of tetrahydro zexbrevin 2, gave in high yield the photoisomerization product 3, its structure was determined by chemical and spectroscopic means. The formation of the photoproduct 3 could involve an intramolecular hydrogen shift. The photoproducts 7 and 9 were also isolated and their structures determined.
Journal of Natural Products | 1987
Alfonso Lira-Rocha; Raul Diaz; Manuel Jiménez
Pesticide Science | 1994
José Luis Mendoza; Manuel Jiménez; Blas Lotina-Hennsen
Revista Iberoamericana de Educación | 2011
Jorge Barojas-Weber; Raymundo David López López; Manuel Jiménez