Zobrazeno 1 - 10
of 13
pro vyhledávání: '"Pedro I. Ramirez-Montes"'
Autor:
H. V. Rasika Dias, Pedro I. Ramirez-Montes, Jesús A. Lara-Cerón, Víctor M. Jiménez-Pérez, Areli A. Molina-Paredes, Blanca M. Muñoz-Flores, Mario Sánchez
Publikováno v:
New Journal of Chemistry. 45:1727-1733
In the present work, we report the green synthesis of a Shiff base [N-(2-hydroxy-1-naphthylidene)-L-phenylalanine (1)] derived from an α-amino acid through an ultrasound-assisted synthesis method with excellent chemical yield in a short period of ti
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::bb743732bef76aa9700b301054c7a80f
https://doi.org/10.1039/d0nj04720a
https://doi.org/10.1039/d0nj04720a
Autor:
Marco A. Leyva, Norberto Farfán, Herbert Höpfl, Pedro I. Ramirez-Montes, Rafael Arcos-Ramos, María E. Ochoa, Rosa Santillan
Publikováno v:
Crystal Growth & Design. 19:6114-6126
The synthesis, characterization, and crystal structure analysis of five new steroidal molecular rotors constructed from two different building blocks, viz., mestranol, ethynylestradiol, levonorgest...
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::b7fc9ac75d61903a5ac50663a70754fd
https://doi.org/10.1021/acs.cgd.9b00238
https://doi.org/10.1021/acs.cgd.9b00238
Autor:
Eduardo Arias, Blanca M. Muñoz-Flores, Gleb Turlakov, Casiano Del Angel-Mosqueda, Arelly M. Cantón-Díaz, Ivana Moggio, Víctor M. Jiménez-Pérez, Pedro I. Ramirez-Montes
Publikováno v:
Journal of Molecular Structure. 1180:642-650
A couple of luminescent organotin compounds derivated from ligands-ONO were obtained by multicomponent microwave assisted synthesis in short time (15 min) and good yields: ((E)-8, 8-8-diphenylbenzo[d] naphtho [1,2-h][1,3,6,2] dioxazastannonine (1) an
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::e1de9cdf3d9d13c521e72a8bbb08e509
https://doi.org/10.1016/j.molstruc.2018.12.039
https://doi.org/10.1016/j.molstruc.2018.12.039
Autor:
Yliana López, Norberto Farfán, María E. Ochoa, Andrés Aguilar-Granda, Rosa Santillan, Pedro I. Ramirez-Montes, Victor Barba
Publikováno v:
CrystEngComm. 18:6830-6840
Thirteen steroidal derivatives were synthesized through a Sonogashira cross-coupling reaction which has been found to be an excellent synthetic strategy to introduce halo-aromatic groups into C-17-ethynyl substituted steroidal frameworks. The structu
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::474bf617d764c462fc8d87c69125f04b
https://doi.org/10.1039/c6ce01056c
https://doi.org/10.1039/c6ce01056c
Autor:
Jorge O. Virues, Pedro I. Ramirez-Montes, José María Rivera, Jesús A. Arenzano, Jorge M. del Campo, Rosa Santillan
Publikováno v:
Journal of Molecular Structure. 1083:106-110
The solvothermal reaction of Co(NO3)2⋅6H2O, Pyrazine (L1) and 5-Aminoisophthalic acid (L2) let to the formation of a new functionalized pillared coordination polymer with possible application as a carrier system for drug delivery. The X-ray diffrac
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::104b80bdc887fcce6f78a699fe37dc04
https://doi.org/10.1016/j.molstruc.2014.11.042
https://doi.org/10.1016/j.molstruc.2014.11.042
Autor:
Jorge O. Virues, Raúl Colorado-Peralta, Jesús A. Arenzano, Pedro I. Ramirez-Montes, José María Rivera, Rosa Santillan, Mario Sánchez
Publikováno v:
Inorganic Chemistry Communications. 51:55-60
Coordination cobalt and nickel complexes (1) and (2) were obtained serendipitously by the reaction of M(NO3)2·6H2O (M = Co and Ni) and methyliminodiacetic acid (H2L) in a mixture of solvents. The X-ray diffraction showed the unusual structures with
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::e28e2193b19e98f515945909b0d1faee
https://doi.org/10.1016/j.inoche.2014.10.037
https://doi.org/10.1016/j.inoche.2014.10.037
Autor:
Norberto Farfán, Edgar Gonzalez-Rodriguez, Rosa Santillan, Pedro I. Ramirez-Montes, María E. Ochoa, Rafael Arcos-Ramos, Miguel A. Garcia-Garibay, Braulio Rodríguez-Molina
Publikováno v:
RSC Advances. 5:55201-55208
In this work, we describe the synthesis and solid-state characterization of a series of molecular rotors with tri-isopropylsilyloxy-substituted (TIPS) trityl stators axially linked to 1,4-diethynylphenylene, 3,6-diethynyl-1,2-difluorophenylene and 2,
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::ce138b99febb257f77d705ba89884858
https://doi.org/10.1039/c5ra07422c
https://doi.org/10.1039/c5ra07422c
Publikováno v:
Crystal Growth & Design. 14:4681-4690
The synthesis and crystal structure of three new molecular rotors derived from levonorgestrel and norethisterone are reported. The conformation, close contacts, and shape characteristics of these molecules exhibiting Z′ = 2 and the inclusion of sol
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::a11ff8725bcc6044ca69586f4673020b
https://doi.org/10.1021/cg500772f
https://doi.org/10.1021/cg500772f
Autor:
Patricia Rodríguez, Pedro I. Ramirez-Montes, María E. Ochoa, Norberto Farfán, Rosa Santillan, Vianey Rodríguez, Héctor García-Ortega
Publikováno v:
Tetrahedron Letters. 53:5887-5890
The synthesis and structural characterization of six 1,4-diazepanes prepared by condensation of 2,2′-(1,3-propanediyldiimino)diphenols with glyoxal or 2,3-butanedione to give bisbenzoxazolidines and subsequent reduction with BH3–DMS is reported.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::a4c5928f36c3110b98abcfed7daf6dc5
https://doi.org/10.1016/j.tetlet.2012.08.094
https://doi.org/10.1016/j.tetlet.2012.08.094
Autor:
María E. Ochoa, J. Manuel Méndez-Stivalet, Norberto Farfán, Braulio Rodríguez-Molina, Margarita Romero, Rosa Santillan, Miguel A. Garcia-Garibay, Pedro I. Ramirez-Montes, Rafael Arcos-Ramos
Publikováno v:
The Journal of organic chemistry. 77(16)
The search for voluminous stators that may accommodate large rotator units and speed rotational dynamics in the solid state led us to investigate a simple and efficient method for the synthesis of molecular rotors with tert-butyldiphenylsilyl-protect
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::2d88a92d921d6c916fd6b4fd65566905
https://pubmed.ncbi.nlm.nih.gov/22812677
https://pubmed.ncbi.nlm.nih.gov/22812677