Zobrazeno 1 - 10
of 52
pro vyhledávání: '"Saber, Mirzaei"'
Autor:
Saber Mirzaei, Seyed, Mehrdadi, Nasser, Nabi bidhendi, Gholamreza, Pourmadadi, Mehrab, Ahmadi, Mohammadjavad, Meknatkhah, Sogol
Publikováno v:
In Microchemical Journal May 2024 200
Autor:
Saber Mirzaei, Seyed, Mehrdadi, Nasser, Nabi bidhendi, Gholamreza, Pourmadadi, Mehrab, Ahmadi, Mohammadjavad, Meknatkhah, Sogol
Publikováno v:
In Microchemical Journal September 2024 204
Publikováno v:
Chemical Science. 13:2026-2032
Macrocyclic arenes laid the foundations of supramolecular chemistry and their study established the fundamentals of noncovalent interactions. Advancing their frontier, here we designed rigidified resorcin[4]arenes that serve as hosts for large nonsph
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::997ae472c7c5e431487abc56e42d502b
https://doi.org/10.1039/d1sc07041j
https://doi.org/10.1039/d1sc07041j
Publikováno v:
Green Chemistry. 24:9069-9083
Naturally sourced 2-picolinic acid was discovered as an off-the-shelf, non-toxic, and inexpensive HBD catalyst for the cycloaddition of CO2 to both internal and terminal epoxides to prepare cyclic carbonates at low catalyst loadings.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::d850c73e4f65f9081e93df36a131a1ea
https://doi.org/10.1039/d2gc02146c
https://doi.org/10.1039/d2gc02146c
Publikováno v:
ACS Catalysis. 11:14570-14574
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::9ea88caa70a23aef54d9a3a3654393ed
https://doi.org/10.1021/acscatal.1c04743
https://doi.org/10.1021/acscatal.1c04743
Autor:
Saber Mirzaei, Hormoz Khosravi, Kamran Amiri, Dmitry Dar'in, Hamid Reza Bijanzadeh, Saeed Balalaie, Frank Rominger, Behrouz Nayebzadeh, Mikhail Krasavin
Publikováno v:
The Journal of Organic Chemistry. 86:13693-13701
A transition-metal-free postmodification of the Groebke-Blackburn-Bienayme (GBB) reaction for the synthesis of spiro[chromene-imidazo[1,2-a]pyridin]-3'-imine was discovered. The unusual transformation represents the first example of activation and th
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::08b9345f861ad8ddd5ed4ccd2a00932c
https://doi.org/10.1021/acs.joc.1c01789
https://doi.org/10.1021/acs.joc.1c01789
Autor:
Manasseh Kusi Osei, Saber Mirzaei, Xiaowei Bogetti, Edison Castro, Mohammad Azizur Rahman, Sunil Saxena, Raúl Hernández Sánchez
Publikováno v:
Angewandte Chemie. 134
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::0856083ca405dec6c430899c11c6ce1f
https://doi.org/10.1002/ange.202209529
https://doi.org/10.1002/ange.202209529
Publikováno v:
The Journal of organic chemistry. 87(15)
We employed density functional theory (DFT) methods to investigate the most plausible mechanism of cyclization/ring expansion of proline with
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::cd5d9464b5daa4560b779a34e86e0e88
https://pubmed.ncbi.nlm.nih.gov/35816612
https://pubmed.ncbi.nlm.nih.gov/35816612
Publikováno v:
Chemistry – A European Journal. 27:8642-8655
Molecular compounds with permanent tubular architectures displaying radial π-conjugation are exceedingly rare. Their radial and axial delocalization presents them with unique optical and electronic properties, such as remarkable tuning of their Stok
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f364c57141fffd6dce57edfc13e44348
https://doi.org/10.1002/chem.202005408
https://doi.org/10.1002/chem.202005408
Publikováno v:
Chemical Research in Toxicology. 34:959-987
Mechanism-based inactivation (MBI) refers to the metabolic bioactivation of a xenobiotic by cytochrome P450s to a highly reactive intermediate which subsequently binds to the enzyme and leads to the quasi-irreversible or irreversible inhibition. Xeno
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::33eab50b4d8c82b778907a9c0f2664f0
https://doi.org/10.1021/acs.chemrestox.0c00483
https://doi.org/10.1021/acs.chemrestox.0c00483