Zobrazeno 1 - 10
of 33
pro vyhledávání: '"Baris Temelli"'
Autor:
Baris Temelli, Pinar Kapci
Publikováno v:
Beilstein Journal of Organic Chemistry, Vol 18, Iss 1, Pp 1403-1409 (2022)
A copper triflate-mediated approach to access copper complexes of pyrrole-substituted corroles from the reaction of 1,9-diformyldipyrromethanes and an excess amount of pyrrole is presented for the first time. This procedure is a simple and efficient
Externí odkaz:
https://doaj.org/article/9a1cd16695f243819bdefbeab9e33798
Autor:
Baris Temelli, Hilal Kalkan
Publikováno v:
Beilstein Journal of Organic Chemistry, Vol 14, Iss 1, Pp 187-193 (2018)
The preparation of β-meso directly linked porphyrin–corrole hybrids was realized for the first time via an InCl3-catalyzed condensation reaction of 2-formyl-5,10,15,20-tetraphenylporphyrins with meso-substituted dipyrromethanes. Hybrid compounds h
Externí odkaz:
https://doaj.org/article/d9f40641b721498bbae94cc8591681a9
Autor:
Baris, Temelli, Pinar, Kapci
Publikováno v:
Beilstein journal of organic chemistry. 18
A copper triflate-mediated approach to access copper complexes of pyrrole-substituted corroles from the reaction of 1,9-diformyldipyrromethanes and an excess amount of pyrrole is presented for the first time. This procedure is a simple and efficient
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::1d8bd416050b1adb39390bbe7afb8267
https://pubmed.ncbi.nlm.nih.gov/36262669
https://pubmed.ncbi.nlm.nih.gov/36262669
Publikováno v:
Tetrahedron. 74:4476-4488
Ethynyl-bridged porphyrin-corrole dyads and triads were synthesized by using Pd(0) mediated coupling reactions and their structures were characterized by NMR, FT-IR, UV/Vis and fluorescence techniques. Besides spectroscopic techniques, computational
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::30ca4e69e10e3d47bae4d631de57080a
https://doi.org/10.1016/j.tet.2018.07.007
https://doi.org/10.1016/j.tet.2018.07.007
Autor:
Baris Temelli, Hilal Kalkan
Publikováno v:
Synthetic Communications. 48:2112-2117
Unexpected formation of β, meso-directly linked diporphyrin products has been described in the reactions of β-formyl porphyrins with pyrrole under Adler–Longo reaction conditions. Preliminary mechanistic studies indicates that β-dipyrromethane s
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::19abdf364af046eac08e26ceacec56f1
https://doi.org/10.1080/00397911.2018.1486426
https://doi.org/10.1080/00397911.2018.1486426
Publikováno v:
European Journal of Organic Chemistry. 2017:4905-4915
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::b2730ee560c6daafc856d23becb5ef9e
https://doi.org/10.1002/ejoc.201700896
https://doi.org/10.1002/ejoc.201700896
Publikováno v:
European Journal of Organic Chemistry. 2015:7583-7593
A new, catalytic, and general methodology was developed for the direct synthesis of unsymmetrical AB-type tripyrranes by reaction of dipyrromethanesulfonamides with pyrrole. Key structure dipyrromethanesulfonamides were synthesized by the addition of
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::b9191327bc600048378ecce99f9bf9ce
https://doi.org/10.1002/ejoc.201501062
https://doi.org/10.1002/ejoc.201501062
Publikováno v:
Polymer Bulletin. 72:867-879
In this work, electropolymerization of 5-phenyl dipyrromethane (DPM) and electrochemical behavior of the obtained polymer were performed. The monomer was electropolymerized in a solution of DPM and 0.1 M tetra-n-butyl ammonium perchlorate/dichloromet
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::16d434f5b3eb912765f21a553c8915f4
https://doi.org/10.1007/s00289-015-1311-x
https://doi.org/10.1007/s00289-015-1311-x
Autor:
Canan Unaleroglu, Baris Temelli
Publikováno v:
Synthesis. 46:1407-1412
A new and practical direct transformation of primary nitro compounds into nitriles with sodium dithionite is described. The reaction is simple, convenient and eliminates the use of expensive and moisture-sensitive reagents.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::062b3763faf69ac35d2407a8e6abc7e2
https://doi.org/10.1055/s-0033-1370874
https://doi.org/10.1055/s-0033-1370874
Publikováno v:
Tetrahedron Letters. 55:544-547
The selective synthesis of [26]hexaphyrin(1.1.1.1.1.1) has been achieved by the reaction of meso-substituted tripyrrane and N-sulfonyl aldimine. The protocol is simple and requires only a catalytic amount of copper(II) triflate under mild reaction co
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::9480d95b2ec72bf562d0a8fbff07185b
https://doi.org/10.1016/j.tetlet.2013.11.101
https://doi.org/10.1016/j.tetlet.2013.11.101