Zobrazeno 1 - 10
of 30
pro vyhledávání: '"Jamaleddini, A."'
Autor:
Seyedeh Hekmat Mousavi, Mohammad Reza Mohammadizadeh, Zohreh Roshan, Azar Jamaleddini, Satoru Arimitsu
Publikováno v:
ACS Omega, Vol 5, Iss 29, Pp 18273-18288 (2020)
Externí odkaz:
https://doaj.org/article/32b7a57e45964ebbaaec013fcaf83aad
Autor:
Fooladsaz, Koorosh, Negahdary, Masoud *, Rahimi, Ghasem, Habibi-Tamijani, Amir, Parsania, Sara, Akbari-dastjerdi, Hajar, Sayad, Arezou, Jamaleddini, Azar, Salahi, Fatemeh, Asadi, Asadollah
Publikováno v:
In International Journal of Electrochemical Science October 2012 7(10):9892-9908
Autor:
Negahdary, Masoud, Asadi, Asadollah, Mehrtashfar, Shokoufeh, Imandar, Mojtaba, Akbari-dastjerdi, Hajar, Salahi, Fatemeh, Jamaleddini, Azar, Ajdary, Marziyeh
Publikováno v:
In International Journal of Electrochemical Science 2012 7(6):5185-5194
Autor:
Satoru Arimitsu, Zohreh Roshan, Azar Jamaleddini, Mohammad Reza Mohammadizadeh, Seyedeh Hekmat Mousavi
Publikováno v:
ACS Omega
ACS Omega, Vol 5, Iss 29, Pp 18273-18288 (2020)
ACS Omega, Vol 5, Iss 29, Pp 18273-18288 (2020)
A one-pot route for the synthesis of spiro-isobenzofuran compounds was developed via the condensation reaction of ninhydrin with 4-amino-1,2-naphthoquinones or 2-amino-1,4-naphthoquinones in acetic acid followed by the oxidative cleavage of the corre
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a1d40246411cce0cb9add4887edb8b1f
http://europepmc.org/articles/PMC7392522
http://europepmc.org/articles/PMC7392522
Akademický článek
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Publikováno v:
Tetrahedron Letters. 58:78-81
The oxidation of 3a,8a-dihydroxy-2-(alkyl/benzylthio)indeno[1,2-d]imidazol-8(3H)-ones to give the corresponding 3-(alkyl/benzylthio)-9b-hydroxy-1H-imidazo[5,1-a]isoindole-1,5(9bH)-dione derivatives in good to excellent yields at room temperature usin
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::c0ea051bb379586693e377c72ed7e9b1
https://doi.org/10.1016/j.tetlet.2016.11.109
https://doi.org/10.1016/j.tetlet.2016.11.109
Publikováno v:
In Tetrahedron Letters 4 January 2017 58(1):78-81
Publikováno v:
Journal of Sulfur Chemistry. 34:259-263
Deoxygenation of structurally diverse sulfoxides including dialkyl, diaryl, aryl alkyl and allyl sulfoxides to the corresponding sulfides were carried out using a NaI/silica sulfuric acid reducing system at room temperature in poly ethylene glycol (P
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::5a71706ad071ca6723d319a1b9810ce4
https://doi.org/10.1080/17415993.2012.733005
https://doi.org/10.1080/17415993.2012.733005
Publikováno v:
Journal of Sulfur Chemistry. 33:413-418
An effective procedure for deoxygenation of sulfoxides to sulfides using thioacetic acid as a reducing agent and a catalytic amount of I2 in MeCN at ambient temperature has been developed. Using this protocol, a variety of sulfoxides including benzyl
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::f8e9a5bcd3950d0cf2a899e3f40837e0
https://doi.org/10.1080/17415993.2012.693491
https://doi.org/10.1080/17415993.2012.693491
Akademický článek
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