Zobrazeno 1 - 6
of 6
pro vyhledávání: '"Soodabeh Forghani"'
Publikováno v:
ARKIVOC, Vol 2016, Iss 6, Pp 152-162 (2017)
Externí odkaz:
https://doaj.org/article/afa192cd80764aac8159dd949178886e
Autor:
Atefeh Hadizadeh, M. Saeed Abaee, Soodabeh Forghani, Fatemeh Ehteshami, Mohammad M. Mojtahedi
Publikováno v:
Journal of the Iranian Chemical Society. 14:1151-1157
1,3-Dithian-5-one 1 undergoes a convenient pseudo-four-component combination with different aldehydes 2 and two equivalents of malononitrile 3 in aqueous medium and in the presence of triethylamine. Novel dithian-fused dicyanoanilines 4 are formed ef
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::7aff7b77300b84c286104c245cfda7ab
https://doi.org/10.1007/s13738-017-1065-5
https://doi.org/10.1007/s13738-017-1065-5
Publikováno v:
Journal of Sulfur Chemistry. 37:259-268
In a mixture consisting of catalytic quantities of diethylamine, sodium dodecyl sulfate, and a zirconium salt in water, 2,2-dimethyl-1,3-dithian-5-one undergoes double aldol condensation with two folds of aromatic aldehydes at 50oC to yield the respe
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::770066168ddc9564a4ce34ebe5e8e20c
https://doi.org/10.1080/17415993.2015.1130131
https://doi.org/10.1080/17415993.2015.1130131
Autor:
M. Saeed Abaee, Somayeh Navidipoor, Soodabeh Forghani, Mohammad M. Mojtahedi, Somayeh Cheraghi
Publikováno v:
Tetrahedron Letters. 53:4405-4408
An efficient synthesis of β-aryl-β-mercapto ketones is achieved via a tandem aldol condensation-thia-Michael addition process using an aqueous medium and diethylamine. Addition of different thiols to α,β-unsaturated ketones, formed in situ from t
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::fb296d0d808aecdfd859ecb318bb1d6a
https://doi.org/10.1016/j.tetlet.2012.06.040
https://doi.org/10.1016/j.tetlet.2012.06.040
A facile procedure is developed for one-pot synthesis of a new group of dicyanoanilines. Tetrahydro-4H-thiopyran-4-one, 1, undergoes a pseudo four-component reaction with various aldehydes bearing different groups and two equivalents of malononitrile
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d6640733f9ed6f7c023b5897212caa75
Autor:
M. Saeed Abaee, Somayeh Cheraghi, Somayeh Navidipoor, Soodabeh Forghani, Mohammad M. Mojtahedi
Publikováno v:
ChemInform. 43
The condensation of acetophenone with aromatic aldehydes is followed by direct coupling of the resulting α,β-unsaturated ketones with thiols to afford the desired products within a short time and in a high yield.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::cf05896b5213935a5d741ca77fa95dcc
https://doi.org/10.1002/chin.201248066
https://doi.org/10.1002/chin.201248066