M
Majid Ghazanfarpour-Darjani
Researcher at Tarbiat Modares University
Publications - 38
Citations - 425
Majid Ghazanfarpour-Darjani is an academic researcher from Tarbiat Modares University. The author has contributed to research in topics: Aryl & Alkyl. The author has an hindex of 12, co-authored 38 publications receiving 386 citations. Previous affiliations of Majid Ghazanfarpour-Darjani include Islamic Azad University.
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Journal ArticleDOI
Methoxide Ion Promoted Efficient Synthesis of 1,3-Oxathiolane-2-thiones by Reaction of Oxiranes and Carbon Disulfide
Issa Yavari,Majid Ghazanfarpour-Darjani,Zinatossadat Hossaini,Maryam Sabbaghan,Nargess Hosseini +4 more
TL;DR: In this paper, an efficient one-pot synthesis of functionalized 1,3-oxathiolane-2-thiones was described via reaction of carbon disulfide with oxiranes in the presence of sodium hydride (10 mol%) and methanol.
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Reaction of N-Heterocycles with Acetylenedicarboxylates in the Presence of N-Alkylisatins or Ninhydrin. Efficient Synthesis of Spiro Compounds
TL;DR: In this article, the 1,3-dipolar intermediates generated by addition of isoquinoline, to dialkyl acetylenedicaboxylates are trapped by N-alkylisatins to produce dialkyyl 1,2-dihydro-2-oxo-1alkylspiro[3H-indol-3,2′-[2H,11bH][1,3]oxazino[2,3a]isoquinoline]-3′,4′-dicarboxylates in excellent
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Synthesis of dimethyl 1,2-dihydroisoquinolines through the reaction of isoquinoline and dimethyl acetylenedicarboxylate in the presence of amides
TL;DR: Isoquinoline reacts smoothly with dimethyl acetylenedicarboxylate (DMAD) in the presence of amides to produce dimethyl 2-[1]-aryl(alkyl)carbonylamino]-2(1H)-isoquinolinyl]-2-butenedioates as mentioned in this paper.
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Efficient synthesis of functionalized spiro-2,5-dihydro-1,2-λ5-oxaphospholes
TL;DR: In this paper, the reaction of dialkyl acetylenedicarboxylates with triphenylphosphine (Ph 3 P) in the presence of N -alkylisatins led to a good yield.
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Surprising Formation of Chlorinated Butenolides from Dialkyl Acetylenedicarboxylates and Hexachloroacetone in the Presence of Triphenyl Phosphite
TL;DR: Triphenyl phosphite reacts smoothly with dialkyl acetylenedicarboxylates and hexachloroacetone to produce alkyl 2-(dichloromethylene)-2,5-dihydro-5-oxo-4-(trichlormethyl)furan-3-carboxylate in good yields.