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Peyman Salehi

Researcher at Shahid Beheshti University

Publications -  317
Citations -  6863

Peyman Salehi is an academic researcher from Shahid Beheshti University. The author has contributed to research in topics: Catalysis & Essential oil. The author has an hindex of 41, co-authored 309 publications receiving 6112 citations. Previous affiliations of Peyman Salehi include University of Gilan & University of Isfahan.

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Essential oil composition and antioxidant activity of different extracts of Nepeta betonicifolia C.A. Meyer and Nepeta saccharata Bunge.

TL;DR: The antioxidant activity of the butanolic subfractions of both plants was higher than other extracts examined, and the radical scavenging capacity (RSC) of methanol extracts and chloroform, butanol and water subfraction of aerial parts of N. betonicifolia and N. saccharata was high.
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An Efficient One‐Pot, Four‐Component Synthesis of {[(1H‐1,2,3‐Triazol‐4‐yl)methoxy]phenyl}‐1H‐pyrazolo[1,2‐b]phthalazine‐5,10‐dione Derivatives

TL;DR: In this paper, the 1-1H-1,2,3-Triazol-4-yl)methoxy derivatives were synthesized by a simple and efficient method, i.e., by the four-component, one-pot condensation reaction of phthalohydrazide 4, a (propargyloxy)benzaldehyde 1, an active methylene compound 3 (malononitrile or ethyl cyanoacetate), and an azide 2 in the presence of Cu(OAc)2/sodium L-ascorb
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Antiprotozoal Isoprenoids from Salvia hydrangea

TL;DR: Fractionation of the n-hexane extract of Salvia hydrangea afforded seven isoprenoids including six new compounds (1-6) and salvadione A (7) and a biosynthetic pathway for the formation of the scaffold of 1 is proposed.
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N-substituted noscapine derivatives as new antiprotozoal agents: Synthesis, antiparasitic activity and molecular docking study.

TL;DR: Novel N-substituted noscapine derivatives were synthesized by a three-component Strecker reaction of cyclic ether of N-nornoscapine with varied aldehydes, in the presence of cyanide ion in good yields.
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An efficient method for catalytic enantioselective addition of diethylzinc to aryl aldehydes by a C2-symmetric chiral imino alcohol

TL;DR: In this paper, the enantioselective alkylation of aryl aldehydes with diethylzinc in the presence of a C2-symmetric chiral ligand derived from 2-hydroxy-3-pinanone was achieved at room temperature with high enantiomeric excesses.