Page last updated: 2024-08-18

benzonitrile and iodine

benzonitrile has been researched along with iodine in 5 studies

Research

Studies (5)

TimeframeStudies, this research(%)All Research%
pre-19900 (0.00)18.7374
1990's0 (0.00)18.2507
2000's0 (0.00)29.6817
2010's5 (100.00)24.3611
2020's0 (0.00)2.80

Authors

AuthorsStudies
Fujita, T; Hashimoto, K; Kasashima, Y; Mino, T; Sakamoto, M; Uzawa, A; Yokoyama, Y1
Fujita, T; Hanzawa, Y; Kasashima, Y; Mino, T; Sakamoto, M; Tomono, K1
Hoz, S; Rao, CN1
Jiménez, C; Montaos, MA; Rodríguez, J; Segade, Y1
Khalaj, M; Nasrollahzadeh, M; Rostami-Vartooni, A; Sajadi, SM1

Other Studies

5 other study(ies) available for benzonitrile and iodine

ArticleYear
Amidation of alcohols with nitriles under solvent-free conditions using molecular iodine as a catalyst.
    Journal of oleo science, 2010, Volume: 59, Issue:11

    Topics: Amides; Benzyl Alcohols; Camphanes; Catalysis; Dehydration; Iodine; Nitriles; Organic Chemistry Phenomena; Solvents; Stereoisomerism; Temperature

2010
Amide synthesis from esters with nitriles under solvent-free conditions using molecular iodine as a catalyst.
    Journal of oleo science, 2012, Volume: 61, Issue:7

    Topics: Amides; Catalysis; Esters; Iodine; Nitriles; Phenylacetates; Solvents

2012
Synergism and inhibition in the combination of visible light and HMPA in SmI2 reductions.
    The Journal of organic chemistry, 2012, Oct-19, Volume: 77, Issue:20

    Topics: Acetylene; Benzoates; Hempa; Iodides; Light; Molecular Structure; Naphthalenes; Nitriles; Oxidation-Reduction; Samarium

2012
A short stereoselective synthesis of prepiscibactin using a SmI2-mediated Reformatsky reaction and Zn2+-induced asymmetric thiazolidine formation.
    Organic letters, 2014, Nov-07, Volume: 16, Issue:21

    Topics: Animals; Cysteine; Fish Diseases; Fishes; Iodides; Molecular Structure; Nitriles; Pasteurella Infections; Pfiesteria piscicida; Photobacterium; Samarium; Stereoisomerism; Thiazoles; Thiazolidines; Zinc

2014
Natrolite zeolite supported copper nanoparticles as an efficient heterogeneous catalyst for the 1,3-diploar cycloaddition and cyanation of aryl iodides under ligand-free conditions.
    Journal of colloid and interface science, 2015, Sep-01, Volume: 453

    Topics: Catalysis; Copper; Cycloaddition Reaction; Green Chemistry Technology; Iodides; Ligands; Nanoparticles; Nitriles; Silicates; Triazoles; Zeolites

2015