Literature DB >> 22091973

Synthesis of azines in solid state: reactivity of solid hydrazine with aldehydes and ketones.

Byeongno Lee1, Kyu Hyung Lee, Jaeheung Cho, Wonwoo Nam, Nam Hwi Hur.   

Abstract

Highly conjugated azines were prepared by solid state grinding of solid hydrazine and carbonyl compounds such as aldehydes and ketones, using a mortar and a pestle. Complete conversion to the azine product is generally achieved at room temperature within 24 h, without using solvents or additives. The solid-state reactions afford azines as the sole products with greater than 97% yield, producing only water and carbon dioxide as waste.

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Year:  2011        PMID: 22091973     DOI: 10.1021/ol202593g

Source DB:  PubMed          Journal:  Org Lett        ISSN: 1523-7052            Impact factor:   6.005


  2 in total

1.  Direct Synthesis of Symmetrical Azines from Alcohols and Hydrazine Catalyzed by a Ruthenium Pincer Complex: Effect of Hydrogen Bonding.

Authors:  Jonathan O Bauer; Gregory Leitus; Yehoshoa Ben-David; David Milstein
Journal:  ACS Catal       Date:  2016-11-17       Impact factor: 13.084

2.  N,N-disubstituted azines attenuate LPS-mediated neuroinflammation in microglia and neuronal apoptosis via inhibiting MAPK signaling pathways.

Authors:  Lalita Subedi; Oh Wook Kwon; Chaeho Pak; Goeun Lee; Kangwoo Lee; Hakwon Kim; Sun Yeou Kim
Journal:  BMC Neurosci       Date:  2017-12-28       Impact factor: 3.288

  2 in total

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