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  • 2018
  • 4-(4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-yl)-isoquinoline (CAS 685103-98-4) Market Research Report 2018 contents were worked out and placed on the website in February, 2018. (marketpublishers.com)
  • Please note that 4-(4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-yl)-isoquinoline (CAS 685103-98-4) Market Research Report 2018 is a half ready publication and contents are subject to change. (marketpublishers.com)
  • Molecular
  • A molecular scaffold that integrates both isoquinoline and benzimidazole subunits, such as fused benzimidazoisoquinoline rings, has an immense potential due to outstanding biological and pharmacological activities, such as anti-HIV-1, anticancer, antimicrobial, and antifungal properties. (rsc.org)
  • Early cell culture studies have provided convincing evidence of isoquinoline neurotoxicity.22,23 More recent studies have explored mechanisms of dopaminergic cell death produced by TIQs using both molecular and morphological assays. (alpfmedical.info)
  • wide range
  • In our method, lithiated o-tolualdehyde tert-butylimines were condensed with different nitriles to generate eneamido anion intermediates, which were trapped in situ with various electrophiles at the C4-position, affording a wide range of substituted isoquinolines. (harvard.edu)
  • found
  • Furthermore, 4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-isoquinoline prices in regional markets can be found in the report with regards to countries and companies. (marketpublishers.com)
  • method
  • This method provides a convenient, room temperature, atom-economical, and catalyst-free access to diversely substituted isoquinoline fused benzimidazoles. (rsc.org)
  • introduction
  • In our synthesis, we envisioned that natural cortistatins and unnatural analogs could be prepared by late-stage introduction of isoquinolines to 17-keto precursors, and that these differentially substituted precursors could all be derived from a common key intermediate 112. (harvard.edu)