Jove
Visualize
Contact Us
JoVE
x logofacebook logolinkedin logoyoutube logo
ABOUT JoVE
OverviewLeadershipBlogJoVE Help Center
AUTHORS
Publishing ProcessEditorial BoardScope & PoliciesPeer ReviewFAQSubmit
LIBRARIANS
TestimonialsSubscriptionsAccessResourcesLibrary Advisory BoardFAQ
RESEARCH
JoVE JournalMethods CollectionsJoVE Encyclopedia of ExperimentsArchive
EDUCATION
JoVE CoreJoVE BusinessJoVE Science EducationJoVE Lab ManualFaculty Resource CenterFaculty Site
Terms & Conditions of Use
Privacy Policy
Policies

Related Experiment Videos

Solution-phase combinatorial chemistry.

D M Coe1, R Storer

  • 1Glaxo Wellcome Research and Development, Medicines Research Centre, Stevenage, U.K.

Molecular Diversity
|May 13, 1999
PubMed
Summary
This summary is machine-generated.

Related Concept Videos

You might also read

Related Articles

Articles linked to this work by shared authors, journal, and citation graph.

Sort by
Same author

Synthesis of 2'-C-methyl-4'-thio ribonucleosides.

Nucleosides, nucleotides & nucleic acids·2005
Same author

Synthesis of 2'-C-methyl-beta-D-ribofuranosylimidazo [4,5-d]-pyridazine derivatives (2-aza-3-deazapurine nucleoside analogues).

Nucleosides, nucleotides & nucleic acids·2005
Same author

Synthesis of 5-aza-7-deazaguanine nucleoside derivatives as potential anti-flavivirus agents.

Nucleosides, nucleotides & nucleic acids·2005
Same author

Rapid access to 2'-branched-carbocyclic nucleosides and their 4'-epimers from 2-alkyl-cyclopentene-1-ones.

Nucleosides, nucleotides & nucleic acids·2005
Same author

Nm 283, an efficient prodrug of the potent anti-HCV agent 2'-C-methylcytidine.

Nucleosides, nucleotides & nucleic acids·2005
Same author

Effect of an internal rotating current on low-frequency inductively coupled plasmas.

Physical review. E, Statistical, nonlinear, and soft matter physics·2001

Solution-phase chemistry offers an alternative to solid-phase methods for preparing compound arrays in drug discovery. Recent advances, including supported reagents and extractive protocols, improve the quality of samples despite purification challenges.

Area of Science:

  • Medicinal Chemistry
  • Synthetic Chemistry
  • Drug Discovery

Background:

  • Solid-phase chemistry is a common approach for preparing compound arrays.
  • Solution-phase techniques present an alternative with different advantages and disadvantages.
  • Purification remains a key challenge in solution-phase synthesis.

Purpose of the Study:

  • To explore solution-phase techniques as an alternative to solid-phase chemistry for compound array preparation.
  • To highlight recent advancements in solution-phase array chemistry.
  • To demonstrate methods for preparing high-quality samples using solution-phase approaches.

Main Methods:

  • Utilizing supported reagents in solution-phase reactions.
  • Implementing simple extractive protocols for purification.

Related Experiment Videos

  • Preparing arrays of compounds via solution-phase synthesis.
  • Main Results:

    • Solution-phase techniques can overcome some limitations of solid-phase methods.
    • Supported reagents and extractive protocols facilitate the preparation of high-quality samples.
    • Effective sample preparation is achievable despite inherent purification challenges.

    Conclusions:

    • Solution-phase array chemistry is a viable and advancing field for drug discovery.
    • Recent innovations enhance the efficiency and quality of solution-phase compound preparation.
    • Further development in purification strategies will strengthen solution-phase approaches.