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  2. 2,3-Dichloro-5,6-dicyano-1,4-benzoquinone - Wikipedia

    en.wikipedia.org/wiki/2,3-Dichloro-5,6-dicyano-1...

    2,3-Dichloro-5,6-dicyano-1,4-benzoquinone (or DDQ) is the chemical reagent with formula C 6 Cl 2 (CN) 2 O 2. This oxidant is useful for the dehydrogenation of alcohols, [3] phenols, [4] and steroid ketones. [5] DDQ decomposes in water, but is stable in aqueous mineral acid. [6]

  3. Protecting group - Wikipedia

    en.wikipedia.org/wiki/Protecting_group

    The use of protective groups is pervasive but not without criticism. [103] In practical terms their use adds two steps (protection-deprotection sequence) to a synthesis, either or both of which can dramatically lower chemical yield. Crucially, added complexity impedes the use of synthetic total synthesis in drug discovery.

  4. File:PMB deprotection mechanismn.svg - Wikipedia

    en.wikipedia.org/wiki/File:PMB_deprotection...

    Main page; Contents; Current events; Random article; About Wikipedia; Contact us; Help; Learn to edit; Community portal; Recent changes; Upload file

  5. tert-Butyldiphenylsilyl - Wikipedia

    en.wikipedia.org/wiki/Tert-Butyldiphenylsilyl

    This might involve using the triflate or the less reactive chloride of TBDPS along with a mild base such as 2,6-lutidine or pyridine and potentially a catalyst such as DMAP or imidazole. [ 3 ] The ease of installation of the protecting group follows the order: 1 o > 2 o > 3 o , allowing the least hindered hydroxyl group to be protected in the ...

  6. SIESTA (computer program) - Wikipedia

    en.wikipedia.org/wiki/SIESTA_(computer_program)

    SIESTA (Spanish Initiative for Electronic Simulations with Thousands of Atoms) is an original method and its computer program implementation, to efficiently perform electronic structure calculations and ab initio molecular dynamics simulations of molecules and solids.

  7. Photolabile protecting group - Wikipedia

    en.wikipedia.org/wiki/Photolabile_protecting_group

    [1] [2] [3] Since their introduction in 1962, [4] numerous PPGs have been developed and utilized in a variety of wide-ranging applications from protein science [5] to photoresists. Due to the large number of reported protecting groups, PPGs are often categorized by their major functional group(s); three of the most common classifications are ...

  8. Trimethylsilylacetylene - Wikipedia

    en.wikipedia.org/wiki/Trimethylsilylacetylene

    Trimethylsilylacetylene is also used to synthesize diphenylacetylene derivatives in a one-pot Sonogashira coupling, in which the phenylacetylene derivative reacts with a second aryl halide after in-situ deprotection. [3] A less expensive alternative reagent is 2-methylbut-3-yn-2-ol, which after alkynylation is deprotected with base.

  9. List of software for nuclear engineering - Wikipedia

    en.wikipedia.org/wiki/List_of_software_for...

    Neutron kinetics, thermal-hydraulics, and structural mechanics are all important in this effort. Each software needs to be tested and verified before use. [1] The codes can be separated by use and function. Most of the software are written in C and Fortran. [2]